Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1106 |
| ensemblid | ENSG00000173575.24 |
| hgncid | 1917 |
| symbol | CHD2 |
| name | chromodomain helicase DNA binding protein 2 |
| refseq_nuc | NM_001271.4 |
| refseq_prot | NP_001262.3 |
| ensembl_nuc | ENST00000394196.9 |
| ensembl_prot | ENSP00000377747.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 92900324 |
| end | 93027996 |
| strand | + |
| ver | v1.2 |
| region | chr15:92900324-93027996 |
| region5000 | chr15:92895324-93032996 |
| regionname0 | CHD2_chr15_92900324_93027996 |
| regionname5000 | CHD2_chr15_92895324_93032996 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 5484 | 163 | 16 | 45 | 72 | 7 | 23 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0002 | 0/0 | 5484 | 47 | 14 | 7 | 24 | 1 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0003 | 1/0 | 5484 | 38 | 23 | 9 | 0 | 0 | 5 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0004 | 0/0 | 5484 | 18 | 2 | 5 | 7 | 1 | 3 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0005 | 0/0 | 5484 | 12 | 1 | 3 | 0 | 6 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0006 | 0/0 | 5484 | 5 | 3 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0007 | 0/0 | 5484 | 4 | 3 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0008 | 0/1 | 5484 | 3 | 1 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0009 | 0/0 | 5484 | 3 | 2 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0010 | 0/0 | 5484 | 2 | 2 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0011 | 0/0 | 5484 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0012 | 0/0 | 5484 | 2 | 2 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0013 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0014 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0015 | 0/0 | 5484 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0016 | 0/0 | 5484 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0017 | 0/0 | 5484 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0018 | 0/0 | 5484 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 | ||
| a0001c0019 | 0/0 | 5484 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | ATGAT others(5479): Show |
chr15 | 92895324 | 93032996 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9353 | 121 | 8 | 29 | 61 | 5 | 18 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0002 | 0/0 | 9350 | 6 | 4 | 0 | 1 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0003 | 0/0 | 9350 | 3 | 1 | 0 | 0 | 2 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0005 | 0/0 | 9353 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0006 | 0/0 | 9350 | 14 | 1 | 12 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0007 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0008 | 0/0 | 9353 | 4 | 0 | 0 | 0 | 0 | 4 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0009 | 0/0 | 9353 | 4 | 0 | 1 | 3 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0011 | 0/0 | 9353 | 3 | 0 | 2 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0020 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0021 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0022 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0023 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0024 | 0/0 | 9353 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0001t0025 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0002t0001 | 0/0 | 9353 | 23 | 0 | 1 | 21 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0002t0002 | 0/0 | 9350 | 8 | 7 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0002t0003 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0002t0005 | 0/0 | 9353 | 8 | 6 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0002t0008 | 0/0 | 9353 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0002t0009 | 0/0 | 9353 | 2 | 0 | 1 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0002t0011 | 0/0 | 9353 | 2 | 0 | 0 | 2 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0002t0016 | 0/0 | 9350 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0003t0001 | 0/0 | 9353 | 4 | 1 | 1 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0003t0002 | 0/0 | 9350 | 5 | 4 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0003t0003 | 1/0 | 9350 | 20 | 14 | 4 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0003t0005 | 0/0 | 9353 | 3 | 3 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0003t0008 | 0/0 | 9353 | 2 | 0 | 1 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0003t0012 | 0/0 | 9350 | 3 | 0 | 2 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0003t0014 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0004t0004 | 0/0 | 9347 | 4 | 0 | 0 | 1 | 0 | 3 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9342): Show |
chr15 | 92895324 | 93032996 |
| a0001c0004t0007 | 0/0 | 9350 | 6 | 1 | 4 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0004t0010 | 0/0 | 9350 | 6 | 0 | 0 | 6 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0004t0017 | 0/0 | 9350 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0004t0018 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0005t0004 | 0/0 | 9347 | 9 | 1 | 2 | 0 | 4 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9342): Show |
chr15 | 92895324 | 93032996 |
| a0001c0005t0007 | 0/0 | 9350 | 2 | 0 | 0 | 0 | 2 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0005t0015 | 0/0 | 9347 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9342): Show |
chr15 | 92895324 | 93032996 |
| a0001c0006t0004 | 0/0 | 9347 | 4 | 2 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9342): Show |
chr15 | 92895324 | 93032996 |
| a0001c0006t0005 | 0/0 | 9353 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0007t0003 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0007t0007 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0007t0013 | 0/0 | 9350 | 2 | 1 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0008t0001 | 0/1 | 9353 | 3 | 1 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0009t0002 | 0/0 | 9350 | 2 | 1 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0009t0012 | 0/0 | 9350 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0010t0002 | 0/0 | 9350 | 2 | 2 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0011t0001 | 0/0 | 9353 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0012t0002 | 0/0 | 9350 | 2 | 2 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0013t0019 | 0/0 | 9353 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0014t0005 | 0/0 | 9353 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0015t0005 | 0/0 | 9353 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0016t0002 | 0/0 | 9350 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9345): Show |
chr15 | 92895324 | 93032996 |
| a0001c0017t0009 | 0/0 | 9353 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0018t0009 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| a0001c0019t0001 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | AGAGC others(9348): Show |
chr15 | 92895324 | 93032996 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0008g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0008g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0008g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0009g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0009g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0009g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0011g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0011g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0011g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0020g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0021g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0022g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0023g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0024g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0001t0025g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0008g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0008g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0009g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0009g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0011g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0011g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0002t0016g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0138 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0008g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0008g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0012g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0012g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0012g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0003t0014g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0004g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0004g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0007g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0010g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0017g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0004t0018g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0007g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0005t0015g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0006t0004g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0006t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0006t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0006t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0007t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0007t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0007t0013g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0007t0013g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0008t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0008t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0008t0001g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0009t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0009t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0009t0012g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0010t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0010t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0011t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0011t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0012t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0012t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0013t0019g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0014t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0015t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0016t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0017t0009g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0018t0009g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| a0001c0019t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0005 | t0007 | g0050 | EUR | GBR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00099 | hp2 | a0001 | c0002 | t0016 | g0280 | EUR | GBR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00140 | hp1 | a0001 | c0005 | t0007 | g0090 | EUR | GBR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00140 | hp2 | a0001 | c0005 | t0004 | g0180 | EUR | GBR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00323 | hp2 | a0001 | c0008 | t0001 | g0127 | EUR | FIN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00621 | hp1 | a0001 | c0001 | t0020 | g0113 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00621 | hp2 | a0001 | c0001 | t0025 | g0104 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00639 | hp1 | a0001 | c0004 | t0007 | g0014 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00639 | hp2 | a0001 | c0011 | t0001 | g0023 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00642 | hp1 | a0001 | c0016 | t0002 | g0047 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00673 | hp2 | a0001 | c0009 | t0002 | g0048 | EAS | CHS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0296 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0263 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00738 | hp1 | a0001 | c0011 | t0001 | g0024 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00738 | hp2 | a0001 | c0005 | t0004 | g0287 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00741 | hp1 | a0001 | c0002 | t0008 | g0012 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0134 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01069 | hp1 | a0001 | c0005 | t0004 | g0159 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01069 | hp2 | a0001 | c0003 | t0002 | g0125 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01070 | hp1 | a0001 | c0003 | t0003 | g0175 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01070 | hp2 | a0001 | c0002 | t0008 | g0015 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0282 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01081 | hp1 | a0001 | c0005 | t0015 | g0075 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0262 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0261 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01109 | hp2 | a0001 | c0003 | t0003 | g0171 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01167 | hp2 | a0001 | c0002 | t0005 | g0279 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01168 | hp2 | a0001 | c0004 | t0007 | g0020 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01169 | hp2 | a0001 | c0002 | t0005 | g0277 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01175 | hp1 | a0001 | c0001 | t0011 | g0292 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01192 | hp1 | a0001 | c0017 | t0009 | g0038 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01243 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01243 | hp2 | a0001 | c0007 | t0013 | g0151 | AMR | PUR | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0266 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01257 | hp1 | a0001 | c0003 | t0012 | g0126 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01257 | hp2 | a0001 | c0001 | t0024 | g0074 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01258 | hp1 | a0001 | c0003 | t0012 | g0132 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0128 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01361 | hp1 | a0001 | c0002 | t0009 | g0022 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01433 | hp2 | a0001 | c0004 | t0007 | g0021 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0265 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01515 | hp1 | a0001 | c0005 | t0004 | g0289 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01517 | hp2 | a0001 | c0005 | t0004 | g0276 | EUR | IBS | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01884 | hp1 | a0001 | c0003 | t0005 | g0160 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0228 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0253 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01952 | hp2 | a0001 | c0003 | t0008 | g0140 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0275 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02004 | hp1 | a0001 | c0004 | t0007 | g0018 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0084 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02027 | hp2 | a0001 | c0001 | t0021 | g0076 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02040 | hp1 | a0001 | c0002 | t0009 | g0243 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0174 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02055 | hp2 | a0001 | c0003 | t0003 | g0161 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0254 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02148 | hp1 | a0001 | c0001 | t0006 | g0080 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0268 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CDX | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02257 | hp2 | a0001 | c0002 | t0005 | g0230 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02258 | hp1 | a0001 | c0009 | t0012 | g0043 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02273 | hp1 | a0001 | c0001 | t0006 | g0267 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02280 | hp1 | a0001 | c0012 | t0002 | g0055 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02280 | hp2 | a0001 | c0015 | t0005 | g0288 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0260 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0264 | AMR | PEL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02451 | hp1 | a0001 | c0004 | t0007 | g0013 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0227 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02572 | hp1 | a0001 | c0002 | t0005 | g0229 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0223 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02630 | hp1 | a0001 | c0007 | t0007 | g0030 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02630 | hp2 | a0001 | c0006 | t0004 | g0163 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02683 | hp1 | a0001 | c0003 | t0003 | g0142 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0144 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02717 | hp1 | a0001 | c0009 | t0002 | g0044 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02735 | hp2 | a0001 | c0003 | t0012 | g0131 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02809 | hp1 | a0001 | c0014 | t0005 | g0226 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02809 | hp2 | a0001 | c0003 | t0005 | g0166 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02886 | hp1 | a0001 | c0003 | t0003 | g0149 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02886 | hp2 | a0001 | c0004 | t0018 | g0025 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02922 | hp1 | a0001 | c0003 | t0005 | g0124 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02922 | hp2 | a0001 | c0012 | t0002 | g0031 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02970 | hp1 | a0001 | c0003 | t0003 | g0135 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02970 | hp2 | a0001 | c0010 | t0002 | g0222 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02976 | hp1 | a0001 | c0003 | t0003 | g0137 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0156 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0136 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0170 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03098 | hp1 | a0001 | c0003 | t0002 | g0221 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03098 | hp2 | a0001 | c0003 | t0003 | g0173 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03130 | hp1 | a0001 | c0006 | t0004 | g0158 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03130 | hp2 | a0001 | c0003 | t0003 | g0167 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0152 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03195 | hp2 | a0001 | c0006 | t0005 | g0133 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0224 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03209 | hp2 | a0001 | c0003 | t0003 | g0164 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0003 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03225 | hp2 | a0001 | c0007 | t0003 | g0157 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03239 | hp2 | a0001 | c0001 | t0008 | g0219 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0181 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03486 | hp1 | a0001 | c0007 | t0013 | g0150 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0220 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03490 | hp1 | a0001 | c0006 | t0004 | g0004 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03490 | hp2 | a0001 | c0005 | t0004 | g0291 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03492 | hp1 | a0001 | c0006 | t0004 | g0004 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0139 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | ESN | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0162 | AFR | GWD | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0129 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0290 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03669 | hp2 | a0001 | c0004 | t0004 | g0284 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03688 | hp1 | a0001 | c0004 | t0004 | g0297 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03688 | hp2 | a0001 | c0001 | t0008 | g0218 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03710 | hp1 | a0001 | c0004 | t0004 | g0285 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03831 | hp2 | a0001 | c0005 | t0004 | g0283 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0141 | SAS | BEB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04115 | hp1 | a0001 | c0001 | t0008 | g0040 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0217 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04228 | hp1 | a0001 | c0003 | t0008 | g0146 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18612 | hp1 | a0001 | c0001 | t0023 | g0052 | EAS | CHB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18612 | hp2 | a0001 | c0004 | t0010 | g0107 | EAS | CHB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0045 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18906 | hp2 | a0001 | c0003 | t0014 | g0165 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18952 | hp1 | a0001 | c0004 | t0010 | g0108 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18956 | hp1 | a0001 | c0004 | t0010 | g0245 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0269 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18963 | hp2 | a0001 | c0018 | t0009 | g0036 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18967 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18979 | hp2 | a0001 | c0004 | t0004 | g0092 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18993 | hp1 | a0001 | c0001 | t0011 | g0176 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA18994 | hp2 | a0001 | c0001 | t0009 | g0009 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19000 | hp1 | a0001 | c0019 | t0001 | g0119 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19000 | hp2 | a0001 | c0002 | t0011 | g0257 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19007 | hp1 | a0001 | c0002 | t0011 | g0256 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19043 | hp2 | a0001 | c0013 | t0019 | g0168 | AFR | LWK | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19065 | hp2 | a0001 | c0001 | t0009 | g0010 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19068 | hp1 | a0001 | c0001 | t0022 | g0097 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19083 | hp1 | a0001 | c0004 | t0010 | g0105 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19085 | hp2 | a0001 | c0004 | t0010 | g0109 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19088 | hp2 | a0001 | c0004 | t0010 | g0106 | EAS | JPT | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0169 | AFR | YRI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0172 | AFR | ASW | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20129 | hp2 | a0001 | c0002 | t0005 | g0225 | AFR | ASW | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | TSI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20752 | hp2 | a0001 | c0005 | t0004 | g0153 | EUR | TSI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | TSI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20805 | hp2 | a0001 | c0004 | t0007 | g0017 | EUR | TSI | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01123 | hp1 | a0001 | c0004 | t0017 | g0019 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02486 | hp1 | a0001 | c0008 | t0001 | g0145 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG02486 | hp2 | a0001 | c0010 | t0002 | g0182 | AFR | ACB | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | MSL | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20300 | hp1 | a0001 | c0003 | t0003 | g0147 | AFR | USA | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | USA | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0179 | AFR | LWK | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| NA21309 | hp2 | a0001 | c0005 | t0004 | g0154 | AFR | LWK | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| homoSapiens | chm13v2 | a0001 | c0008 | t0001 | g0148 | REF | REF | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0003 | g0138 | REF | REF | CHD2_chr15_92895324_93032996 | CHD2 | chr15 | 92895324 | 93032996 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92924411 | C | T | 1 | a0001c0019 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.153C>T | p.Ser51Ser | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/39 | 725/9350 | 153/5487 | 51/1828 | chr15 | 92924411 | |||
| chr15:92927279 | G | A | 1 | a0001c0010 | 2 | HG02486.hp2 HG02970.hp2 |
synonymous_variant | LOW | c.330G>A | p.Arg110Arg | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/39 | 902/9350 | 330/5487 | 110/1828 | chr15 | 92927279 | |||
| chr15:92955491 | T | C | 1 | a0001c0011 | 2 | HG00639.hp2 HG00738.hp1 |
synonymous_variant | LOW | c.1788T>C | p.Tyr596Tyr | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 15/39 | 2360/9350 | 1788/5487 | 596/1828 | chr15 | 92955491 | |||
| chr15:92967373 | A | G | 13 | a0001c0001 a0001c0002 a0001c0004 others(10): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
synonymous_variant | LOW | c.2049A>G | p.Glu683Glu | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/39 | 2621/9350 | 2049/5487 | 683/1828 | chr15 | 92967373 | |||
| chr15:92971912 | A | G | 1 | a0001c0018 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.2337A>G | p.Gly779Gly | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 18/39 | 2909/9350 | 2337/5487 | 779/1828 | chr15 | 92971912 | |||
| chr15:92978374 | A | G | 12 | a0001c0001 a0001c0002 a0001c0004 others(9): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
synonymous_variant | LOW | c.2718A>G | p.Gln906Gln | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/39 | 3290/9350 | 2718/5487 | 906/1828 | chr15 | 92978374 | |||
| chr15:92984389 | C | T | 1 | a0001c0017 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.3126C>T | p.Asp1042Asp | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/39 | 3698/9350 | 3126/5487 | 1042/1828 | chr15 | 92984389 | |||
| chr15:92985575 | G | A | 1 | a0001c0015 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.3315G>A | p.Thr1105Thr | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/39 | 3887/9350 | 3315/5487 | 1105/1828 | chr15 | 92985575 | |||
| chr15:92985581 | C | T | 1 | a0001c0012 | 2 | HG02280.hp1 HG02922.hp2 |
synonymous_variant | LOW | c.3321C>T | p.Asp1107Asp | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/39 | 3893/9350 | 3321/5487 | 1107/1828 | chr15 | 92985581 | |||
| chr15:92992943 | C | T | 2 | a0001c0009 a0001c0016 |
4 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(1): Show |
synonymous_variant | LOW | c.3540C>T | p.Ser1180Ser | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/39 | 4112/9350 | 3540/5487 | 1180/1828 | chr15 | 92992943 | |||
| chr15:92992967 | C | T | 4 | a0001c0002 a0001c0004 a0001c0013 others(1): Show |
67 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(64): Show |
synonymous_variant | LOW | c.3564C>T | p.Tyr1188Tyr | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/39 | 4136/9350 | 3564/5487 | 1188/1828 | chr15 | 92992967 | |||
| chr15:93009258 | C | T | 1 | a0001c0008 | 2 | HG00323.hp2 HG02486.hp1 |
synonymous_variant | LOW | c.4527C>T | p.Ile1509Ile | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/39 | 5099/9350 | 4527/5487 | 1509/1828 | chr15 | 93009258 | |||
| chr15:93020154 | C | T | 1 | a0001c0016 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.5049C>T | p.Ala1683Ala | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/39 | 5621/9350 | 5049/5487 | 1683/1828 | chr15 | 93020154 | |||
| chr15:93024634 | A | C | 3 | a0001c0004 a0001c0005 a0001c0006 |
35 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(32): Show |
synonymous_variant | LOW | c.5416A>C | p.Arg1806Arg | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 5988/9350 | 5416/5487 | 1806/1828 | chr15 | 93024634 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:93024778 | G | A | 2 | a0001c0001t0011 a0001c0002t0011 |
5 | HG01074.hp1 HG01175.hp1 NA18993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*73G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 73 | chr15 | 93024778 | ||||||
| chr15:93024787 | G | A | 1 | a0001c0003t0014 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*82G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 82 | chr15 | 93024787 | ||||||
| chr15:93024852 | G | T | 1 | a0001c0001t0025 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*147G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 147 | chr15 | 93024852 | ||||||
| chr15:93025065 | G | A | 6 | a0001c0001t0005 a0001c0002t0005 a0001c0003t0005 others(3): Show |
15 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*360G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 360 | chr15 | 93025065 | ||||||
| chr15:93025197 | G | A | 1 | a0001c0001t0006 | 14 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*492G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 492 | chr15 | 93025197 | ||||||
| chr15:93025236 | A | AGGG | 28 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(25): Show |
196 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*533_*535dupGGG | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 536 | INFO_REALIGN_3_PRIME | chr15 | 93025236 | |||||
| chr15:93025595 | C | T | 1 | a0001c0004t0018 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*890C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 890 | chr15 | 93025595 | ||||||
| chr15:93025654 | A | C | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0020 others(17): Show |
178 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*949A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 949 | chr15 | 93025654 | ||||||
| chr15:93025709 | G | A | 1 | a0001c0005t0015 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1004G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1004 | chr15 | 93025709 | ||||||
| chr15:93025852 | ACAT | A | 4 | a0001c0004t0004 a0001c0005t0004 a0001c0005t0015 others(1): Show |
18 | HG00140.hp2 HG00738.hp2 HG01069.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1151_*1153delCAT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1151 | INFO_REALIGN_3_PRIME | chr15 | 93025852 | |||||
| chr15:93026295 | C | T | 1 | a0001c0001t0024 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1590C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1590 | chr15 | 93026295 | ||||||
| chr15:93026317 | C | T | 1 | a0001c0001t0023 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1612C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1612 | chr15 | 93026317 | ||||||
| chr15:93026509 | G | A | 1 | a0001c0004t0010 | 6 | NA18612.hp2 NA18952.hp1 NA18956.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1804G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1804 | chr15 | 93026509 | ||||||
| chr15:93026608 | C | T | 1 | a0001c0013t0019 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1903C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1903 | chr15 | 93026608 | ||||||
| chr15:93026613 | C | G | 1 | a0001c0004t0017 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1908C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1908 | chr15 | 93026613 | ||||||
| chr15:93026624 | G | A | 4 | a0001c0001t0008 a0001c0002t0008 a0001c0003t0008 others(1): Show |
9 | HG00741.hp1 HG01070.hp2 HG01952.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1919G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1919 | chr15 | 93026624 | ||||||
| chr15:93026665 | T | C | 8 | a0001c0001t0005 a0001c0002t0005 a0001c0003t0005 others(5): Show |
19 | HG01167.hp2 HG01169.hp2 HG01257.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1960T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1960 | chr15 | 93026665 | ||||||
| chr15:93026669 | C | T | 1 | a0001c0007t0013 | 2 | HG01243.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1964C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 1964 | chr15 | 93026669 | ||||||
| chr15:93026822 | C | T | 1 | a0001c0001t0022 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2117C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2117 | chr15 | 93026822 | ||||||
| chr15:93027011 | T | C | 51 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(48): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
3_prime_UTR_variant | MODIFIER | c.*2306T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2306 | chr15 | 93027011 | ||||||
| chr15:93027051 | C | T | 1 | a0001c0004t0018 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2346C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2346 | chr15 | 93027051 | ||||||
| chr15:93027309 | T | A | 1 | a0001c0002t0016 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2604T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2604 | chr15 | 93027309 | ||||||
| chr15:93027362 | G | C | 1 | a0001c0001t0020 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2657G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2657 | chr15 | 93027362 | ||||||
| chr15:93027493 | T | C | 11 | a0001c0001t0001 a0001c0001t0020 a0001c0001t0022 others(8): Show |
158 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*2788T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2788 | chr15 | 93027493 | ||||||
| chr15:93027556 | G | C | 11 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0021 others(8): Show |
26 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2851G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 2851 | chr15 | 93027556 | ||||||
| chr15:93027767 | T | C | 3 | a0001c0001t0011 a0001c0001t0021 a0001c0002t0011 |
6 | HG01074.hp1 HG01175.hp1 HG02027.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3062T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 39/39 | 3062 | chr15 | 93027767 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:92901339 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0002g0008 |
2 | HG02717.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.62+40T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92901339 | |||||||
| chr15:92901795 | A | G | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02258.hp2 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.62+496A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92901795 | |||||||
| chr15:92901973 | CAG | C | 3 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 |
3 | NA18967.hp2 NA18994.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.62+676_62+677delGA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92901973 | ||||||
| chr15:92902553 | G | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0003g0001 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.62+1254G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92902553 | |||||||
| chr15:92902628 | G | T | 26 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(23): Show |
26 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.62+1329G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92902628 | |||||||
| chr15:92903085 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 |
3 | NA18942.hp1 NA18951.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.62+1786T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903085 | |||||||
| chr15:92903239 | C | G | 1 | a0001c0001t0003g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.62+1940C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903239 | |||||||
| chr15:92903242 | C | G | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(135): Show |
141 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.62+1943C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903242 | |||||||
| chr15:92903569 | CTT | C | 26 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(23): Show |
26 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.62+2272_62+2273del others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92903569 | ||||||
| chr15:92903639 | C | T | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(135): Show |
141 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.62+2340C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903639 | |||||||
| chr15:92903747 | A | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(1): Show |
5 | HG01123.hp2 HG02683.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.62+2448A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903747 | |||||||
| chr15:92903815 | A | G | 12 | a0001c0001t0001g0259 a0001c0001t0006g0260 a0001c0001t0006g0261 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+2516A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903815 | |||||||
| chr15:92903836 | C | A | 1 | a0001c0002t0008g0012 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.62+2537C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92903836 | |||||||
| chr15:92904063 | T | C | 26 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(23): Show |
26 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.62+2764T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904063 | |||||||
| chr15:92904085 | C | A | 101 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(98): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.62+2786C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904085 | |||||||
| chr15:92904325 | T | C | 3 | a0001c0002t0002g0156 a0001c0007t0003g0157 a0001c0007t0007g0030 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.62+3026T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904325 | |||||||
| chr15:92904401 | T | G | 139 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(136): Show |
142 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.62+3102T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904401 | |||||||
| chr15:92904403 | G | T | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62+3104G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904403 | |||||||
| chr15:92904444 | A | G | 11 | a0001c0002t0002g0223 a0001c0002t0002g0231 a0001c0002t0002g0232 others(8): Show |
11 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.62+3145A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904444 | |||||||
| chr15:92904508 | T | C | 1 | a0001c0012t0002g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.62+3209T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904508 | |||||||
| chr15:92904512 | G | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 |
3 | HG02083.hp1 NA18965.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.62+3213G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904512 | |||||||
| chr15:92904536 | T | G | 9 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(6): Show |
9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.62+3237T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904536 | |||||||
| chr15:92904547 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.62+3248C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904547 | |||||||
| chr15:92904563 | A | G | 1 | a0001c0004t0004g0297 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.62+3264A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904563 | |||||||
| chr15:92904618 | C | T | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62+3319C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904618 | |||||||
| chr15:92904766 | G | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(22): Show |
26 | HG01069.hp1 HG01070.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.62+3467G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904766 | |||||||
| chr15:92904833 | A | G | 2 | a0001c0005t0004g0153 a0001c0005t0004g0154 |
2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.62+3534A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904833 | |||||||
| chr15:92904992 | G | A | 26 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(23): Show |
26 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.62+3693G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92904992 | |||||||
| chr15:92905575 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(90): Show |
94 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.62+4276T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905575 | |||||||
| chr15:92905597 | T | G | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.62+4298T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905597 | |||||||
| chr15:92905653 | C | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(90): Show |
94 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.62+4354C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905653 | |||||||
| chr15:92905780 | A | G | 2 | a0001c0002t0005g0220 a0001c0003t0002g0221 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.62+4481A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905780 | |||||||
| chr15:92905834 | G | A | 62 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0026 others(59): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.62+4535G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905834 | |||||||
| chr15:92905988 | A | G | 1 | a0001c0003t0003g0152 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.62+4689A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92905988 | |||||||
| chr15:92906030 | A | G | 6 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.62+4731A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906030 | |||||||
| chr15:92906095 | C | T | 3 | a0001c0001t0008g0217 a0001c0001t0008g0218 a0001c0001t0008g0219 |
3 | HG03239.hp2 HG03688.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.62+4796C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906095 | |||||||
| chr15:92906144 | T | A | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(118): Show |
124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.62+4845T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906144 | |||||||
| chr15:92906183 | C | CT | 9 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(6): Show |
9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.62+4891dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906183 | ||||||
| chr15:92906238 | T | C | 2 | a0001c0002t0002g0156 a0001c0007t0003g0157 |
2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.62+4939T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906238 | |||||||
| chr15:92906267 | C | T | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.62+4968C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906267 | |||||||
| chr15:92906359 | G | A | 12 | a0001c0001t0001g0259 a0001c0001t0006g0260 a0001c0001t0006g0261 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+5060G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906359 | |||||||
| chr15:92906411 | A | G | 9 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(6): Show |
9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.62+5112A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906411 | |||||||
| chr15:92906413 | T | C | 1 | a0001c0001t0011g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.62+5114T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906413 | |||||||
| chr15:92906466 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.62+5167C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906466 | |||||||
| chr15:92906521 | A | C | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.62+5222A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906521 | |||||||
| chr15:92906539 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.62+5240C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906539 | |||||||
| chr15:92906559 | C | G | 1 | a0001c0002t0001g0258 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.62+5260C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906559 | |||||||
| chr15:92906629 | T | C | 1 | a0001c0005t0004g0159 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.62+5330T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906629 | |||||||
| chr15:92906662 | A | AT | 8 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(5): Show |
8 | HG00423.hp2 HG02040.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.62+5364dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906662 | ||||||
| chr15:92906662 | A | ATT | 15 | a0001c0001t0006g0253 a0001c0002t0001g0244 a0001c0002t0001g0246 others(12): Show |
15 | HG00558.hp1 HG01943.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.62+5364_62+5365ins others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906662 | ||||||
| chr15:92906664 | C | T | 26 | a0001c0001t0006g0253 a0001c0002t0001g0233 a0001c0002t0001g0234 others(23): Show |
26 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.62+5365C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906664 | |||||||
| chr15:92906664 | CT | C | 8 | a0001c0001t0001g0026 a0001c0001t0001g0259 a0001c0001t0002g0278 others(5): Show |
9 | HG01074.hp2 HG01169.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.62+5385delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906664 | ||||||
| chr15:92906664 | CTT | C | 95 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(92): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.62+5384_62+5385del others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906664 | ||||||
| chr15:92906664 | CTTT | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.62+5383_62+5385del others(3): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92906664 | ||||||
| chr15:92906720 | T | C | 12 | a0001c0001t0001g0259 a0001c0001t0006g0260 a0001c0001t0006g0261 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+5421T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906720 | |||||||
| chr15:92906733 | T | G | 2 | a0001c0005t0004g0153 a0001c0005t0004g0154 |
2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.62+5434T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906733 | |||||||
| chr15:92906739 | A | G | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(118): Show |
124 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.62+5440A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906739 | |||||||
| chr15:92906775 | A | C | 1 | a0001c0001t0008g0219 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.62+5476A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906775 | |||||||
| chr15:92906814 | G | A | 1 | a0001c0004t0007g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.62+5515G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906814 | |||||||
| chr15:92906927 | A | G | 19 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02083.hp1 others(16): Show |
intron_variant | MODIFIER | c.62+5628A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92906927 | |||||||
| chr15:92907002 | A | G | 4 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG00438.hp2 HG02040.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.62+5703A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907002 | |||||||
| chr15:92907038 | G | C | 2 | a0001c0002t0005g0220 a0001c0003t0002g0221 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.62+5739G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907038 | |||||||
| chr15:92907136 | A | T | 62 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0026 others(59): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.62+5837A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907136 | |||||||
| chr15:92907142 | A | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(110): Show |
116 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.62+5843A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907142 | |||||||
| chr15:92907236 | A | G | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.62+5937A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907236 | |||||||
| chr15:92907754 | A | G | 3 | a0001c0007t0007g0030 a0001c0007t0013g0150 a0001c0007t0013g0151 |
3 | HG01243.hp2 HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.62+6455A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907754 | |||||||
| chr15:92907807 | A | T | 1 | a0001c0003t0003g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.62+6508A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92907807 | |||||||
| chr15:92908003 | A | AT | 119 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(116): Show |
121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.62+6728dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92908003 | ||||||
| chr15:92908003 | A | ATT | 12 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0041 others(9): Show |
12 | HG00621.hp2 HG01258.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.62+6727_62+6728dup others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92908003 | ||||||
| chr15:92908003 | AT | A | 46 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0178 others(43): Show |
47 | HG00323.hp2 HG00735.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.62+6728delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92908003 | ||||||
| chr15:92908102 | G | C | 1 | a0001c0003t0003g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.62+6803G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908102 | |||||||
| chr15:92908380 | A | G | 1 | a0001c0001t0001g0007 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.62+7081A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908380 | |||||||
| chr15:92908396 | T | A | 12 | a0001c0001t0001g0259 a0001c0001t0006g0260 a0001c0001t0006g0261 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+7097T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908396 | |||||||
| chr15:92908486 | G | A | 12 | a0001c0001t0001g0259 a0001c0001t0006g0260 a0001c0001t0006g0261 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+7187G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908486 | |||||||
| chr15:92908556 | G | C | 6 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0009t0002g0044 others(3): Show |
6 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.62+7257G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908556 | |||||||
| chr15:92908559 | T | C | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62+7260T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908559 | |||||||
| chr15:92908668 | C | T | 17 | a0001c0001t0007g0174 a0001c0003t0002g0162 a0001c0003t0002g0169 others(14): Show |
17 | HG01070.hp1 HG01109.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.62+7369C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908668 | |||||||
| chr15:92908865 | T | G | 1 | a0001c0005t0004g0180 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.62+7566T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908865 | |||||||
| chr15:92908896 | A | T | 2 | a0001c0007t0013g0150 a0001c0007t0013g0151 |
2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.62+7597A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908896 | |||||||
| chr15:92908980 | A | G | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62+7681A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92908980 | |||||||
| chr15:92909035 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.62+7736C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909035 | |||||||
| chr15:92909067 | T | C | 123 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(120): Show |
126 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.62+7768T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909067 | |||||||
| chr15:92909073 | G | GACACACC | 93 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(90): Show |
94 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.62+7777_62+7783dup others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909073 | ||||||
| chr15:92909211 | C | G | 9 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(6): Show |
9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.62+7912C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909211 | |||||||
| chr15:92909410 | C | T | 2 | a0001c0001t0003g0274 a0001c0001t0005g0179 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.62+8111C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909410 | |||||||
| chr15:92909616 | G | A | 269 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(266): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.62+8317G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909616 | |||||||
| chr15:92909630 | A | G | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.62+8331A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909630 | |||||||
| chr15:92909803 | C | T | 4 | a0001c0002t0002g0223 a0001c0002t0002g0232 a0001c0002t0005g0224 others(1): Show |
4 | HG02572.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+8504C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909803 | |||||||
| chr15:92909813 | G | A | 12 | a0001c0001t0001g0259 a0001c0001t0006g0260 a0001c0001t0006g0261 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+8514G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909813 | |||||||
| chr15:92909850 | A | G | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.62+8551A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92909850 | |||||||
| chr15:92909939 | C | CGT | 11 | a0001c0001t0001g0259 a0001c0001t0002g0278 a0001c0001t0002g0295 others(8): Show |
11 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.62+8669_62+8670dup others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | ||||||
| chr15:92909939 | C | CGTGT | 7 | a0001c0001t0006g0268 a0001c0001t0006g0269 a0001c0002t0002g0045 others(4): Show |
7 | HG00642.hp1 HG02148.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.62+8667_62+8670dup others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | ||||||
| chr15:92909939 | C | CGTGTGT | 24 | a0001c0001t0006g0253 a0001c0002t0001g0233 a0001c0002t0001g0234 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.62+8665_62+8670dup others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | ||||||
| chr15:92909939 | C | CGTGTGTG others(1): Show |
3 | a0001c0002t0001g0242 a0001c0002t0001g0255 a0001c0005t0004g0153 |
3 | NA18959.hp2 NA19081.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.62+8663_62+8670dup others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | ||||||
| chr15:92909939 | C | CGTGTGTG others(3): Show |
1 | a0001c0005t0004g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.62+8661_62+8670dup others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | ||||||
| chr15:92909939 | CGT | C | 3 | a0001c0002t0002g0275 a0001c0002t0016g0280 a0001c0003t0005g0124 |
3 | HG00099.hp2 HG01975.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.62+8669_62+8670del others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | ||||||
| chr15:92909939 | CGTGTGTG others(3): Show |
C | 10 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0098 others(7): Show |
10 | HG01346.hp1 HG01361.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.62+8661_62+8670del others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | ||||||
| chr15:92909939 | CGTGTGTG others(5): Show |
C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(175): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.62+8659_62+8670del others(12): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92909939 | ||||||
| chr15:92910044 | T | C | 36 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(33): Show |
36 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.62+8745T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92910044 | |||||||
| chr15:92910116 | C | T | 25 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(22): Show |
25 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.62+8817C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92910116 | |||||||
| chr15:92910648 | C | T | 1 | a0001c0003t0003g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.62+9349C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92910648 | |||||||
| chr15:92911020 | G | A | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(82): Show |
88 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.62+9721G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911020 | |||||||
| chr15:92911093 | C | A | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.62+9794C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911093 | |||||||
| chr15:92911152 | C | T | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(105): Show |
111 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.62+9853C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911152 | |||||||
| chr15:92911491 | A | C | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.62+10192A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911491 | |||||||
| chr15:92911519 | C | T | 1 | a0001c0004t0018g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62+10220C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911519 | |||||||
| chr15:92911562 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(91): Show |
95 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.62+10263A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911562 | |||||||
| chr15:92911583 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0003g0001 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.62+10284C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911583 | |||||||
| chr15:92911654 | G | A | 1 | a0001c0003t0005g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.62+10355G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911654 | |||||||
| chr15:92911689 | C | T | 2 | a0001c0001t0002g0293 a0001c0001t0002g0294 |
2 | HG00544.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.62+10390C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911689 | |||||||
| chr15:92911692 | A | G | 1 | a0001c0016t0002g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.62+10393A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911692 | |||||||
| chr15:92911801 | C | G | 106 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(103): Show |
109 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.62+10502C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911801 | |||||||
| chr15:92911960 | T | C | 12 | a0001c0001t0001g0259 a0001c0001t0006g0260 a0001c0001t0006g0261 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+10661T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92911960 | |||||||
| chr15:92912012 | A | C | 1 | a0001c0002t0001g0254 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.62+10713A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912012 | |||||||
| chr15:92912147 | G | GT | 12 | a0001c0001t0001g0259 a0001c0001t0006g0260 a0001c0001t0006g0261 others(9): Show |
12 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.62+10857dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92912147 | ||||||
| chr15:92912241 | G | A | 102 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0026 others(99): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.62+10942G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912241 | |||||||
| chr15:92912336 | G | A | 1 | a0001c0001t0006g0261 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.62+11037G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912336 | |||||||
| chr15:92912387 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.62+11088C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912387 | |||||||
| chr15:92912550 | T | C | 3 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0295 |
3 | HG02965.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.62+11251T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912550 | |||||||
| chr15:92912582 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0122 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.62+11283A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912582 | |||||||
| chr15:92912602 | T | C | 1 | a0001c0004t0018g0025 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.62+11303T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912602 | |||||||
| chr15:92912690 | C | T | 9 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(6): Show |
9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.62+11391C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912690 | |||||||
| chr15:92912723 | CA | C | 37 | a0001c0001t0001g0095 a0001c0001t0011g0292 a0001c0001t0025g0104 others(34): Show |
37 | HG00621.hp2 HG00673.hp2 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.62+11425delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912723 | |||||||
| chr15:92912748 | C | A | 3 | a0001c0002t0001g0233 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | NA18950.hp1 NA18973.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.62+11449C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912748 | |||||||
| chr15:92912752 | T | C | 29 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0183 others(26): Show |
29 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.62+11453T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912752 | |||||||
| chr15:92912764 | GACCTCGT others(9): Show |
G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG03492.hp2 HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.62+11470_62+11485d others(18): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92912764 | ||||||
| chr15:92912769 | CGTGATCC others(9): Show |
C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.62+11481_62+11496d others(18): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92912769 | ||||||
| chr15:92912770 | G | A | 1 | a0001c0006t0004g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.62+11471G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912770 | |||||||
| chr15:92912780 | A | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.62+11481A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912780 | |||||||
| chr15:92912781 | A | G | 2 | a0001c0001t0002g0293 a0001c0001t0002g0294 |
2 | HG00544.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.62+11482A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912781 | |||||||
| chr15:92912797 | G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.62+11498G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912797 | |||||||
| chr15:92912802 | G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.62+11503G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912802 | |||||||
| chr15:92912839 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.63-11482T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912839 | |||||||
| chr15:92912912 | C | T | 1 | a0001c0001t0003g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.63-11409C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92912912 | |||||||
| chr15:92913166 | A | G | 1 | a0001c0002t0001g0244 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.63-11155A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913166 | |||||||
| chr15:92913228 | G | A | 3 | a0001c0003t0012g0126 a0001c0003t0012g0131 a0001c0003t0012g0132 |
3 | HG01257.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.63-11093G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913228 | |||||||
| chr15:92913425 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0025g0104 |
2 | HG00621.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.63-10896C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913425 | |||||||
| chr15:92913689 | A | C | 18 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(15): Show |
18 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.63-10632A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913689 | |||||||
| chr15:92913786 | C | T | 6 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-10535C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913786 | |||||||
| chr15:92913813 | C | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.63-10508C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913813 | |||||||
| chr15:92913818 | A | T | 52 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0177 others(49): Show |
54 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.63-10503A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913818 | |||||||
| chr15:92913844 | C | T | 2 | a0001c0002t0005g0220 a0001c0003t0002g0221 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.63-10477C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913844 | |||||||
| chr15:92913910 | T | G | 2 | a0001c0001t0003g0274 a0001c0001t0005g0179 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.63-10411T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92913910 | |||||||
| chr15:92914278 | T | G | 1 | a0001c0006t0005g0133 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.63-10043T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914278 | |||||||
| chr15:92914287 | A | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG00673.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.63-10034A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914287 | |||||||
| chr15:92914420 | T | C | 67 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(64): Show |
70 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.63-9901T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914420 | |||||||
| chr15:92914561 | A | C | 2 | a0001c0002t0009g0022 a0001c0004t0018g0025 |
2 | HG01361.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.63-9760A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914561 | |||||||
| chr15:92914731 | A | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.63-9590A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914731 | |||||||
| chr15:92914923 | T | C | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.63-9398T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92914923 | |||||||
| chr15:92915020 | A | C | 1 | a0001c0003t0003g0147 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.63-9301A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915020 | |||||||
| chr15:92915071 | C | T | 2 | a0001c0001t0003g0274 a0001c0001t0005g0179 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.63-9250C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915071 | |||||||
| chr15:92915124 | T | G | 61 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0026 others(58): Show |
63 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.63-9197T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915124 | |||||||
| chr15:92915279 | G | GT | 16 | a0001c0001t0001g0118 a0001c0001t0001g0259 a0001c0001t0006g0253 others(13): Show |
16 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.63-9029dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92915279 | ||||||
| chr15:92915306 | G | A | 1 | a0001c0005t0007g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63-9015G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915306 | |||||||
| chr15:92915401 | A | T | 2 | a0001c0002t0002g0045 a0001c0002t0002g0046 |
2 | NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.63-8920A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915401 | |||||||
| chr15:92915451 | T | C | 1 | a0001c0003t0001g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.63-8870T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915451 | |||||||
| chr15:92915475 | C | T | 83 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0026 others(80): Show |
86 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.63-8846C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915475 | |||||||
| chr15:92915575 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.63-8746A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915575 | |||||||
| chr15:92915614 | C | G | 4 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0005g0224 others(1): Show |
4 | HG02572.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.63-8707C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915614 | |||||||
| chr15:92915695 | T | C | 6 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-8626T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915695 | |||||||
| chr15:92915882 | G | A | 239 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(236): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.63-8439G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915882 | |||||||
| chr15:92915927 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63-8394C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92915927 | |||||||
| chr15:92916011 | ACTCTCTT | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(105): Show |
111 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.63-8306_63-8300del others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92916011 | ||||||
| chr15:92916102 | C | T | 65 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(62): Show |
68 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.63-8219C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92916102 | |||||||
| chr15:92916223 | C | T | 12 | a0001c0001t0001g0130 a0001c0001t0001g0143 a0001c0003t0001g0134 others(9): Show |
13 | HG00323.hp2 HG00741.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.63-8098C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92916223 | |||||||
| chr15:92916236 | T | TA | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0016 others(107): Show |
113 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.63-8084dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92916236 | ||||||
| chr15:92916490 | C | T | 2 | a0001c0002t0002g0275 a0001c0002t0016g0280 |
2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.63-7831C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92916490 | |||||||
| chr15:92916519 | C | T | 1 | a0001c0004t0004g0092 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.63-7802C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92916519 | |||||||
| chr15:92916565 | T | G | 3 | a0001c0003t0003g0161 a0001c0003t0005g0160 a0001c0007t0003g0157 |
3 | HG01884.hp1 HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.63-7756T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92916565 | |||||||
| chr15:92917025 | G | A | 15 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(12): Show |
16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.63-7296G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917025 | |||||||
| chr15:92917033 | G | C | 2 | a0001c0007t0013g0150 a0001c0007t0013g0151 |
2 | HG01243.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.63-7288G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917033 | |||||||
| chr15:92917160 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.63-7161A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917160 | |||||||
| chr15:92917219 | C | T | 1 | a0001c0003t0005g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.63-7102C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917219 | |||||||
| chr15:92917375 | A | G | 6 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0002g0232 others(3): Show |
6 | HG02572.hp2 HG02970.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.63-6946A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917375 | |||||||
| chr15:92917403 | A | G | 6 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-6918A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917403 | |||||||
| chr15:92917461 | T | C | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02258.hp2 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.63-6860T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917461 | |||||||
| chr15:92917475 | C | T | 2 | a0001c0001t0003g0274 a0001c0001t0005g0179 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.63-6846C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917475 | |||||||
| chr15:92917510 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.63-6811G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917510 | |||||||
| chr15:92917547 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.63-6774C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917547 | |||||||
| chr15:92917605 | T | C | 2 | a0001c0002t0002g0275 a0001c0002t0016g0280 |
2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.63-6716T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917605 | |||||||
| chr15:92917614 | C | T | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
4 | HG02080.hp2 NA18953.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-6707C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917614 | |||||||
| chr15:92917761 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.63-6560A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92917761 | |||||||
| chr15:92918015 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.63-6306G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918015 | |||||||
| chr15:92918033 | C | G | 239 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(236): Show |
243 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(240): Show |
intron_variant | MODIFIER | c.63-6288C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918033 | |||||||
| chr15:92918141 | C | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.63-6180C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918141 | |||||||
| chr15:92918266 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.63-6055T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918266 | |||||||
| chr15:92918301 | A | G | 24 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(21): Show |
24 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.63-6020A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918301 | |||||||
| chr15:92918347 | G | GT | 6 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0002g0232 others(3): Show |
6 | HG02572.hp2 HG02970.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.63-5967dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92918347 | ||||||
| chr15:92918562 | T | G | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.63-5759T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918562 | |||||||
| chr15:92918582 | C | G | 8 | a0001c0003t0003g0161 a0001c0003t0003g0164 a0001c0003t0003g0167 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.63-5739C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918582 | |||||||
| chr15:92918737 | TGTC | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
5 | HG01346.hp1 HG01361.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.63-5581_63-5579del others(3): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92918737 | ||||||
| chr15:92918806 | C | T | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63-5515C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918806 | |||||||
| chr15:92918820 | T | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.63-5501T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92918820 | |||||||
| chr15:92918856 | CATATAT | C | 6 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-5456_63-5451del others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92918856 | ||||||
| chr15:92919029 | T | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0023g0052 |
3 | HG00544.hp2 NA18612.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.63-5292T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919029 | |||||||
| chr15:92919056 | G | A | 2 | a0001c0002t0005g0220 a0001c0003t0002g0221 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.63-5265G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919056 | |||||||
| chr15:92919112 | T | C | 1 | a0001c0003t0005g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.63-5209T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919112 | |||||||
| chr15:92919136 | T | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.63-5185T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919136 | |||||||
| chr15:92919307 | CT | C | 41 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0235 others(38): Show |
41 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.63-5004delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92919307 | ||||||
| chr15:92919374 | G | C | 1 | a0001c0003t0003g0290 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.63-4947G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919374 | |||||||
| chr15:92919579 | A | G | 3 | a0001c0001t0001g0095 a0001c0001t0025g0104 a0001c0002t0001g0091 |
3 | HG00621.hp2 HG03834.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.63-4742A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919579 | |||||||
| chr15:92919705 | A | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.63-4616A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919705 | |||||||
| chr15:92919730 | G | T | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.63-4591G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919730 | |||||||
| chr15:92919778 | C | G | 1 | a0001c0001t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.63-4543C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919778 | |||||||
| chr15:92919843 | A | G | 2 | a0001c0002t0005g0220 a0001c0003t0002g0221 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.63-4478A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92919843 | |||||||
| chr15:92920042 | C | A | 15 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(12): Show |
16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.63-4279C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920042 | |||||||
| chr15:92920050 | C | A | 1 | a0001c0004t0010g0105 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.63-4271C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920050 | |||||||
| chr15:92920129 | T | C | 3 | a0001c0002t0002g0156 a0001c0007t0003g0157 a0001c0007t0007g0030 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.63-4192T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920129 | |||||||
| chr15:92920145 | G | A | 8 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0005g0220 others(5): Show |
8 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.63-4176G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920145 | |||||||
| chr15:92920146 | CT | C | 42 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(39): Show |
42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.63-4165delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92920146 | ||||||
| chr15:92920247 | G | A | 11 | a0001c0002t0001g0286 a0001c0002t0002g0156 a0001c0002t0002g0275 others(8): Show |
11 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.63-4074G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920247 | |||||||
| chr15:92920278 | A | G | 8 | a0001c0002t0001g0286 a0001c0002t0002g0275 a0001c0002t0005g0277 others(5): Show |
8 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.63-4043A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920278 | |||||||
| chr15:92920344 | T | C | 13 | a0001c0001t0001g0016 a0001c0002t0001g0234 a0001c0002t0008g0012 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.63-3977T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920344 | |||||||
| chr15:92920350 | A | C | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.63-3971A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920350 | |||||||
| chr15:92920383 | G | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.63-3938G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920383 | |||||||
| chr15:92920401 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.63-3920T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920401 | |||||||
| chr15:92920472 | C | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0177 others(43): Show |
48 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.63-3849C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920472 | |||||||
| chr15:92920592 | C | CT | 3 | a0001c0007t0007g0030 a0001c0007t0013g0150 a0001c0007t0013g0151 |
3 | HG01243.hp2 HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.63-3725dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92920592 | ||||||
| chr15:92920625 | G | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
5 | HG01346.hp1 HG01361.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.63-3696G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920625 | |||||||
| chr15:92920644 | A | C | 1 | a0001c0016t0002g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.63-3677A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920644 | |||||||
| chr15:92920677 | T | C | 3 | a0001c0002t0002g0156 a0001c0007t0003g0157 a0001c0007t0007g0030 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.63-3644T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920677 | |||||||
| chr15:92920930 | A | T | 2 | a0001c0005t0004g0153 a0001c0005t0004g0154 |
2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.63-3391A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92920930 | |||||||
| chr15:92921146 | A | G | 42 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(39): Show |
42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.63-3175A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921146 | |||||||
| chr15:92921155 | A | C | 1 | a0001c0001t0001g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.63-3166A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921155 | |||||||
| chr15:92921236 | T | C | 6 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0058 others(3): Show |
6 | HG01109.hp1 HG02280.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-3085T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921236 | |||||||
| chr15:92921239 | G | A | 1 | a0001c0005t0004g0287 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.63-3082G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921239 | |||||||
| chr15:92921279 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.63-3042A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921279 | |||||||
| chr15:92921384 | G | C | 1 | a0001c0003t0005g0124 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.63-2937G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921384 | |||||||
| chr15:92921398 | C | T | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.63-2923C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921398 | |||||||
| chr15:92921632 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.63-2689A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921632 | |||||||
| chr15:92921695 | T | C | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.63-2626T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921695 | |||||||
| chr15:92921701 | G | A | 1 | a0001c0001t0006g0270 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.63-2620G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921701 | |||||||
| chr15:92921776 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.63-2545C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921776 | |||||||
| chr15:92921821 | C | T | 1 | a0001c0003t0003g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.63-2500C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921821 | |||||||
| chr15:92921954 | A | G | 1 | a0001c0002t0005g0220 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.63-2367A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921954 | |||||||
| chr15:92921957 | G | A | 251 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.63-2364G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92921957 | |||||||
| chr15:92922162 | G | T | 2 | a0001c0002t0001g0233 a0001c0002t0001g0238 |
2 | NA18973.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.63-2159G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922162 | |||||||
| chr15:92922199 | G | A | 1 | a0001c0003t0003g0003 | 2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.63-2122G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922199 | |||||||
| chr15:92922314 | G | A | 6 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0228 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.63-2007G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922314 | |||||||
| chr15:92922466 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0025g0104 |
2 | HG00621.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.63-1855T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922466 | |||||||
| chr15:92922475 | G | A | 1 | a0001c0003t0005g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63-1846G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922475 | |||||||
| chr15:92922697 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.63-1624C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922697 | |||||||
| chr15:92922772 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02523.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.63-1549C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92922772 | |||||||
| chr15:92923039 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.63-1282C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923039 | |||||||
| chr15:92923078 | T | C | 1 | a0001c0001t0011g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.63-1243T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923078 | |||||||
| chr15:92923143 | T | C | 2 | a0001c0002t0011g0256 a0001c0002t0011g0257 |
2 | NA19000.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.63-1178T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923143 | |||||||
| chr15:92923167 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.63-1154C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923167 | |||||||
| chr15:92923304 | A | C | 2 | a0001c0001t0002g0278 a0001c0001t0002g0295 |
2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.63-1017A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923304 | |||||||
| chr15:92923385 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.63-936C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923385 | |||||||
| chr15:92923392 | C | CTG | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.63-928_63-927dupTG | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92923392 | ||||||
| chr15:92923413 | A | G | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.63-908A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923413 | |||||||
| chr15:92923561 | G | GT | 26 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0117 others(23): Show |
26 | HG00140.hp1 HG00438.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.63-740dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92923561 | ||||||
| chr15:92923561 | GT | G | 26 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(23): Show |
27 | HG00735.hp2 HG01069.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.63-740delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | INFO_REALIGN_3_PRIME | chr15 | 92923561 | ||||||
| chr15:92923569 | T | TG | 5 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0005g0224 others(2): Show |
5 | HG02572.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.63-752_63-751insG | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923569 | |||||||
| chr15:92923668 | C | T | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.63-653C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923668 | |||||||
| chr15:92923800 | G | A | 1 | a0001c0003t0008g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.63-521G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923800 | |||||||
| chr15:92923927 | A | G | 6 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0002g0232 others(3): Show |
6 | HG02572.hp2 HG02970.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.63-394A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92923927 | |||||||
| chr15:92924124 | G | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(186): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.63-197G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92924124 | |||||||
| chr15:92924161 | C | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.63-160C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92924161 | |||||||
| chr15:92924212 | T | C | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.63-109T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 2/38 | chr15 | 92924212 | |||||||
| chr15:92924664 | T | A | 23 | a0001c0001t0007g0174 a0001c0002t0002g0231 a0001c0002t0003g0227 others(20): Show |
23 | HG01070.hp1 HG01109.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.294+112T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92924664 | |||||||
| chr15:92924846 | T | A | 3 | a0001c0002t0002g0156 a0001c0007t0003g0157 a0001c0007t0007g0030 |
3 | HG02630.hp1 HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.294+294T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92924846 | |||||||
| chr15:92924854 | G | A | 2 | a0001c0002t0011g0256 a0001c0002t0011g0257 |
2 | NA19000.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.294+302G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92924854 | |||||||
| chr15:92924863 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.294+311C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92924863 | |||||||
| chr15:92924913 | G | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG00438.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.294+361G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92924913 | |||||||
| chr15:92925045 | C | G | 1 | a0001c0002t0001g0241 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.294+493C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925045 | |||||||
| chr15:92925046 | C | G | 199 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.294+494C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925046 | |||||||
| chr15:92925297 | C | T | 2 | a0001c0002t0005g0220 a0001c0003t0002g0221 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.294+745C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925297 | |||||||
| chr15:92925320 | A | G | 42 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(39): Show |
42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.294+768A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925320 | |||||||
| chr15:92925491 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.294+939T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925491 | |||||||
| chr15:92925539 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.294+987C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925539 | |||||||
| chr15:92925645 | G | A | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.294+1093G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925645 | |||||||
| chr15:92925838 | T | C | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.294+1286T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925838 | |||||||
| chr15:92925965 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.295-1279T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92925965 | |||||||
| chr15:92926119 | G | A | 4 | a0001c0001t0001g0143 a0001c0003t0001g0141 a0001c0003t0003g0128 others(1): Show |
4 | HG01346.hp2 HG02683.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-1125G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926119 | |||||||
| chr15:92926209 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.295-1035G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926209 | |||||||
| chr15:92926212 | A | T | 1 | a0001c0001t0001g0200 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.295-1032A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926212 | |||||||
| chr15:92926258 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.295-986C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926258 | |||||||
| chr15:92926304 | T | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0184 |
2 | HG01167.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.295-940T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926304 | |||||||
| chr15:92926366 | T | C | 1 | a0001c0002t0002g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.295-878T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926366 | |||||||
| chr15:92926630 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.295-614A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926630 | |||||||
| chr15:92926702 | G | T | 41 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0235 others(38): Show |
41 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.295-542G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926702 | |||||||
| chr15:92926766 | G | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.295-478G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926766 | |||||||
| chr15:92926871 | G | A | 2 | a0001c0001t0003g0274 a0001c0001t0005g0179 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.295-373G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92926871 | |||||||
| chr15:92926987 | G | GTATGTT | 267 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(264): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.295-254_295-253ins others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | INFO_REALIGN_3_PRIME | chr15 | 92926987 | ||||||
| chr15:92927090 | A | T | 15 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.295-154A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92927090 | |||||||
| chr15:92927149 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.295-95T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 3/38 | chr15 | 92927149 | |||||||
| chr15:92927762 | T | C | 1 | a0001c0001t0022g0097 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.381+432T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92927762 | |||||||
| chr15:92927830 | A | T | 1 | a0001c0001t0001g0114 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.381+500A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92927830 | |||||||
| chr15:92927841 | C | T | 4 | a0001c0001t0001g0200 a0001c0001t0008g0217 a0001c0001t0008g0218 others(1): Show |
4 | HG03239.hp2 HG03688.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+511C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92927841 | |||||||
| chr15:92927905 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.381+575A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92927905 | |||||||
| chr15:92927986 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.381+656G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92927986 | |||||||
| chr15:92928200 | T | C | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.382-830T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92928200 | |||||||
| chr15:92928233 | C | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.382-797C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92928233 | |||||||
| chr15:92928496 | C | CATTT | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.382-534_382-533ins others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92928496 | |||||||
| chr15:92928691 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(12): Show |
16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.382-339C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92928691 | |||||||
| chr15:92928726 | T | C | 18 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(15): Show |
18 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.382-304T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 4/38 | chr15 | 92928726 | |||||||
| chr15:92929219 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.443+128T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929219 | |||||||
| chr15:92929260 | A | G | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.443+169A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929260 | |||||||
| chr15:92929308 | G | A | 5 | a0001c0002t0002g0156 a0001c0002t0002g0181 a0001c0002t0002g0223 others(2): Show |
5 | HG02572.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+217G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929308 | |||||||
| chr15:92929332 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.443+241T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929332 | |||||||
| chr15:92929352 | C | T | 12 | a0001c0002t0001g0234 a0001c0002t0008g0012 a0001c0002t0008g0015 others(9): Show |
12 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.443+261C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929352 | |||||||
| chr15:92929398 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.443+307T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929398 | |||||||
| chr15:92929416 | G | C | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.443+325G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929416 | |||||||
| chr15:92929459 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+368A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929459 | |||||||
| chr15:92929656 | A | AT | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+568dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92929656 | ||||||
| chr15:92929733 | A | G | 5 | a0001c0004t0010g0105 a0001c0004t0010g0106 a0001c0004t0010g0107 others(2): Show |
5 | NA18612.hp2 NA18952.hp1 NA19083.hp1 others(2): Show |
intron_variant | MODIFIER | c.443+642A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929733 | |||||||
| chr15:92929750 | T | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.443+659T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929750 | |||||||
| chr15:92929866 | T | C | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.443+775T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92929866 | |||||||
| chr15:92930004 | T | A | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.443+913T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930004 | |||||||
| chr15:92930006 | A | T | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.443+915A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930006 | |||||||
| chr15:92930021 | A | AAAGTC | 208 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.443+934_443+935ins others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92930021 | ||||||
| chr15:92930023 | A | AGTCAG | 3 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 |
3 | HG02258.hp2 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.443+934_443+935ins others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92930023 | ||||||
| chr15:92930220 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.443+1129T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930220 | |||||||
| chr15:92930264 | G | A | 2 | a0001c0005t0004g0153 a0001c0005t0004g0154 |
2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.443+1173G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930264 | |||||||
| chr15:92930364 | C | T | 18 | a0001c0001t0007g0174 a0001c0003t0002g0162 a0001c0003t0002g0169 others(15): Show |
18 | HG01070.hp1 HG01109.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.443+1273C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930364 | |||||||
| chr15:92930394 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.443+1303C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930394 | |||||||
| chr15:92930417 | T | C | 3 | a0001c0003t0003g0167 a0001c0003t0003g0171 a0001c0003t0003g0290 |
3 | HG01109.hp2 HG03130.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.443+1326T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930417 | |||||||
| chr15:92930513 | G | A | 1 | a0001c0016t0002g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.443+1422G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930513 | |||||||
| chr15:92930522 | T | C | 212 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.443+1431T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930522 | |||||||
| chr15:92930655 | C | G | 4 | a0001c0009t0002g0044 a0001c0009t0002g0048 a0001c0009t0012g0043 others(1): Show |
4 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.443+1564C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930655 | |||||||
| chr15:92930947 | C | A | 41 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0235 others(38): Show |
41 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.443+1856C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92930947 | |||||||
| chr15:92931268 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.443+2177A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931268 | |||||||
| chr15:92931421 | C | G | 1 | a0001c0002t0001g0237 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.443+2330C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931421 | |||||||
| chr15:92931650 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.443+2559G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931650 | |||||||
| chr15:92931863 | C | CT | 76 | a0001c0001t0001g0016 a0001c0001t0007g0174 a0001c0002t0001g0233 others(73): Show |
76 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.443+2790dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92931863 | ||||||
| chr15:92931887 | G | A | 2 | a0001c0002t0001g0242 a0001c0002t0001g0255 |
2 | NA18959.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.443+2796G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931887 | |||||||
| chr15:92931903 | G | A | 1 | a0001c0003t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.443+2812G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931903 | |||||||
| chr15:92931927 | A | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.443+2836A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931927 | |||||||
| chr15:92931939 | T | C | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.443+2848T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92931939 | |||||||
| chr15:92932008 | G | A | 6 | a0001c0002t0003g0227 a0001c0002t0005g0220 a0001c0002t0005g0228 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.443+2917G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932008 | |||||||
| chr15:92932011 | C | T | 1 | a0001c0005t0004g0159 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.443+2920C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932011 | |||||||
| chr15:92932289 | C | CT | 50 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(47): Show |
50 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.443+3213dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92932289 | ||||||
| chr15:92932324 | G | A | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.443+3233G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932324 | |||||||
| chr15:92932328 | G | A | 247 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(244): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.443+3237G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932328 | |||||||
| chr15:92932400 | G | A | 12 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(9): Show |
12 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.443+3309G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932400 | |||||||
| chr15:92932418 | A | G | 1 | a0001c0003t0003g0149 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.443+3327A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932418 | |||||||
| chr15:92932443 | TC | T | 297 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(294): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.443+3359delC | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92932443 | ||||||
| chr15:92932728 | G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.443+3637G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932728 | |||||||
| chr15:92932760 | T | G | 18 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(15): Show |
18 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.443+3669T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932760 | |||||||
| chr15:92932835 | G | GCAACCTC others(8): Show |
249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.443+3744_443+3745i others(17): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932835 | |||||||
| chr15:92932836 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443+3745T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932836 | |||||||
| chr15:92932836 | T | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.443+3745T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932836 | |||||||
| chr15:92932837 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443+3746G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932837 | |||||||
| chr15:92932838 | A | ACCTCCGC others(3): Show |
1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443+3748_443+3749i others(12): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92932838 | ||||||
| chr15:92932841 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443+3750C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932841 | |||||||
| chr15:92932842 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.443+3751A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932842 | |||||||
| chr15:92932971 | G | T | 1 | a0001c0002t0001g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.443+3880G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932971 | |||||||
| chr15:92932996 | G | A | 1 | a0001c0002t0001g0252 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.443+3905G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92932996 | |||||||
| chr15:92933039 | GC | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(278): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.443+3952delC | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92933039 | ||||||
| chr15:92933042 | CCT | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0099 a0001c0001t0001g0186 |
3 | HG00423.hp1 HG01515.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.443+3952_443+3953d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933042 | |||||||
| chr15:92933043 | C | T | 13 | a0001c0001t0001g0062 a0001c0001t0001g0281 a0001c0002t0001g0286 others(10): Show |
13 | HG00642.hp1 HG00673.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+3952C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933043 | |||||||
| chr15:92933070 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.443+3979A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933070 | |||||||
| chr15:92933120 | A | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.443+4029A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933120 | |||||||
| chr15:92933548 | A | T | 1 | a0001c0002t0005g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.444-3970A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933548 | |||||||
| chr15:92933751 | G | A | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.444-3767G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92933751 | |||||||
| chr15:92934017 | G | A | 13 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(10): Show |
13 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-3501G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92934017 | |||||||
| chr15:92934073 | TC | T | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-3443delC | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92934073 | ||||||
| chr15:92934184 | T | C | 1 | a0001c0003t0002g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.444-3334T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92934184 | |||||||
| chr15:92934424 | AGG | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.444-3089_444-3088d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92934424 | ||||||
| chr15:92934505 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.444-3013C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92934505 | |||||||
| chr15:92934595 | T | C | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.444-2923T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92934595 | |||||||
| chr15:92934745 | C | T | 3 | a0001c0003t0012g0126 a0001c0003t0012g0131 a0001c0003t0012g0132 |
3 | HG01257.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.444-2773C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92934745 | |||||||
| chr15:92935015 | G | GT | 5 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(2): Show |
6 | HG01243.hp1 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.444-2493dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92935015 | ||||||
| chr15:92935038 | C | CT | 63 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0199 others(60): Show |
63 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.444-2466dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92935038 | ||||||
| chr15:92935176 | C | T | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.444-2342C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935176 | |||||||
| chr15:92935196 | T | C | 24 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(21): Show |
24 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.444-2322T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935196 | |||||||
| chr15:92935224 | T | G | 1 | a0001c0003t0001g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.444-2294T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935224 | |||||||
| chr15:92935257 | C | G | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.444-2261C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935257 | |||||||
| chr15:92935282 | C | T | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.444-2236C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935282 | |||||||
| chr15:92935287 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.444-2231C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935287 | |||||||
| chr15:92935331 | C | T | 1 | a0001c0002t0001g0233 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.444-2187C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935331 | |||||||
| chr15:92935333 | A | G | 240 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(237): Show |
245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.444-2185A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935333 | |||||||
| chr15:92935386 | A | C | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.444-2132A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935386 | |||||||
| chr15:92935932 | A | AT | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01175.hp1 HG02083.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.444-1573dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92935932 | ||||||
| chr15:92935982 | G | A | 1 | a0001c0004t0010g0106 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.444-1536G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92935982 | |||||||
| chr15:92936061 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.444-1457C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936061 | |||||||
| chr15:92936110 | C | A | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.444-1408C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936110 | |||||||
| chr15:92936115 | G | A | 1 | a0001c0002t0001g0246 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.444-1403G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936115 | |||||||
| chr15:92936147 | A | G | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.444-1371A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936147 | |||||||
| chr15:92936211 | C | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.444-1307C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936211 | |||||||
| chr15:92936230 | A | G | 1 | a0001c0007t0003g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.444-1288A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936230 | |||||||
| chr15:92936282 | C | T | 3 | a0001c0002t0008g0015 a0001c0004t0007g0020 a0001c0004t0017g0019 |
3 | HG01070.hp2 HG01123.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.444-1236C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936282 | |||||||
| chr15:92936406 | A | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.444-1112A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936406 | |||||||
| chr15:92936432 | C | T | 1 | a0001c0002t0001g0234 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.444-1086C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936432 | |||||||
| chr15:92936568 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.444-950T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936568 | |||||||
| chr15:92936702 | G | T | 1 | a0001c0001t0006g0267 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.444-816G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936702 | |||||||
| chr15:92936725 | G | A | 1 | a0001c0009t0002g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.444-793G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936725 | |||||||
| chr15:92936824 | A | C | 1 | a0001c0001t0008g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.444-694A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936824 | |||||||
| chr15:92936890 | C | T | 1 | a0001c0002t0001g0233 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.444-628C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936890 | |||||||
| chr15:92936975 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.444-543C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92936975 | |||||||
| chr15:92937139 | A | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.444-379A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92937139 | |||||||
| chr15:92937168 | A | G | 1 | a0001c0003t0003g0003 | 2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.444-350A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92937168 | |||||||
| chr15:92937233 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
6 | HG01069.hp1 HG01123.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.444-285G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92937233 | |||||||
| chr15:92937275 | G | GA | 175 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.444-237dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | INFO_REALIGN_3_PRIME | chr15 | 92937275 | ||||||
| chr15:92937365 | T | C | 1 | a0001c0004t0007g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.444-153T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 5/38 | chr15 | 92937365 | |||||||
| chr15:92937638 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.551+13C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92937638 | |||||||
| chr15:92937777 | A | G | 18 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(15): Show |
18 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.551+152A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92937777 | |||||||
| chr15:92937806 | G | A | 4 | a0001c0001t0001g0026 a0001c0001t0003g0001 a0001c0011t0001g0023 others(1): Show |
5 | HG00639.hp2 HG00738.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.551+181G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92937806 | |||||||
| chr15:92937817 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.551+192A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92937817 | |||||||
| chr15:92938116 | A | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.551+491A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938116 | |||||||
| chr15:92938226 | A | G | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.551+601A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938226 | |||||||
| chr15:92938310 | A | G | 6 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0223 others(3): Show |
6 | HG02572.hp2 HG03209.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.551+685A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938310 | |||||||
| chr15:92938441 | C | T | 42 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(39): Show |
42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.551+816C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938441 | |||||||
| chr15:92938666 | G | T | 1 | a0001c0004t0010g0245 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.552-912G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938666 | |||||||
| chr15:92938770 | T | G | 25 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(22): Show |
26 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.552-808T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938770 | |||||||
| chr15:92938996 | C | G | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.552-582C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92938996 | |||||||
| chr15:92939047 | C | CT | 153 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(150): Show |
156 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.552-520dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 92939047 | ||||||
| chr15:92939047 | C | CTT | 6 | a0001c0001t0001g0042 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
6 | HG01346.hp1 HG01361.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.552-521_552-520dup others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 92939047 | ||||||
| chr15:92939047 | CT | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.552-520delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | INFO_REALIGN_3_PRIME | chr15 | 92939047 | ||||||
| chr15:92939337 | C | T | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.552-241C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92939337 | |||||||
| chr15:92939386 | C | T | 5 | a0001c0003t0002g0221 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.552-192C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92939386 | |||||||
| chr15:92939426 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
165 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.552-152G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92939426 | |||||||
| chr15:92939554 | C | T | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.552-24C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 6/38 | chr15 | 92939554 | |||||||
| chr15:92939834 | C | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.692+116C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92939834 | |||||||
| chr15:92939844 | T | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.692+126T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92939844 | |||||||
| chr15:92939872 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.692+154A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92939872 | |||||||
| chr15:92939879 | G | A | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.692+161G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92939879 | |||||||
| chr15:92939946 | A | T | 7 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0156 others(4): Show |
7 | HG02572.hp2 HG02976.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.692+228A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92939946 | |||||||
| chr15:92940024 | A | G | 1 | a0001c0009t0002g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.692+306A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940024 | |||||||
| chr15:92940082 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0034 |
2 | NA18965.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.692+364G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940082 | |||||||
| chr15:92940172 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.692+454G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940172 | |||||||
| chr15:92940311 | G | C | 1 | a0001c0002t0002g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.692+593G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940311 | |||||||
| chr15:92940340 | A | G | 4 | a0001c0003t0002g0162 a0001c0003t0002g0169 a0001c0003t0003g0170 others(1): Show |
4 | HG02630.hp2 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.692+622A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940340 | |||||||
| chr15:92940407 | A | G | 1 | a0001c0003t0005g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.692+689A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940407 | |||||||
| chr15:92940595 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+877T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940595 | |||||||
| chr15:92940596 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+878A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940596 | |||||||
| chr15:92940597 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+879T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940597 | |||||||
| chr15:92940601 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+883A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940601 | |||||||
| chr15:92940602 | T | C | 1 | a0001c0002t0001g0248 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+884T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940602 | |||||||
| chr15:92940605 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+887A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940605 | |||||||
| chr15:92940607 | C | T | 1 | a0001c0002t0001g0248 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.692+889C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940607 | |||||||
| chr15:92940772 | TA | T | 6 | a0001c0003t0002g0221 a0001c0009t0002g0044 a0001c0009t0002g0048 others(3): Show |
6 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.693-1044delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940772 | ||||||
| chr15:92940775 | AAAATATA others(10): Show |
A | 4 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 others(1): Show |
4 | NA18963.hp2 NA18967.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.693-1039_693-1023d others(19): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940775 | ||||||
| chr15:92940784 | AAAATATA others(1): Show |
A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(7): Show |
11 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.693-1024_693-1017d others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940784 | ||||||
| chr15:92940823 | ATAT | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.693-995_693-993del others(3): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940823 | ||||||
| chr15:92940839 | A | T | 2 | a0001c0002t0003g0227 a0001c0002t0005g0228 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.693-983A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940839 | |||||||
| chr15:92940843 | TATATATA others(1): Show |
T | 45 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0054 others(42): Show |
47 | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.693-961_693-954del others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940843 | ||||||
| chr15:92940846 | A | G | 2 | a0001c0003t0012g0126 a0001c0003t0012g0132 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.693-976A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940846 | |||||||
| chr15:92940851 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.693-971A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940851 | |||||||
| chr15:92940876 | A | G | 52 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(49): Show |
52 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.693-946A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940876 | |||||||
| chr15:92940889 | TA | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.693-928delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940889 | ||||||
| chr15:92940895 | T | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.693-927T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940895 | |||||||
| chr15:92940903 | AAT | A | 8 | a0001c0001t0001g0143 a0001c0003t0001g0141 a0001c0003t0001g0144 others(5): Show |
8 | HG01346.hp2 HG01952.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.693-909_693-908del others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940903 | ||||||
| chr15:92940913 | T | TAA | 191 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.693-907_693-906dup others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940913 | ||||||
| chr15:92940913 | T | TATAA | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-908_693-907ins others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940913 | ||||||
| chr15:92940921 | CATATAAA others(20): Show |
C | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.693-883_693-857del others(27): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940921 | ||||||
| chr15:92940938 | A | T | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.693-884A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940938 | |||||||
| chr15:92940940 | T | A | 9 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(6): Show |
9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.693-882T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940940 | |||||||
| chr15:92940940 | TATATATA others(7): Show |
T | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.693-874_693-861del others(14): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940940 | ||||||
| chr15:92940946 | TAA | T | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-874_693-873del others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940946 | ||||||
| chr15:92940954 | AATATATA others(23): Show |
A | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.693-852_693-823del others(30): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940954 | ||||||
| chr15:92940958 | TATATAAA others(5): Show |
T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.693-846_693-835del others(12): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940958 | ||||||
| chr15:92940960 | T | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.693-862T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940960 | |||||||
| chr15:92940964 | A | T | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.693-858A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940964 | |||||||
| chr15:92940966 | T | TATTTA | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-854_693-853ins others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940966 | ||||||
| chr15:92940970 | A | T | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.693-852A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940970 | |||||||
| chr15:92940976 | A | T | 8 | a0001c0001t0001g0101 a0001c0002t0002g0231 a0001c0002t0003g0227 others(5): Show |
8 | HG01884.hp2 HG01928.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.693-846A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940976 | |||||||
| chr15:92940986 | TATATATA others(1): Show |
T | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.693-828_693-821del others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92940986 | ||||||
| chr15:92940992 | T | A | 2 | a0001c0002t0001g0248 a0001c0002t0002g0156 |
2 | HG02976.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.693-830T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940992 | |||||||
| chr15:92940994 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.693-828A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940994 | |||||||
| chr15:92940995 | A | T | 1 | a0001c0002t0001g0248 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.693-827A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92940995 | |||||||
| chr15:92941006 | T | A | 8 | a0001c0002t0001g0248 a0001c0002t0002g0231 a0001c0002t0003g0227 others(5): Show |
8 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.693-816T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941006 | |||||||
| chr15:92941007 | A | T | 8 | a0001c0002t0001g0248 a0001c0002t0002g0231 a0001c0002t0003g0227 others(5): Show |
8 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.693-815A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941007 | |||||||
| chr15:92941008 | A | AT | 185 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.693-803dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | INFO_REALIGN_3_PRIME | chr15 | 92941008 | ||||||
| chr15:92941008 | A | T | 8 | a0001c0001t0001g0101 a0001c0002t0002g0231 a0001c0002t0003g0227 others(5): Show |
8 | HG01884.hp2 HG01928.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.693-814A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941008 | |||||||
| chr15:92941181 | C | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.693-641C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941181 | |||||||
| chr15:92941186 | C | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.693-636C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941186 | |||||||
| chr15:92941281 | C | T | 44 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(41): Show |
44 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.693-541C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941281 | |||||||
| chr15:92941460 | T | C | 52 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(49): Show |
52 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.693-362T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941460 | |||||||
| chr15:92941609 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.693-213A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941609 | |||||||
| chr15:92941655 | T | G | 1 | a0001c0007t0003g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.693-167T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941655 | |||||||
| chr15:92941697 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.693-125G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941697 | |||||||
| chr15:92941802 | C | T | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.693-20C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 7/38 | chr15 | 92941802 | |||||||
| chr15:92942070 | T | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG00673.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.826+115T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942070 | |||||||
| chr15:92942111 | A | G | 1 | a0001c0001t0020g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.826+156A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942111 | |||||||
| chr15:92942226 | C | G | 44 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(41): Show |
44 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.826+271C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942226 | |||||||
| chr15:92942405 | CT | C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(12): Show |
16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.827-424delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 92942405 | ||||||
| chr15:92942411 | T | C | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.827-432T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942411 | |||||||
| chr15:92942471 | C | T | 1 | a0001c0003t0003g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.827-372C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942471 | |||||||
| chr15:92942648 | T | TG | 194 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.827-193dupG | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | INFO_REALIGN_3_PRIME | chr15 | 92942648 | ||||||
| chr15:92942697 | G | C | 7 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0156 others(4): Show |
7 | HG02572.hp2 HG02976.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-146G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 8/38 | chr15 | 92942697 | |||||||
| chr15:92943159 | G | A | 1 | a0001c0006t0004g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1052+91G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943159 | |||||||
| chr15:92943173 | G | A | 1 | a0001c0004t0010g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1052+105G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943173 | |||||||
| chr15:92943323 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1052+255T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943323 | |||||||
| chr15:92943343 | A | G | 1 | a0001c0001t0006g0084 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1052+275A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943343 | |||||||
| chr15:92943391 | A | G | 47 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0054 others(44): Show |
49 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1052+323A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943391 | |||||||
| chr15:92943477 | G | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1052+409G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943477 | |||||||
| chr15:92943596 | T | C | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1052+528T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943596 | |||||||
| chr15:92943673 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1052+605G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943673 | |||||||
| chr15:92943905 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1053-510G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92943905 | |||||||
| chr15:92944001 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1053-414G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92944001 | |||||||
| chr15:92944115 | C | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1053-300C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92944115 | |||||||
| chr15:92944156 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1053-259T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92944156 | |||||||
| chr15:92944231 | AGT | A | 4 | a0001c0009t0002g0044 a0001c0009t0002g0048 a0001c0009t0012g0043 others(1): Show |
4 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1053-181_1053-180d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | INFO_REALIGN_3_PRIME | chr15 | 92944231 | ||||||
| chr15:92944268 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0087 |
2 | NA18973.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1053-147C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92944268 | |||||||
| chr15:92944270 | C | G | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1053-145C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 9/38 | chr15 | 92944270 | |||||||
| chr15:92944624 | G | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.1153+109G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92944624 | |||||||
| chr15:92944678 | G | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1153+163G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92944678 | |||||||
| chr15:92944864 | T | TAGTGAAG others(1): Show |
52 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(49): Show |
52 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1153+350_1153+357d others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr15 | 92944864 | ||||||
| chr15:92944884 | G | A | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1153+369G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92944884 | |||||||
| chr15:92944965 | A | G | 8 | a0001c0001t0007g0174 a0001c0002t0002g0045 a0001c0002t0002g0046 others(5): Show |
8 | HG02055.hp1 HG02572.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1153+450A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92944965 | |||||||
| chr15:92945085 | T | A | 160 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(157): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1153+570T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92945085 | |||||||
| chr15:92945174 | C | T | 9 | a0001c0001t0001g0026 a0001c0001t0001g0298 a0001c0001t0001g0299 others(6): Show |
10 | HG00639.hp2 HG00738.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.1154-647C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92945174 | |||||||
| chr15:92945302 | T | C | 6 | a0001c0001t0001g0007 a0001c0003t0002g0221 a0001c0009t0002g0044 others(3): Show |
6 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154-519T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92945302 | |||||||
| chr15:92945389 | C | CT | 48 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0101 others(45): Show |
48 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1154-430dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr15 | 92945389 | ||||||
| chr15:92945392 | C | CTT | 11 | a0001c0001t0006g0253 a0001c0001t0006g0260 a0001c0001t0006g0261 others(8): Show |
11 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.1154-428_1154-427d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr15 | 92945392 | ||||||
| chr15:92945392 | C | T | 223 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1154-429C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92945392 | |||||||
| chr15:92945395 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(292): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1154-426C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | chr15 | 92945395 | |||||||
| chr15:92945696 | AT | A | 10 | a0001c0001t0003g0274 a0001c0001t0005g0179 a0001c0002t0001g0242 others(7): Show |
10 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1154-113delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 10/38 | INFO_REALIGN_3_PRIME | chr15 | 92945696 | ||||||
| chr15:92945946 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0118 |
2 | NA18939.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1198+81A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 11/38 | chr15 | 92945946 | |||||||
| chr15:92946472 | C | CTTTTA | 3 | a0001c0002t0002g0231 a0001c0002t0005g0220 a0001c0002t0005g0229 |
3 | HG02572.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1377+274_1377+278d others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 92946472 | ||||||
| chr15:92946517 | C | T | 13 | a0001c0001t0001g0016 a0001c0002t0001g0234 a0001c0002t0008g0012 others(10): Show |
13 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.1377+301C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92946517 | |||||||
| chr15:92946805 | A | G | 1 | a0001c0003t0003g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1377+589A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92946805 | |||||||
| chr15:92946862 | C | T | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1377+646C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92946862 | |||||||
| chr15:92946926 | G | A | 5 | a0001c0002t0002g0231 a0001c0002t0005g0220 a0001c0002t0005g0229 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+710G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92946926 | |||||||
| chr15:92946931 | C | CT | 9 | a0001c0003t0003g0161 a0001c0003t0003g0167 a0001c0003t0003g0171 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1377+716dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 92946931 | ||||||
| chr15:92946932 | T | TA | 91 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(88): Show |
92 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1377+731dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | INFO_REALIGN_3_PRIME | chr15 | 92946932 | ||||||
| chr15:92946959 | A | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(143): Show |
150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1377+743A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92946959 | |||||||
| chr15:92947014 | G | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1377+798G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947014 | |||||||
| chr15:92947403 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG00673.hp1 HG02155.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.1377+1187A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947403 | |||||||
| chr15:92947426 | G | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(128): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1377+1210G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947426 | |||||||
| chr15:92947526 | C | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(2): Show |
5 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1377+1310C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947526 | |||||||
| chr15:92947588 | G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1378-1364G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947588 | |||||||
| chr15:92947661 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1378-1291C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947661 | |||||||
| chr15:92947787 | A | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(172): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1378-1165A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947787 | |||||||
| chr15:92947812 | G | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1378-1140G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92947812 | |||||||
| chr15:92948081 | A | G | 1 | a0001c0003t0002g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1378-871A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948081 | |||||||
| chr15:92948270 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(126): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1378-682C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948270 | |||||||
| chr15:92948320 | C | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1378-632C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948320 | |||||||
| chr15:92948506 | G | A | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1378-446G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948506 | |||||||
| chr15:92948523 | T | C | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1378-429T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948523 | |||||||
| chr15:92948629 | C | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1378-323C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948629 | |||||||
| chr15:92948829 | A | G | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1378-123A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948829 | |||||||
| chr15:92948856 | T | G | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1378-96T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 12/38 | chr15 | 92948856 | |||||||
| chr15:92949221 | A | G | 1 | a0001c0002t0002g0275 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1502+145A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949221 | |||||||
| chr15:92949222 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1502+146T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949222 | |||||||
| chr15:92949581 | G | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1502+505G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949581 | |||||||
| chr15:92949607 | C | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1502+531C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949607 | |||||||
| chr15:92949862 | G | A | 2 | a0001c0002t0008g0015 a0001c0004t0007g0020 |
2 | HG01070.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1502+786G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949862 | |||||||
| chr15:92949989 | C | T | 4 | a0001c0002t0002g0156 a0001c0002t0002g0223 a0001c0002t0005g0224 others(1): Show |
4 | HG02572.hp2 HG02976.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1502+913C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92949989 | |||||||
| chr15:92950120 | A | G | 8 | a0001c0001t0007g0174 a0001c0002t0002g0045 a0001c0002t0002g0046 others(5): Show |
8 | HG02055.hp1 HG02572.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1502+1044A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950120 | |||||||
| chr15:92950121 | T | C | 20 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(17): Show |
20 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1502+1045T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950121 | |||||||
| chr15:92950209 | C | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1502+1133C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950209 | |||||||
| chr15:92950210 | A | C | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1502+1134A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950210 | |||||||
| chr15:92950401 | T | A | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1502+1325T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950401 | |||||||
| chr15:92950494 | A | T | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1502+1418A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950494 | |||||||
| chr15:92950646 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1502+1570T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950646 | |||||||
| chr15:92950707 | C | T | 1 | a0001c0004t0007g0014 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1502+1631C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950707 | |||||||
| chr15:92950752 | T | TA | 91 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0207 others(88): Show |
91 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1502+1690dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | INFO_REALIGN_3_PRIME | chr15 | 92950752 | ||||||
| chr15:92950796 | T | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1502+1720T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950796 | |||||||
| chr15:92950841 | C | T | 9 | a0001c0002t0001g0286 a0001c0002t0005g0277 a0001c0002t0005g0279 others(6): Show |
9 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1502+1765C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950841 | |||||||
| chr15:92950967 | A | G | 20 | a0001c0001t0001g0281 a0001c0001t0001g0298 a0001c0001t0001g0299 others(17): Show |
20 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1502+1891A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950967 | |||||||
| chr15:92950975 | A | G | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1502+1899A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92950975 | |||||||
| chr15:92951181 | G | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1502+2105G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951181 | |||||||
| chr15:92951458 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1503-1899A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951458 | |||||||
| chr15:92951461 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1503-1896G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951461 | |||||||
| chr15:92951524 | G | A | 1 | a0001c0003t0005g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1503-1833G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951524 | |||||||
| chr15:92951616 | C | T | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1503-1741C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951616 | |||||||
| chr15:92951748 | A | G | 126 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(123): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.1503-1609A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951748 | |||||||
| chr15:92951751 | A | G | 9 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(6): Show |
9 | HG01192.hp1 HG01433.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.1503-1606A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951751 | |||||||
| chr15:92951771 | A | G | 10 | a0001c0002t0001g0286 a0001c0002t0002g0275 a0001c0002t0005g0277 others(7): Show |
10 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1503-1586A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951771 | |||||||
| chr15:92951856 | A | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1503-1501A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951856 | |||||||
| chr15:92951886 | A | C | 1 | a0001c0001t0011g0292 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1503-1471A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92951886 | |||||||
| chr15:92952256 | A | G | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1503-1101A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952256 | |||||||
| chr15:92952389 | C | T | 5 | a0001c0002t0002g0231 a0001c0002t0005g0220 a0001c0002t0005g0229 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1503-968C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952389 | |||||||
| chr15:92952461 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1503-896G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952461 | |||||||
| chr15:92952743 | A | C | 132 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1503-614A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952743 | |||||||
| chr15:92952778 | G | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1503-579G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952778 | |||||||
| chr15:92952836 | G | A | 1 | a0001c0001t0003g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1503-521G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952836 | |||||||
| chr15:92952918 | G | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.1503-439G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92952918 | |||||||
| chr15:92953176 | A | G | 1 | a0001c0001t0006g0084 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1503-181A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 13/38 | chr15 | 92953176 | |||||||
| chr15:92953644 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(234): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1719+71C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953644 | |||||||
| chr15:92953717 | T | C | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1719+144T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953717 | |||||||
| chr15:92953808 | G | A | 42 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(39): Show |
42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1719+235G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953808 | |||||||
| chr15:92953875 | T | C | 5 | a0001c0001t0001g0007 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1719+302T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953875 | |||||||
| chr15:92953880 | A | G | 2 | a0001c0010t0002g0182 a0001c0010t0002g0222 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1719+307A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953880 | |||||||
| chr15:92953948 | T | C | 54 | a0001c0001t0001g0016 a0001c0001t0002g0293 a0001c0001t0002g0294 others(51): Show |
54 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.1719+375T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92953948 | |||||||
| chr15:92954208 | C | G | 13 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0295 others(10): Show |
13 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1719+635C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954208 | |||||||
| chr15:92954250 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(130): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1719+677C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954250 | |||||||
| chr15:92954332 | C | T | 49 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0235 others(46): Show |
49 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.1719+759C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954332 | |||||||
| chr15:92954395 | G | A | 2 | a0001c0001t0003g0274 a0001c0001t0005g0179 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1719+822G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954395 | |||||||
| chr15:92954635 | C | T | 2 | a0001c0002t0002g0275 a0001c0002t0016g0280 |
2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1720-788C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954635 | |||||||
| chr15:92954875 | T | C | 64 | a0001c0001t0001g0016 a0001c0001t0002g0293 a0001c0001t0002g0294 others(61): Show |
64 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.1720-548T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954875 | |||||||
| chr15:92954892 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1720-531A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92954892 | |||||||
| chr15:92955025 | G | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1720-398G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955025 | |||||||
| chr15:92955067 | A | G | 20 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0295 others(17): Show |
20 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1720-356A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955067 | |||||||
| chr15:92955143 | G | C | 2 | a0001c0003t0012g0126 a0001c0003t0012g0132 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1720-280G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955143 | |||||||
| chr15:92955207 | A | G | 1 | a0001c0003t0005g0160 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1720-216A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955207 | |||||||
| chr15:92955312 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1720-111A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955312 | |||||||
| chr15:92955353 | A | G | 9 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0181 others(6): Show |
9 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1720-70A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 14/38 | chr15 | 92955353 | |||||||
| chr15:92955764 | A | G | 1 | a0001c0001t0025g0104 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1809+252A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 15/38 | chr15 | 92955764 | |||||||
| chr15:92956155 | A | G | 251 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1810-304A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 15/38 | chr15 | 92956155 | |||||||
| chr15:92956301 | A | G | 1 | a0001c0003t0003g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1810-158A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 15/38 | chr15 | 92956301 | |||||||
| chr15:92956405 | A | C | 1 | a0001c0006t0004g0163 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1810-54A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 15/38 | chr15 | 92956405 | |||||||
| chr15:92956677 | G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2000+28G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92956677 | |||||||
| chr15:92956850 | G | A | 1 | a0001c0002t0001g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2000+201G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92956850 | |||||||
| chr15:92956950 | A | G | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2000+301A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92956950 | |||||||
| chr15:92956958 | A | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2000+309A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92956958 | |||||||
| chr15:92956993 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(2): Show |
6 | HG01069.hp1 HG01123.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.2000+344G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92956993 | |||||||
| chr15:92957360 | C | T | 2 | a0001c0010t0002g0182 a0001c0010t0002g0222 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2000+711C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957360 | |||||||
| chr15:92957632 | A | G | 13 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(10): Show |
13 | HG00544.hp1 HG00738.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.2000+983A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957632 | |||||||
| chr15:92957738 | T | A | 2 | a0001c0003t0005g0124 a0001c0006t0005g0133 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2000+1089T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957738 | |||||||
| chr15:92957805 | G | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(209): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.2000+1156G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957805 | |||||||
| chr15:92957900 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2000+1251A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957900 | |||||||
| chr15:92957902 | A | G | 2 | a0001c0010t0002g0182 a0001c0010t0002g0222 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2000+1253A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957902 | |||||||
| chr15:92957935 | G | A | 73 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(70): Show |
74 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.2000+1286G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92957935 | |||||||
| chr15:92958031 | G | T | 1 | a0001c0001t0001g0273 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2000+1382G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958031 | |||||||
| chr15:92958041 | G | A | 5 | a0001c0001t0007g0174 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2000+1392G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958041 | |||||||
| chr15:92958168 | T | A | 225 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2000+1519T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958168 | |||||||
| chr15:92958178 | C | G | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2000+1529C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958178 | |||||||
| chr15:92958360 | C | T | 1 | a0001c0002t0001g0241 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2000+1711C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958360 | |||||||
| chr15:92958755 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(130): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.2000+2106C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958755 | |||||||
| chr15:92958782 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2000+2133G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958782 | |||||||
| chr15:92958829 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2000+2180C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958829 | |||||||
| chr15:92958865 | G | A | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2000+2216G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958865 | |||||||
| chr15:92958872 | G | A | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2000+2223G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958872 | |||||||
| chr15:92958889 | T | G | 2 | a0001c0002t0005g0230 a0001c0014t0005g0226 |
2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2000+2240T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92958889 | |||||||
| chr15:92959017 | C | G | 15 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(12): Show |
15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2000+2368C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959017 | |||||||
| chr15:92959082 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2000+2433T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959082 | |||||||
| chr15:92959414 | T | C | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2000+2765T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959414 | |||||||
| chr15:92959711 | C | T | 1 | a0001c0002t0001g0247 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2000+3062C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959711 | |||||||
| chr15:92959832 | T | C | 63 | a0001c0001t0001g0016 a0001c0001t0002g0293 a0001c0001t0002g0294 others(60): Show |
63 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.2000+3183T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959832 | |||||||
| chr15:92959960 | C | T | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2000+3311C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92959960 | |||||||
| chr15:92960160 | A | G | 15 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0259 others(12): Show |
15 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2000+3511A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960160 | |||||||
| chr15:92960163 | G | A | 5 | a0001c0001t0007g0174 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.2000+3514G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960163 | |||||||
| chr15:92960356 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG02523.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2000+3707G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960356 | |||||||
| chr15:92960544 | C | T | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2000+3895C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960544 | |||||||
| chr15:92960580 | T | C | 1 | a0001c0003t0003g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2000+3931T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960580 | |||||||
| chr15:92960597 | T | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.2000+3948T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960597 | |||||||
| chr15:92960686 | A | AT | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2000+4042dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92960686 | ||||||
| chr15:92960686 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.2000+4037A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960686 | |||||||
| chr15:92960705 | G | GT | 47 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0067 others(44): Show |
49 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.2000+4083dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92960705 | ||||||
| chr15:92960705 | G | GTT | 16 | a0001c0001t0001g0200 a0001c0001t0002g0293 a0001c0001t0011g0292 others(13): Show |
16 | HG00544.hp1 HG01175.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.2000+4082_2000+408 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92960705 | ||||||
| chr15:92960705 | G | GTTT | 34 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(31): Show |
35 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.2000+4081_2000+408 others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92960705 | ||||||
| chr15:92960705 | G | GTTTT | 20 | a0001c0001t0001g0016 a0001c0001t0009g0010 a0001c0002t0001g0236 others(17): Show |
20 | HG00423.hp2 HG00639.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.2000+4080_2000+408 others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92960705 | ||||||
| chr15:92960950 | G | A | 1 | a0001c0003t0003g0137 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2000+4301G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92960950 | |||||||
| chr15:92961271 | G | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(131): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2000+4622G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961271 | |||||||
| chr15:92961289 | A | AT | 250 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(247): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2000+4642dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961289 | ||||||
| chr15:92961441 | C | A | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2000+4792C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961441 | |||||||
| chr15:92961456 | G | A | 8 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0181 others(5): Show |
8 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.2000+4807G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961456 | |||||||
| chr15:92961824 | C | G | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2000+5175C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961824 | |||||||
| chr15:92961876 | C | CTT | 17 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(14): Show |
17 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2000+5249_2000+525 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961876 | ||||||
| chr15:92961876 | C | CTTTT | 15 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0069 others(12): Show |
15 | HG00099.hp1 HG00544.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.2000+5247_2000+525 others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961876 | ||||||
| chr15:92961876 | C | CTTTTT | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0027 others(121): Show |
127 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.2000+5246_2000+525 others(9): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961876 | ||||||
| chr15:92961876 | C | CTTTTTT | 21 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(18): Show |
22 | HG00738.hp2 HG01069.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.2000+5245_2000+525 others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961876 | ||||||
| chr15:92961876 | CTTTTTTT others(2): Show |
C | 60 | a0001c0001t0001g0016 a0001c0002t0001g0091 a0001c0002t0001g0233 others(57): Show |
60 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.2000+5242_2000+525 others(13): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92961876 | ||||||
| chr15:92961947 | T | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2000+5298T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961947 | |||||||
| chr15:92961950 | C | T | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.2000+5301C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92961950 | |||||||
| chr15:92962160 | G | A | 41 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(38): Show |
41 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.2001-5165G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962160 | |||||||
| chr15:92962354 | A | G | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2001-4971A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962354 | |||||||
| chr15:92962419 | T | G | 25 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(22): Show |
25 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.2001-4906T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962419 | |||||||
| chr15:92962545 | T | C | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2001-4780T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962545 | |||||||
| chr15:92962567 | T | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2001-4758T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962567 | |||||||
| chr15:92962651 | G | A | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2001-4674G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962651 | |||||||
| chr15:92962677 | T | TC | 22 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(19): Show |
22 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2001-4647dupC | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92962677 | ||||||
| chr15:92962854 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(127): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.2001-4471G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962854 | |||||||
| chr15:92962878 | T | C | 251 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2001-4447T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92962878 | |||||||
| chr15:92963002 | C | T | 1 | a0001c0002t0001g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2001-4323C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963002 | |||||||
| chr15:92963085 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2001-4240T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963085 | |||||||
| chr15:92963125 | G | T | 15 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(12): Show |
15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2001-4200G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963125 | |||||||
| chr15:92963443 | T | C | 22 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(19): Show |
22 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2001-3882T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963443 | |||||||
| chr15:92963475 | C | T | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
5 | NA18939.hp1 NA18944.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.2001-3850C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963475 | |||||||
| chr15:92963562 | T | C | 251 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2001-3763T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963562 | |||||||
| chr15:92963612 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2001-3713G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963612 | |||||||
| chr15:92963713 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0007g0174 a0001c0009t0002g0044 others(3): Show |
6 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2001-3612A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963713 | |||||||
| chr15:92963809 | T | C | 15 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(12): Show |
15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2001-3516T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963809 | |||||||
| chr15:92963831 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2001-3494A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92963831 | |||||||
| chr15:92964093 | T | G | 1 | a0001c0001t0020g0113 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2001-3232T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92964093 | |||||||
| chr15:92964231 | CT | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2001-3087delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92964231 | ||||||
| chr15:92964286 | C | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.2001-3039C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92964286 | |||||||
| chr15:92964312 | A | G | 1 | a0001c0001t0002g0278 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2001-3013A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92964312 | |||||||
| chr15:92964801 | G | A | 17 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(14): Show |
17 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.2001-2524G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92964801 | |||||||
| chr15:92964958 | A | G | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2001-2367A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92964958 | |||||||
| chr15:92965051 | C | T | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2001-2274C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965051 | |||||||
| chr15:92965107 | A | G | 1 | a0001c0004t0010g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2001-2218A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965107 | |||||||
| chr15:92965448 | CAGGAGGC others(5): Show |
C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2001-1876_2001-186 others(16): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965448 | |||||||
| chr15:92965512 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2001-1813C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965512 | |||||||
| chr15:92965565 | C | CA | 18 | a0001c0003t0001g0129 a0001c0003t0001g0144 a0001c0003t0002g0169 others(15): Show |
18 | HG00323.hp2 HG01109.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.2001-1730dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | C | CAA | 8 | a0001c0003t0001g0134 a0001c0003t0001g0141 a0001c0003t0003g0135 others(5): Show |
8 | HG00741.hp2 HG01243.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.2001-1731_2001-173 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | C | CAAAAAAA | 6 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0271 others(3): Show |
6 | HG01123.hp2 HG01192.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.2001-1736_2001-173 others(11): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0009g0010 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2001-1739_2001-173 others(14): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0009g0009 a0001c0001t0009g0011 |
2 | NA18967.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2001-1740_2001-173 others(15): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | CA | C | 6 | a0001c0001t0002g0294 a0001c0001t0002g0295 a0001c0001t0011g0292 others(3): Show |
6 | HG00738.hp2 HG01175.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.2001-1730delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | CAA | C | 18 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(15): Show |
18 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.2001-1731_2001-173 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | CAAA | C | 7 | a0001c0001t0007g0174 a0001c0002t0001g0091 a0001c0002t0002g0232 others(4): Show |
7 | HG00099.hp2 HG01975.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2001-1732_2001-173 others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | CAAAAA | C | 9 | a0001c0001t0001g0007 a0001c0001t0003g0274 a0001c0001t0005g0179 others(6): Show |
9 | HG00642.hp1 HG00673.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2001-1734_2001-173 others(9): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | CAAAAAA | C | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2001-1735_2001-173 others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | CAAAAAAA others(1): Show |
C | 11 | a0001c0001t0001g0259 a0001c0001t0006g0260 a0001c0001t0006g0261 others(8): Show |
11 | HG00735.hp2 HG01074.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.2001-1737_2001-173 others(12): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0070 a0001c0001t0008g0217 a0001c0019t0001g0119 |
3 | HG04204.hp2 NA18993.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.2001-1743_2001-173 others(18): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | CAAAAAAA others(8): Show |
C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2001-1744_2001-173 others(19): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965565 | CAAAAAAA others(10): Show |
C | 39 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0235 others(36): Show |
39 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.2001-1746_2001-173 others(21): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92965565 | ||||||
| chr15:92965591 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0007g0174 a0001c0009t0002g0044 others(3): Show |
6 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.2001-1734A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965591 | |||||||
| chr15:92965593 | A | AC | 3 | a0001c0003t0012g0126 a0001c0003t0012g0131 a0001c0003t0012g0132 |
3 | HG01257.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2001-1732_2001-173 others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965593 | |||||||
| chr15:92965617 | A | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2001-1708A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965617 | |||||||
| chr15:92965641 | C | T | 1 | a0001c0002t0001g0234 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2001-1684C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965641 | |||||||
| chr15:92965692 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2001-1633A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965692 | |||||||
| chr15:92965720 | A | G | 4 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
4 | HG02080.hp2 NA18953.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001-1605A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965720 | |||||||
| chr15:92965875 | A | C | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2001-1450A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965875 | |||||||
| chr15:92965913 | G | C | 9 | a0001c0002t0001g0235 a0001c0002t0001g0244 a0001c0002t0001g0247 others(6): Show |
9 | NA18939.hp2 NA18948.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.2001-1412G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965913 | |||||||
| chr15:92965930 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2001-1395C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965930 | |||||||
| chr15:92965952 | T | G | 1 | a0001c0001t0001g0212 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2001-1373T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92965952 | |||||||
| chr15:92966034 | T | C | 5 | a0001c0001t0001g0066 a0001c0001t0001g0070 a0001c0001t0001g0071 others(2): Show |
5 | NA18963.hp1 NA18968.hp2 NA18993.hp2 others(2): Show |
intron_variant | MODIFIER | c.2001-1291T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966034 | |||||||
| chr15:92966066 | C | CT | 7 | a0001c0001t0001g0081 a0001c0001t0009g0296 a0001c0002t0002g0046 others(4): Show |
7 | HG00639.hp1 HG00735.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.2001-1242dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92966066 | ||||||
| chr15:92966066 | CT | C | 16 | a0001c0001t0001g0078 a0001c0001t0001g0259 a0001c0001t0006g0253 others(13): Show |
16 | HG00735.hp2 HG01069.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2001-1242delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92966066 | ||||||
| chr15:92966144 | A | G | 4 | a0001c0001t0008g0217 a0001c0001t0008g0218 a0001c0001t0008g0219 others(1): Show |
4 | HG01361.hp1 HG03239.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001-1181A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966144 | |||||||
| chr15:92966238 | A | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2001-1087A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966238 | |||||||
| chr15:92966378 | T | A | 15 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(12): Show |
15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2001-947T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966378 | |||||||
| chr15:92966433 | G | C | 1 | a0001c0003t0003g0167 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2001-892G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966433 | |||||||
| chr15:92966576 | G | A | 6 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2001-749G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966576 | |||||||
| chr15:92966676 | C | T | 16 | a0001c0001t0001g0095 a0001c0001t0001g0259 a0001c0001t0006g0253 others(13): Show |
16 | HG00621.hp2 HG00735.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2001-649C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966676 | |||||||
| chr15:92966737 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2001-588C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966737 | |||||||
| chr15:92966866 | T | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2001-459T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966866 | |||||||
| chr15:92966889 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2001-436G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966889 | |||||||
| chr15:92966909 | C | CA | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2001-401dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | INFO_REALIGN_3_PRIME | chr15 | 92966909 | ||||||
| chr15:92966909 | C | T | 2 | a0001c0003t0002g0125 a0001c0003t0003g0137 |
2 | HG01069.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2001-416C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92966909 | |||||||
| chr15:92967013 | G | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.2001-312G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92967013 | |||||||
| chr15:92967161 | T | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2001-164T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 16/38 | chr15 | 92967161 | |||||||
| chr15:92967581 | T | C | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2189+68T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92967581 | |||||||
| chr15:92967598 | GT | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2189+99delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr15 | 92967598 | ||||||
| chr15:92967764 | G | T | 40 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(37): Show |
40 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.2189+251G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92967764 | |||||||
| chr15:92967992 | G | T | 2 | a0001c0001t0002g0278 a0001c0001t0002g0295 |
2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2189+479G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92967992 | |||||||
| chr15:92968014 | C | G | 15 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(12): Show |
15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2189+501C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968014 | |||||||
| chr15:92968041 | T | C | 1 | a0001c0009t0002g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2189+528T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968041 | |||||||
| chr15:92968063 | C | T | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2189+550C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968063 | |||||||
| chr15:92968112 | T | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2189+599T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968112 | |||||||
| chr15:92968119 | CA | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(131): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2189+608delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr15 | 92968119 | ||||||
| chr15:92968453 | A | C | 1 | a0001c0017t0009g0038 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2189+940A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968453 | |||||||
| chr15:92968524 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2189+1011C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968524 | |||||||
| chr15:92968618 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(247): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2189+1105T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968618 | |||||||
| chr15:92968953 | A | G | 1 | a0001c0002t0005g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2189+1440A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92968953 | |||||||
| chr15:92969384 | G | A | 1 | a0001c0018t0009g0036 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2189+1871G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969384 | |||||||
| chr15:92969448 | G | A | 232 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(229): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.2189+1935G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969448 | |||||||
| chr15:92969453 | C | T | 1 | a0001c0003t0001g0129 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2189+1940C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969453 | |||||||
| chr15:92969726 | A | G | 1 | a0001c0002t0001g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2190-2039A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969726 | |||||||
| chr15:92969749 | A | T | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-2016A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969749 | |||||||
| chr15:92969756 | C | A | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-2009C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969756 | |||||||
| chr15:92969812 | C | CT | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2190-1936dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr15 | 92969812 | ||||||
| chr15:92969812 | CT | C | 64 | a0001c0002t0001g0091 a0001c0002t0001g0233 a0001c0002t0001g0234 others(61): Show |
64 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.2190-1936delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr15 | 92969812 | ||||||
| chr15:92969825 | T | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2190-1940T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969825 | |||||||
| chr15:92969881 | A | C | 5 | a0001c0001t0001g0007 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2190-1884A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969881 | |||||||
| chr15:92969948 | A | G | 1 | a0001c0003t0008g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2190-1817A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92969948 | |||||||
| chr15:92970029 | T | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2190-1736T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970029 | |||||||
| chr15:92970283 | C | G | 2 | a0001c0003t0005g0124 a0001c0006t0005g0133 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2190-1482C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970283 | |||||||
| chr15:92970351 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2190-1414A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970351 | |||||||
| chr15:92970629 | A | G | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-1136A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970629 | |||||||
| chr15:92970835 | A | G | 1 | a0001c0001t0008g0217 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2190-930A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970835 | |||||||
| chr15:92970928 | A | G | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2190-837A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92970928 | |||||||
| chr15:92971018 | T | C | 2 | a0001c0003t0003g0172 a0001c0003t0003g0173 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2190-747T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971018 | |||||||
| chr15:92971143 | T | C | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2190-622T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971143 | |||||||
| chr15:92971192 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(130): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.2190-573T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971192 | |||||||
| chr15:92971234 | T | A | 1 | a0001c0001t0008g0219 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2190-531T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971234 | |||||||
| chr15:92971240 | C | A | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-525C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971240 | |||||||
| chr15:92971322 | G | C | 5 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2190-443G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971322 | |||||||
| chr15:92971445 | A | G | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-320A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971445 | |||||||
| chr15:92971449 | ATG | A | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-304_2190-303d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | INFO_REALIGN_3_PRIME | chr15 | 92971449 | ||||||
| chr15:92971503 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2190-262A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971503 | |||||||
| chr15:92971568 | T | A | 1 | a0001c0003t0003g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2190-197T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971568 | |||||||
| chr15:92971621 | C | G | 6 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(3): Show |
6 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2190-144C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971621 | |||||||
| chr15:92971642 | T | A | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2190-123T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971642 | |||||||
| chr15:92971674 | A | G | 9 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0181 others(6): Show |
9 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.2190-91A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971674 | |||||||
| chr15:92971706 | G | T | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2190-59G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 17/38 | chr15 | 92971706 | |||||||
| chr15:92972002 | A | C | 6 | a0001c0003t0002g0136 a0001c0003t0002g0162 a0001c0003t0002g0169 others(3): Show |
6 | HG02280.hp1 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2352+75A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 18/38 | chr15 | 92972002 | |||||||
| chr15:92972209 | G | A | 13 | a0001c0003t0001g0134 a0001c0003t0001g0141 a0001c0003t0001g0144 others(10): Show |
14 | HG00323.hp2 HG00741.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2353-56G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 18/38 | chr15 | 92972209 | |||||||
| chr15:92972456 | C | G | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2505+39C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92972456 | |||||||
| chr15:92972480 | A | C | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2505+63A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92972480 | |||||||
| chr15:92972557 | TAAGATTC others(306): Show |
T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2505+152_2505+464d others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | INFO_REALIGN_3_PRIME | chr15 | 92972557 | ||||||
| chr15:92972783 | G | A | 1 | a0001c0003t0003g0173 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2505+366G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92972783 | |||||||
| chr15:92972963 | G | T | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2505+546G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92972963 | |||||||
| chr15:92972986 | A | G | 2 | a0001c0005t0004g0153 a0001c0005t0004g0154 |
2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2505+569A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92972986 | |||||||
| chr15:92973019 | C | T | 1 | a0001c0003t0003g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2505+602C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973019 | |||||||
| chr15:92973121 | C | G | 2 | a0001c0005t0004g0153 a0001c0005t0004g0154 |
2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2505+704C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973121 | |||||||
| chr15:92973190 | C | T | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2505+773C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973190 | |||||||
| chr15:92973197 | A | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.2505+780A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973197 | |||||||
| chr15:92973266 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2505+849T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973266 | |||||||
| chr15:92973367 | C | T | 7 | a0001c0001t0001g0101 a0001c0001t0001g0178 a0001c0001t0001g0187 others(4): Show |
7 | HG01081.hp2 HG01261.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.2505+950C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973367 | |||||||
| chr15:92973544 | T | C | 1 | a0001c0001t0001g0007 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2505+1127T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973544 | |||||||
| chr15:92973564 | C | T | 2 | a0001c0001t0002g0008 a0001c0001t0002g0085 |
2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2505+1147C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973564 | |||||||
| chr15:92973681 | C | G | 40 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0235 others(37): Show |
40 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.2506-1198C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973681 | |||||||
| chr15:92973790 | G | A | 1 | a0001c0002t0001g0236 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2506-1089G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973790 | |||||||
| chr15:92973876 | T | C | 10 | a0001c0003t0001g0134 a0001c0003t0001g0141 a0001c0003t0001g0144 others(7): Show |
11 | HG00323.hp2 HG00741.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.2506-1003T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973876 | |||||||
| chr15:92973984 | G | A | 248 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2506-895G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92973984 | |||||||
| chr15:92974011 | A | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2506-868A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974011 | |||||||
| chr15:92974084 | A | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0087 |
2 | NA18973.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2506-795A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974084 | |||||||
| chr15:92974188 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2506-691G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974188 | |||||||
| chr15:92974192 | A | G | 15 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(12): Show |
15 | HG00642.hp2 HG00735.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.2506-687A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974192 | |||||||
| chr15:92974439 | G | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2506-440G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974439 | |||||||
| chr15:92974463 | T | C | 16 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(13): Show |
16 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2506-416T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974463 | |||||||
| chr15:92974718 | G | T | 1 | a0001c0002t0009g0243 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2506-161G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 19/38 | chr15 | 92974718 | |||||||
| chr15:92975209 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0023g0052 |
2 | NA18612.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.2577+259G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975209 | |||||||
| chr15:92975376 | C | T | 2 | a0001c0002t0011g0256 a0001c0002t0011g0257 |
2 | NA19000.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.2577+426C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975376 | |||||||
| chr15:92975426 | G | C | 2 | a0001c0002t0005g0230 a0001c0014t0005g0226 |
2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2577+476G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975426 | |||||||
| chr15:92975788 | A | G | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2577+838A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975788 | |||||||
| chr15:92975853 | TAATC | T | 248 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2577+904_2577+907d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975853 | |||||||
| chr15:92975877 | C | G | 248 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2577+927C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92975877 | |||||||
| chr15:92976153 | A | T | 51 | a0001c0001t0001g0016 a0001c0002t0001g0091 a0001c0002t0001g0233 others(48): Show |
51 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.2577+1203A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92976153 | |||||||
| chr15:92976186 | C | G | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2577+1236C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92976186 | |||||||
| chr15:92976191 | GA | G | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2577+1251delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | INFO_REALIGN_3_PRIME | chr15 | 92976191 | ||||||
| chr15:92976248 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2577+1298T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92976248 | |||||||
| chr15:92976581 | A | G | 1 | a0001c0003t0003g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2577+1631A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92976581 | |||||||
| chr15:92976653 | CA | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2578-1565delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | INFO_REALIGN_3_PRIME | chr15 | 92976653 | ||||||
| chr15:92976878 | G | A | 59 | a0001c0001t0001g0016 a0001c0002t0001g0091 a0001c0002t0001g0233 others(56): Show |
59 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.2578-1356G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92976878 | |||||||
| chr15:92976898 | CA | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.2578-1321delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | INFO_REALIGN_3_PRIME | chr15 | 92976898 | ||||||
| chr15:92977026 | A | C | 1 | a0001c0004t0004g0285 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2578-1208A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977026 | |||||||
| chr15:92977077 | A | G | 15 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(12): Show |
15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2578-1157A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977077 | |||||||
| chr15:92977183 | G | T | 3 | a0001c0003t0012g0126 a0001c0003t0012g0131 a0001c0003t0012g0132 |
3 | HG01257.hp1 HG01258.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2578-1051G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977183 | |||||||
| chr15:92977494 | A | G | 2 | a0001c0010t0002g0182 a0001c0010t0002g0222 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2578-740A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977494 | |||||||
| chr15:92977609 | T | C | 62 | a0001c0001t0001g0016 a0001c0001t0002g0293 a0001c0001t0002g0294 others(59): Show |
62 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.2578-625T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977609 | |||||||
| chr15:92977646 | C | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
103 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.2578-588C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977646 | |||||||
| chr15:92977652 | A | G | 2 | a0001c0003t0003g0175 a0001c0003t0003g0290 |
2 | HG01070.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2578-582A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 20/38 | chr15 | 92977652 | |||||||
| chr15:92978421 | T | G | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2727+38T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/38 | chr15 | 92978421 | |||||||
| chr15:92978428 | CA | C | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2727+46delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/38 | chr15 | 92978428 | |||||||
| chr15:92978750 | A | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2727+367A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/38 | chr15 | 92978750 | |||||||
| chr15:92979082 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2728-53G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/38 | chr15 | 92979082 | |||||||
| chr15:92979132 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19060.hp2 | splice_region_variant&intron_variant | LOW | c.2728-3C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 21/38 | chr15 | 92979132 | |||||||
| chr15:92979322 | T | C | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2876+39T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979322 | |||||||
| chr15:92979418 | A | G | 1 | a0001c0001t0008g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2876+135A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979418 | |||||||
| chr15:92979469 | C | A | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2876+186C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979469 | |||||||
| chr15:92979529 | T | C | 15 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(12): Show |
15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.2876+246T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979529 | |||||||
| chr15:92979619 | C | T | 14 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2876+336C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979619 | |||||||
| chr15:92979637 | G | GT | 15 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(12): Show |
16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.2876+366dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92979637 | ||||||
| chr15:92979896 | C | T | 6 | a0001c0001t0001g0007 a0001c0003t0008g0146 a0001c0009t0002g0044 others(3): Show |
6 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2876+613C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979896 | |||||||
| chr15:92979901 | G | GATA | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2876+634_2876+636d others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92979901 | ||||||
| chr15:92979977 | A | C | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2876+694A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92979977 | |||||||
| chr15:92980037 | T | TTTTG | 5 | a0001c0001t0001g0121 a0001c0002t0003g0227 a0001c0002t0005g0228 others(2): Show |
5 | HG01884.hp2 HG02451.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.2877-758_2877-755d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92980037 | ||||||
| chr15:92980037 | T | TTTTGTTT others(1): Show |
236 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(233): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2877-762_2877-755d others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92980037 | ||||||
| chr15:92980037 | T | TTTTGTTT others(5): Show |
8 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(5): Show |
9 | HG01069.hp1 HG01123.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.2876+766_2877-755d others(14): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92980037 | ||||||
| chr15:92980084 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2877-731G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980084 | |||||||
| chr15:92980222 | CT | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0029 a0001c0001t0001g0041 others(21): Show |
24 | HG00642.hp1 HG00673.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.2877-575delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92980222 | ||||||
| chr15:92980222 | CTT | C | 219 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2877-576_2877-575d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | INFO_REALIGN_3_PRIME | chr15 | 92980222 | ||||||
| chr15:92980224 | T | C | 3 | a0001c0001t0002g0278 a0001c0002t0005g0277 a0001c0002t0005g0279 |
3 | HG01167.hp2 HG01169.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2877-591T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980224 | |||||||
| chr15:92980271 | G | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.2877-544G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980271 | |||||||
| chr15:92980402 | A | G | 61 | a0001c0001t0001g0016 a0001c0001t0002g0293 a0001c0001t0002g0294 others(58): Show |
61 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.2877-413A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980402 | |||||||
| chr15:92980433 | G | A | 3 | a0001c0001t0009g0009 a0001c0001t0009g0010 a0001c0001t0009g0011 |
3 | NA18967.hp2 NA18994.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.2877-382G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980433 | |||||||
| chr15:92980477 | G | A | 9 | a0001c0002t0001g0235 a0001c0002t0001g0244 a0001c0002t0001g0247 others(6): Show |
9 | NA18939.hp2 NA18948.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.2877-338G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980477 | |||||||
| chr15:92980751 | A | G | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2877-64A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980751 | |||||||
| chr15:92980768 | T | G | 5 | a0001c0001t0001g0067 a0001c0001t0001g0082 a0001c0001t0001g0093 others(2): Show |
5 | HG00673.hp1 HG02155.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.2877-47T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 22/38 | chr15 | 92980768 | |||||||
| chr15:92980962 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2973+51G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92980962 | |||||||
| chr15:92980968 | A | G | 13 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0295 others(10): Show |
13 | HG00735.hp1 HG00738.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2973+57A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92980968 | |||||||
| chr15:92980972 | T | C | 15 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0002t0001g0091 others(12): Show |
15 | HG00099.hp2 HG00544.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.2973+61T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92980972 | |||||||
| chr15:92981082 | A | G | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2973+171A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92981082 | |||||||
| chr15:92981198 | T | G | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2974-167T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92981198 | |||||||
| chr15:92981300 | C | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0123 |
2 | NA18944.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.2974-65C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92981300 | |||||||
| chr15:92981309 | T | C | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.2974-56T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92981309 | |||||||
| chr15:92981315 | A | G | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2974-50A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 23/38 | chr15 | 92981315 | |||||||
| chr15:92981501 | T | G | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3066+44T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92981501 | |||||||
| chr15:92981619 | A | C | 2 | a0001c0003t0003g0175 a0001c0003t0003g0290 |
2 | HG01070.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3066+162A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92981619 | |||||||
| chr15:92981620 | G | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3066+163G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92981620 | |||||||
| chr15:92981637 | G | A | 51 | a0001c0002t0001g0091 a0001c0002t0001g0233 a0001c0002t0001g0234 others(48): Show |
51 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.3066+180G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92981637 | |||||||
| chr15:92981779 | A | G | 1 | a0001c0001t0002g0293 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.3066+322A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92981779 | |||||||
| chr15:92982120 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3066+663T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982120 | |||||||
| chr15:92982383 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0100 |
2 | HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.3066+926T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982383 | |||||||
| chr15:92982420 | G | A | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.3066+963G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982420 | |||||||
| chr15:92982636 | T | A | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3066+1179T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982636 | |||||||
| chr15:92982651 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3066+1194G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982651 | |||||||
| chr15:92982671 | T | C | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3066+1214T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982671 | |||||||
| chr15:92982773 | A | G | 70 | a0001c0001t0001g0016 a0001c0001t0002g0293 a0001c0001t0002g0294 others(67): Show |
70 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.3066+1316A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982773 | |||||||
| chr15:92982869 | G | A | 5 | a0001c0001t0007g0174 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.3066+1412G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982869 | |||||||
| chr15:92982878 | G | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3066+1421G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92982878 | |||||||
| chr15:92983008 | T | C | 2 | a0001c0002t0003g0227 a0001c0002t0005g0228 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3067-1322T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983008 | |||||||
| chr15:92983135 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0007g0174 a0001c0009t0002g0044 others(3): Show |
6 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3067-1195A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983135 | |||||||
| chr15:92983219 | A | G | 1 | a0001c0001t0008g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3067-1111A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983219 | |||||||
| chr15:92983300 | A | C | 1 | a0001c0016t0002g0047 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3067-1030A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983300 | |||||||
| chr15:92983651 | C | T | 2 | a0001c0008t0001g0127 a0001c0008t0001g0145 |
2 | HG00323.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3067-679C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983651 | |||||||
| chr15:92983663 | T | G | 62 | a0001c0001t0001g0016 a0001c0001t0002g0293 a0001c0001t0002g0294 others(59): Show |
62 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.3067-667T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983663 | |||||||
| chr15:92983671 | G | A | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3067-659G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983671 | |||||||
| chr15:92983738 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(233): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.3067-592A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983738 | |||||||
| chr15:92983808 | C | T | 5 | a0001c0001t0001g0007 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.3067-522C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92983808 | |||||||
| chr15:92984166 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3067-164G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 24/38 | chr15 | 92984166 | |||||||
| chr15:92984564 | A | T | 59 | a0001c0001t0001g0016 a0001c0002t0001g0091 a0001c0002t0001g0233 others(56): Show |
59 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3237+64A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984564 | |||||||
| chr15:92984613 | G | A | 234 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.3237+113G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984613 | |||||||
| chr15:92984629 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3237+129T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984629 | |||||||
| chr15:92984650 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3237+150A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984650 | |||||||
| chr15:92984758 | G | C | 59 | a0001c0001t0001g0016 a0001c0002t0001g0091 a0001c0002t0001g0233 others(56): Show |
59 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.3237+258G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984758 | |||||||
| chr15:92984785 | C | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(74): Show |
78 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.3237+285C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984785 | |||||||
| chr15:92984823 | A | G | 8 | a0001c0001t0001g0007 a0001c0001t0007g0174 a0001c0009t0002g0044 others(5): Show |
8 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3237+323A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984823 | |||||||
| chr15:92984824 | G | A | 4 | a0001c0002t0008g0015 a0001c0004t0007g0020 a0001c0004t0017g0019 others(1): Show |
4 | HG01070.hp2 HG01123.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.3237+324G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92984824 | |||||||
| chr15:92985222 | A | G | 2 | a0001c0002t0003g0227 a0001c0002t0005g0228 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3238-276A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92985222 | |||||||
| chr15:92985243 | T | C | 224 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.3238-255T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 25/38 | chr15 | 92985243 | |||||||
| chr15:92985689 | G | A | 5 | a0001c0003t0003g0161 a0001c0003t0003g0167 a0001c0003t0003g0171 others(2): Show |
5 | HG01109.hp2 HG01884.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.3413+16G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92985689 | |||||||
| chr15:92985715 | C | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3413+42C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92985715 | |||||||
| chr15:92985716 | G | A | 4 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0005g0224 others(1): Show |
4 | HG02572.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3413+43G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92985716 | |||||||
| chr15:92986482 | G | C | 1 | a0001c0001t0008g0040 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3413+809G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986482 | |||||||
| chr15:92986496 | TACTG | T | 4 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0005g0224 others(1): Show |
4 | HG02572.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3413+826_3413+829d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92986496 | ||||||
| chr15:92986510 | C | T | 2 | a0001c0004t0007g0018 a0001c0004t0007g0021 |
2 | HG01433.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.3413+837C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986510 | |||||||
| chr15:92986785 | A | G | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3413+1112A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986785 | |||||||
| chr15:92986906 | T | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3413+1233T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986906 | |||||||
| chr15:92986952 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG00438.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.3413+1279G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986952 | |||||||
| chr15:92986989 | G | C | 1 | a0001c0002t0001g0248 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3413+1316G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92986989 | |||||||
| chr15:92987029 | C | T | 1 | a0001c0003t0003g0290 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3413+1356C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987029 | |||||||
| chr15:92987030 | G | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.3413+1357G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987030 | |||||||
| chr15:92987137 | G | A | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3413+1464G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987137 | |||||||
| chr15:92987185 | G | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.3413+1512G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987185 | |||||||
| chr15:92987319 | C | A | 1 | a0001c0002t0016g0280 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3413+1646C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987319 | |||||||
| chr15:92987335 | C | T | 1 | a0001c0003t0003g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3413+1662C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987335 | |||||||
| chr15:92987473 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(131): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3413+1800C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987473 | |||||||
| chr15:92987616 | GA | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.3413+1956delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92987616 | ||||||
| chr15:92987781 | T | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3413+2108T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987781 | |||||||
| chr15:92987800 | A | G | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3413+2127A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987800 | |||||||
| chr15:92987806 | C | T | 2 | a0001c0002t0003g0227 a0001c0002t0005g0228 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3413+2133C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987806 | |||||||
| chr15:92987857 | T | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(250): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.3413+2184T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92987857 | |||||||
| chr15:92988011 | C | T | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3413+2338C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988011 | |||||||
| chr15:92988082 | CT | C | 51 | a0001c0002t0001g0091 a0001c0002t0001g0233 a0001c0002t0001g0234 others(48): Show |
51 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.3413+2421delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92988082 | ||||||
| chr15:92988105 | G | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3413+2432G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988105 | |||||||
| chr15:92988245 | C | T | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3413+2572C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988245 | |||||||
| chr15:92988484 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.3413+2811C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988484 | |||||||
| chr15:92988568 | G | A | 4 | a0001c0009t0002g0044 a0001c0009t0002g0048 a0001c0009t0012g0043 others(1): Show |
4 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.3413+2895G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988568 | |||||||
| chr15:92988594 | A | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3414-2882A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988594 | |||||||
| chr15:92988640 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3414-2836A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988640 | |||||||
| chr15:92988677 | A | T | 1 | a0001c0014t0005g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3414-2799A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988677 | |||||||
| chr15:92988777 | A | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3414-2699A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92988777 | |||||||
| chr15:92989025 | CT | C | 88 | a0001c0001t0001g0016 a0001c0001t0001g0072 a0001c0001t0001g0259 others(85): Show |
88 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.3414-2428delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92989025 | ||||||
| chr15:92989025 | CTT | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.3414-2429_3414-242 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92989025 | ||||||
| chr15:92989025 | CTTT | C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(13): Show |
17 | HG01123.hp2 HG01192.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3414-2430_3414-242 others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92989025 | ||||||
| chr15:92989141 | C | A | 4 | a0001c0001t0024g0074 a0001c0005t0007g0050 a0001c0005t0007g0090 others(1): Show |
4 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.3414-2335C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92989141 | |||||||
| chr15:92989321 | C | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3414-2155C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92989321 | |||||||
| chr15:92989520 | T | C | 1 | a0001c0003t0003g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3414-1956T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92989520 | |||||||
| chr15:92989877 | C | T | 16 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0295 others(13): Show |
16 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.3414-1599C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92989877 | |||||||
| chr15:92989970 | C | T | 9 | a0001c0002t0002g0156 a0001c0002t0002g0231 a0001c0002t0003g0227 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3414-1506C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92989970 | |||||||
| chr15:92990035 | G | A | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3414-1441G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990035 | |||||||
| chr15:92990181 | C | G | 1 | a0001c0001t0006g0264 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3414-1295C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990181 | |||||||
| chr15:92990316 | T | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3414-1160T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990316 | |||||||
| chr15:92990341 | C | T | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3414-1135C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990341 | |||||||
| chr15:92990392 | C | T | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3414-1084C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990392 | |||||||
| chr15:92990716 | C | T | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3414-760C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990716 | |||||||
| chr15:92990875 | G | A | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3414-601G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92990875 | |||||||
| chr15:92991147 | GAC | G | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3414-325_3414-324d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | INFO_REALIGN_3_PRIME | chr15 | 92991147 | ||||||
| chr15:92991222 | C | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(125): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.3414-254C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 26/38 | chr15 | 92991222 | |||||||
| chr15:92991703 | A | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.3455+186A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92991703 | |||||||
| chr15:92991708 | G | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3455+191G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92991708 | |||||||
| chr15:92991709 | A | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3455+192A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92991709 | |||||||
| chr15:92991964 | G | A | 5 | a0001c0001t0007g0174 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.3455+447G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92991964 | |||||||
| chr15:92992150 | A | C | 1 | a0001c0002t0009g0022 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3455+633A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992150 | |||||||
| chr15:92992263 | A | G | 1 | a0001c0003t0005g0166 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3456-596A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992263 | |||||||
| chr15:92992323 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3456-536C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992323 | |||||||
| chr15:92992467 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3456-392A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992467 | |||||||
| chr15:92992560 | C | T | 1 | a0001c0001t0002g0085 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3456-299C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992560 | |||||||
| chr15:92992725 | A | G | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3456-134A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992725 | |||||||
| chr15:92992843 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3456-16A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 27/38 | chr15 | 92992843 | |||||||
| chr15:92993049 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3595+51G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993049 | |||||||
| chr15:92993174 | C | T | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3595+176C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993174 | |||||||
| chr15:92993219 | T | C | 1 | a0001c0001t0006g0268 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3595+221T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993219 | |||||||
| chr15:92993394 | A | C | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3595+396A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993394 | |||||||
| chr15:92993396 | G | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3595+398G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993396 | |||||||
| chr15:92993436 | G | A | 234 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.3595+438G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993436 | |||||||
| chr15:92993440 | C | A | 1 | a0001c0003t0003g0171 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3595+442C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993440 | |||||||
| chr15:92993568 | A | AAGATATA others(7): Show |
79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(76): Show |
80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3595+572_3595+573i others(16): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr15 | 92993568 | ||||||
| chr15:92993571 | C | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(76): Show |
80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3595+573C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993571 | |||||||
| chr15:92993574 | G | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(76): Show |
80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3595+576G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993574 | |||||||
| chr15:92993578 | T | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(76): Show |
80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3595+580T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993578 | |||||||
| chr15:92993581 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0027 others(76): Show |
80 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.3595+583A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993581 | |||||||
| chr15:92993635 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.3595+637T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993635 | |||||||
| chr15:92993680 | C | G | 71 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0002t0001g0091 others(68): Show |
71 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.3595+682C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993680 | |||||||
| chr15:92993769 | G | A | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3595+771G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993769 | |||||||
| chr15:92993806 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3595+808A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993806 | |||||||
| chr15:92993839 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3595+841A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993839 | |||||||
| chr15:92993883 | GGCTGCAG others(17): Show |
G | 1 | a0001c0002t0001g0239 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.3595+910_3595+933d others(26): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr15 | 92993883 | ||||||
| chr15:92993938 | C | T | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3595+940C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92993938 | |||||||
| chr15:92994149 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3595+1151G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994149 | |||||||
| chr15:92994418 | A | G | 1 | a0001c0004t0007g0018 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3595+1420A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994418 | |||||||
| chr15:92994589 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3595+1591T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994589 | |||||||
| chr15:92994632 | A | G | 1 | a0001c0002t0002g0275 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3595+1634A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994632 | |||||||
| chr15:92994687 | G | A | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3595+1689G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994687 | |||||||
| chr15:92994728 | G | A | 56 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0002t0001g0091 others(53): Show |
56 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.3595+1730G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994728 | |||||||
| chr15:92994886 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3595+1888T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994886 | |||||||
| chr15:92994900 | T | C | 1 | a0001c0001t0006g0268 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3595+1902T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92994900 | |||||||
| chr15:92995200 | C | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.3596-1757C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995200 | |||||||
| chr15:92995246 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3596-1711C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995246 | |||||||
| chr15:92995299 | C | T | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3596-1658C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995299 | |||||||
| chr15:92995421 | T | C | 64 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0002t0001g0091 others(61): Show |
64 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.3596-1536T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995421 | |||||||
| chr15:92995427 | G | T | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3596-1530G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995427 | |||||||
| chr15:92995452 | T | C | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3596-1505T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995452 | |||||||
| chr15:92995491 | CGTGT | C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
152 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.3596-1463_3596-146 others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr15 | 92995491 | ||||||
| chr15:92995653 | CT | C | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3596-1303delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995653 | |||||||
| chr15:92995776 | G | T | 3 | a0001c0001t0001g0007 a0001c0009t0002g0048 a0001c0016t0002g0047 |
3 | HG00642.hp1 HG00673.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.3596-1181G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995776 | |||||||
| chr15:92995814 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.3596-1143C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995814 | |||||||
| chr15:92995861 | A | G | 2 | a0001c0009t0002g0044 a0001c0009t0012g0043 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.3596-1096A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92995861 | |||||||
| chr15:92996160 | C | CT | 15 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0035 others(12): Show |
16 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.3596-780dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr15 | 92996160 | ||||||
| chr15:92996160 | CT | C | 148 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0130 others(145): Show |
150 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.3596-780delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | INFO_REALIGN_3_PRIME | chr15 | 92996160 | ||||||
| chr15:92996190 | C | T | 4 | a0001c0003t0003g0139 a0001c0003t0003g0170 a0001c0010t0002g0182 others(1): Show |
4 | HG02486.hp2 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3596-767C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996190 | |||||||
| chr15:92996191 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0007g0174 a0001c0009t0002g0044 others(3): Show |
6 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3596-766G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996191 | |||||||
| chr15:92996251 | C | A | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3596-706C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996251 | |||||||
| chr15:92996378 | T | G | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3596-579T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996378 | |||||||
| chr15:92996395 | C | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(131): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3596-562C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996395 | |||||||
| chr15:92996436 | A | T | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(131): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.3596-521A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996436 | |||||||
| chr15:92996730 | C | G | 2 | a0001c0003t0001g0129 a0001c0006t0004g0163 |
2 | HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3596-227C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996730 | |||||||
| chr15:92996759 | C | A | 2 | a0001c0005t0004g0153 a0001c0005t0004g0154 |
2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3596-198C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996759 | |||||||
| chr15:92996859 | T | C | 63 | a0001c0001t0001g0016 a0001c0001t0002g0293 a0001c0001t0002g0294 others(60): Show |
63 | HG00099.hp2 HG00423.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.3596-98T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996859 | |||||||
| chr15:92996937 | G | A | 6 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0005g0224 others(3): Show |
6 | HG01243.hp2 HG02572.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.3596-20G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 28/38 | chr15 | 92996937 | |||||||
| chr15:92997526 | G | A | 2 | a0001c0005t0004g0153 a0001c0005t0004g0154 |
2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3885+123G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997526 | |||||||
| chr15:92997538 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3885+135A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997538 | |||||||
| chr15:92997699 | T | C | 5 | a0001c0001t0001g0007 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.3885+296T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997699 | |||||||
| chr15:92997702 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3885+299A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997702 | |||||||
| chr15:92997767 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.3885+364C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997767 | |||||||
| chr15:92997892 | A | G | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3885+489A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997892 | |||||||
| chr15:92997959 | A | AC | 237 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(234): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.3886-540_3886-539i others(3): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92997959 | |||||||
| chr15:92998479 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.3886-20C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 30/38 | chr15 | 92998479 | |||||||
| chr15:92998719 | A | G | 1 | a0001c0003t0003g0175 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.4008+98A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998719 | |||||||
| chr15:92998723 | T | G | 1 | a0001c0001t0001g0027 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4008+102T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998723 | |||||||
| chr15:92998769 | G | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4008+148G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998769 | |||||||
| chr15:92998770 | C | G | 250 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(247): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.4008+149C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998770 | |||||||
| chr15:92998849 | T | C | 235 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.4008+228T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998849 | |||||||
| chr15:92998858 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(127): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.4008+237C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998858 | |||||||
| chr15:92998879 | T | C | 1 | a0001c0004t0010g0106 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4008+258T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998879 | |||||||
| chr15:92998941 | G | A | 1 | a0001c0005t0004g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4008+320G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998941 | |||||||
| chr15:92998961 | GTAATCCC others(9): Show |
G | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4008+341_4008+356d others(18): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998961 | |||||||
| chr15:92998987 | G | A | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4008+366G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92998987 | |||||||
| chr15:92999051 | T | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(127): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.4008+430T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999051 | |||||||
| chr15:92999083 | C | CA | 21 | a0001c0003t0001g0129 a0001c0003t0002g0125 a0001c0003t0002g0136 others(18): Show |
22 | HG01069.hp2 HG01243.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.4008+496dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | C | CAA | 6 | a0001c0003t0002g0162 a0001c0003t0003g0167 a0001c0003t0003g0171 others(3): Show |
6 | HG01109.hp2 HG01884.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.4008+495_4008+496d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4008+485_4008+496d others(14): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | C | CAAAAAAA others(8): Show |
1 | a0001c0005t0004g0287 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4008+482_4008+496d others(17): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | C | CAAAAAAA others(13): Show |
1 | a0001c0005t0004g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4008+477_4008+496d others(22): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | CA | C | 9 | a0001c0001t0002g0278 a0001c0003t0001g0144 a0001c0003t0003g0128 others(6): Show |
10 | HG00323.hp2 HG01070.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.4008+496delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | CAAA | C | 6 | a0001c0001t0002g0294 a0001c0001t0006g0264 a0001c0001t0006g0270 others(3): Show |
6 | HG00642.hp1 HG01361.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4008+494_4008+496d others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | CAAAA | C | 25 | a0001c0001t0001g0259 a0001c0001t0002g0293 a0001c0001t0006g0253 others(22): Show |
25 | HG00544.hp1 HG00639.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.4008+493_4008+496d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | CAAAAA | C | 52 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0006g0266 others(49): Show |
52 | HG00099.hp2 HG00558.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.4008+492_4008+496d others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | CAAAAAA | C | 9 | a0001c0001t0001g0207 a0001c0001t0009g0009 a0001c0001t0009g0011 others(6): Show |
9 | HG00423.hp2 HG03453.hp1 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.4008+491_4008+496d others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | CAAAAAAA | C | 26 | a0001c0001t0001g0006 a0001c0001t0001g0034 a0001c0001t0001g0035 others(23): Show |
27 | HG00423.hp1 HG01069.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.4008+490_4008+496d others(9): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | CAAAAAAA others(1): Show |
C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(112): Show |
118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.4008+489_4008+496d others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999083 | CAAAAAAA others(7): Show |
C | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4008+483_4008+496d others(16): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | INFO_REALIGN_3_PRIME | chr15 | 92999083 | ||||||
| chr15:92999214 | C | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4008+593C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999214 | |||||||
| chr15:92999279 | C | T | 1 | a0001c0002t0001g0286 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4008+658C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999279 | |||||||
| chr15:92999365 | T | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0259 a0001c0001t0006g0253 others(23): Show |
26 | HG00642.hp1 HG00673.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.4008+744T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999365 | |||||||
| chr15:92999683 | C | T | 2 | a0001c0002t0003g0227 a0001c0002t0005g0228 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.4009-829C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999683 | |||||||
| chr15:92999698 | A | T | 6 | a0001c0001t0001g0007 a0001c0001t0007g0174 a0001c0009t0002g0044 others(3): Show |
6 | HG00642.hp1 HG00673.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.4009-814A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999698 | |||||||
| chr15:92999705 | G | T | 41 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0001c0002t0001g0235 others(38): Show |
41 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.4009-807G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999705 | |||||||
| chr15:92999712 | A | G | 15 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(12): Show |
15 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.4009-800A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999712 | |||||||
| chr15:92999812 | A | G | 13 | a0001c0003t0001g0134 a0001c0003t0001g0141 a0001c0003t0001g0144 others(10): Show |
14 | HG00323.hp2 HG00741.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.4009-700A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999812 | |||||||
| chr15:92999907 | A | T | 2 | a0001c0001t0003g0274 a0001c0001t0005g0179 |
2 | NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4009-605A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 92999907 | |||||||
| chr15:93000057 | G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4009-455G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 93000057 | |||||||
| chr15:93000301 | A | T | 59 | a0001c0001t0001g0016 a0001c0002t0001g0091 a0001c0002t0001g0233 others(56): Show |
59 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.4009-211A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 31/38 | chr15 | 93000301 | |||||||
| chr15:93000677 | A | G | 1 | a0001c0004t0007g0017 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4137+37A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000677 | |||||||
| chr15:93000726 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(130): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.4137+86G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000726 | |||||||
| chr15:93000782 | G | A | 1 | a0001c0003t0012g0131 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4137+142G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000782 | |||||||
| chr15:93000821 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4137+181A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000821 | |||||||
| chr15:93000823 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(130): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.4137+183A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000823 | |||||||
| chr15:93000873 | T | C | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4137+233T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000873 | |||||||
| chr15:93000893 | A | G | 2 | a0001c0005t0004g0153 a0001c0005t0004g0154 |
2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4137+253A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000893 | |||||||
| chr15:93000909 | G | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4137+269G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93000909 | |||||||
| chr15:93001041 | G | A | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4137+401G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001041 | |||||||
| chr15:93001216 | C | G | 6 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0024g0074 others(3): Show |
6 | HG00099.hp1 HG00140.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.4137+576C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001216 | |||||||
| chr15:93001223 | C | T | 1 | a0001c0001t0006g0080 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.4137+583C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001223 | |||||||
| chr15:93001376 | A | G | 1 | a0001c0003t0008g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4137+736A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001376 | |||||||
| chr15:93001466 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(234): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.4138-711T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001466 | |||||||
| chr15:93001999 | A | G | 1 | a0001c0005t0007g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4138-178A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93001999 | |||||||
| chr15:93002018 | G | A | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4138-159G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93002018 | |||||||
| chr15:93002105 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4138-72T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93002105 | |||||||
| chr15:93002118 | A | G | 1 | a0001c0001t0024g0074 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4138-59A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93002118 | |||||||
| chr15:93002145 | G | A | 1 | a0001c0001t0024g0074 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4138-32G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93002145 | |||||||
| chr15:93002162 | T | G | 5 | a0001c0001t0001g0007 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.4138-15T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 32/38 | chr15 | 93002162 | |||||||
| chr15:93002344 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4278+27A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002344 | |||||||
| chr15:93002369 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4278+52A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002369 | |||||||
| chr15:93002523 | A | G | 1 | a0001c0003t0003g0147 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4278+206A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002523 | |||||||
| chr15:93002601 | G | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4278+284G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002601 | |||||||
| chr15:93002619 | C | T | 1 | a0001c0004t0004g0297 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4278+302C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002619 | |||||||
| chr15:93002704 | T | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(144): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.4278+387T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002704 | |||||||
| chr15:93002717 | T | C | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4278+400T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002717 | |||||||
| chr15:93002843 | TA | T | 5 | a0001c0002t0002g0231 a0001c0002t0005g0220 a0001c0002t0005g0229 others(2): Show |
5 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.4278+530delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93002843 | ||||||
| chr15:93002862 | C | A | 1 | a0001c0014t0005g0226 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4278+545C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002862 | |||||||
| chr15:93002866 | C | T | 5 | a0001c0001t0001g0007 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.4278+549C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93002866 | |||||||
| chr15:93003089 | G | GCAAC | 14 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(11): Show |
15 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.4278+773_4278+776d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003089 | ||||||
| chr15:93003163 | C | T | 1 | a0001c0003t0002g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4278+846C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003163 | |||||||
| chr15:93003244 | C | G | 55 | a0001c0001t0001g0016 a0001c0002t0001g0091 a0001c0002t0001g0233 others(52): Show |
55 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.4278+927C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003244 | |||||||
| chr15:93003286 | C | CA | 51 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0002g0293 others(48): Show |
51 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.4278+988dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003286 | ||||||
| chr15:93003286 | CA | C | 24 | a0001c0001t0001g0079 a0001c0001t0001g0210 a0001c0001t0002g0278 others(21): Show |
24 | HG00099.hp2 HG01070.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.4278+988delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003286 | ||||||
| chr15:93003286 | CAA | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(139): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4278+987_4278+988d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003286 | ||||||
| chr15:93003286 | CAAA | C | 22 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(19): Show |
23 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.4278+986_4278+988d others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003286 | ||||||
| chr15:93003309 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(128): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.4278+992T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003309 | |||||||
| chr15:93003412 | C | G | 13 | a0001c0001t0001g0007 a0001c0001t0007g0174 a0001c0002t0002g0231 others(10): Show |
13 | HG00642.hp1 HG00673.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.4278+1095C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003412 | |||||||
| chr15:93003445 | C | T | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4278+1128C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003445 | |||||||
| chr15:93003577 | C | CT | 13 | a0001c0001t0001g0081 a0001c0002t0001g0091 a0001c0002t0001g0247 others(10): Show |
13 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.4279-1025dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93003577 | ||||||
| chr15:93003604 | G | T | 1 | a0001c0001t0001g0067 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4279-1013G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93003604 | |||||||
| chr15:93004073 | G | A | 25 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(22): Show |
25 | HG00642.hp1 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.4279-544G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004073 | |||||||
| chr15:93004083 | C | T | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4279-534C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004083 | |||||||
| chr15:93004107 | G | C | 15 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0002t0001g0091 others(12): Show |
15 | HG00099.hp2 HG00544.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.4279-510G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004107 | |||||||
| chr15:93004110 | C | T | 1 | a0001c0001t0007g0174 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4279-507C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004110 | |||||||
| chr15:93004123 | C | CA | 44 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(41): Show |
45 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.4279-475dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93004123 | ||||||
| chr15:93004123 | C | CAA | 11 | a0001c0001t0007g0174 a0001c0002t0002g0231 a0001c0002t0005g0220 others(8): Show |
11 | HG00642.hp1 HG00673.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.4279-476_4279-475d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | INFO_REALIGN_3_PRIME | chr15 | 93004123 | ||||||
| chr15:93004345 | T | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(220): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.4279-272T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004345 | |||||||
| chr15:93004495 | T | TC | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4279-122_4279-121i others(3): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004495 | |||||||
| chr15:93004496 | T | A | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4279-121T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004496 | |||||||
| chr15:93004564 | G | A | 1 | a0001c0002t0001g0249 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4279-53G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 33/38 | chr15 | 93004564 | |||||||
| chr15:93004766 | C | T | 2 | a0001c0001t0002g0008 a0001c0001t0002g0085 |
2 | HG02257.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.4413+15C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93004766 | |||||||
| chr15:93004789 | C | T | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4413+38C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93004789 | |||||||
| chr15:93005292 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4413+541G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005292 | |||||||
| chr15:93005373 | G | T | 1 | a0001c0002t0001g0091 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4413+622G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005373 | |||||||
| chr15:93005417 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4413+666C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005417 | |||||||
| chr15:93005448 | C | T | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4413+697C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005448 | |||||||
| chr15:93005477 | G | C | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4413+726G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005477 | |||||||
| chr15:93005534 | GA | G | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4413+786delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr15 | 93005534 | ||||||
| chr15:93005567 | A | G | 2 | a0001c0002t0002g0275 a0001c0002t0016g0280 |
2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.4413+816A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005567 | |||||||
| chr15:93005632 | T | G | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4413+881T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005632 | |||||||
| chr15:93005998 | A | T | 5 | a0001c0001t0009g0296 a0001c0001t0011g0282 a0001c0001t0011g0292 others(2): Show |
5 | HG00735.hp1 HG01074.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.4413+1247A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93005998 | |||||||
| chr15:93006124 | C | CT | 57 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0057 others(54): Show |
57 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.4413+1393dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr15 | 93006124 | ||||||
| chr15:93006125 | T | TC | 6 | a0001c0003t0002g0136 a0001c0003t0002g0162 a0001c0003t0002g0169 others(3): Show |
6 | HG02280.hp1 HG02922.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.4413+1374_4413+137 others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006125 | |||||||
| chr15:93006126 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0177 |
2 | NA18979.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.4413+1375T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006126 | |||||||
| chr15:93006127 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0112 |
2 | NA18939.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.4413+1376T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006127 | |||||||
| chr15:93006157 | T | G | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4413+1406T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006157 | |||||||
| chr15:93006195 | C | T | 4 | a0001c0001t0001g0007 a0001c0009t0002g0044 a0001c0009t0002g0048 others(1): Show |
4 | HG00673.hp2 HG02258.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.4413+1444C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006195 | |||||||
| chr15:93006433 | C | G | 42 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(39): Show |
42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.4413+1682C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006433 | |||||||
| chr15:93006603 | C | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.4413+1852C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006603 | |||||||
| chr15:93006736 | A | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.4413+1985A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93006736 | |||||||
| chr15:93007120 | G | A | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4414-2025G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007120 | |||||||
| chr15:93007139 | T | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4414-2006T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007139 | |||||||
| chr15:93007334 | A | C | 1 | a0001c0001t0001g0115 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.4414-1811A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007334 | |||||||
| chr15:93007350 | T | C | 42 | a0001c0001t0001g0016 a0001c0002t0001g0233 a0001c0002t0001g0234 others(39): Show |
42 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.4414-1795T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007350 | |||||||
| chr15:93007720 | TTACC | T | 170 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(167): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.4414-1423_4414-142 others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr15 | 93007720 | ||||||
| chr15:93007750 | A | G | 7 | a0001c0002t0002g0231 a0001c0002t0003g0227 a0001c0002t0005g0220 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4414-1395A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007750 | |||||||
| chr15:93007878 | C | T | 170 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(167): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.4414-1267C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93007878 | |||||||
| chr15:93007911 | TC | T | 2 | a0001c0001t0001g0026 a0001c0001t0003g0001 |
3 | HG01515.hp2 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4414-1232delC | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | INFO_REALIGN_3_PRIME | chr15 | 93007911 | ||||||
| chr15:93008063 | G | C | 10 | a0001c0002t0001g0091 a0001c0002t0001g0286 a0001c0002t0002g0275 others(7): Show |
10 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.4414-1082G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008063 | |||||||
| chr15:93008116 | G | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(131): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.4414-1029G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008116 | |||||||
| chr15:93008165 | G | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4414-980G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008165 | |||||||
| chr15:93008289 | C | T | 3 | a0001c0002t0002g0223 a0001c0002t0005g0224 a0001c0002t0005g0225 |
3 | HG02572.hp2 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4414-856C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008289 | |||||||
| chr15:93008317 | C | T | 170 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(167): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.4414-828C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008317 | |||||||
| chr15:93008454 | C | T | 2 | a0001c0002t0002g0275 a0001c0002t0016g0280 |
2 | HG00099.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.4414-691C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008454 | |||||||
| chr15:93008470 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.4414-675C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008470 | |||||||
| chr15:93008521 | C | G | 1 | a0001c0005t0004g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4414-624C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008521 | |||||||
| chr15:93008570 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4414-575G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008570 | |||||||
| chr15:93008573 | C | T | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4414-572C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008573 | |||||||
| chr15:93008623 | G | T | 4 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0005g0224 others(1): Show |
4 | HG02572.hp2 HG03209.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.4414-522G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008623 | |||||||
| chr15:93008746 | A | C | 6 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0005g0224 others(3): Show |
6 | HG01243.hp2 HG02572.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.4414-399A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008746 | |||||||
| chr15:93008995 | C | G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG03492.hp2 HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4414-150C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008995 | |||||||
| chr15:93008999 | C | A | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4414-146C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93008999 | |||||||
| chr15:93009100 | C | T | 249 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4414-45C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93009100 | |||||||
| chr15:93009119 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0001g0078 others(1): Show |
5 | HG01167.hp1 HG01192.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.4414-26G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 34/38 | chr15 | 93009119 | |||||||
| chr15:93009426 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(247): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.4592+103C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009426 | |||||||
| chr15:93009501 | G | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4592+178G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009501 | |||||||
| chr15:93009545 | T | G | 1 | a0001c0001t0001g0298 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4592+222T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009545 | |||||||
| chr15:93009701 | A | G | 14 | a0001c0001t0001g0259 a0001c0001t0006g0084 a0001c0001t0006g0253 others(11): Show |
14 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.4592+378A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009701 | |||||||
| chr15:93009735 | A | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(10): Show |
14 | HG01069.hp1 HG01123.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.4592+412A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009735 | |||||||
| chr15:93009738 | G | T | 1 | a0001c0001t0001g0299 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4592+415G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009738 | |||||||
| chr15:93009898 | A | G | 14 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0002t0001g0091 others(11): Show |
15 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.4592+575A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93009898 | |||||||
| chr15:93010317 | G | T | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4592+994G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010317 | |||||||
| chr15:93010319 | CTTCTT | C | 38 | a0001c0001t0001g0016 a0001c0001t0020g0113 a0001c0002t0001g0234 others(35): Show |
38 | HG00558.hp1 HG00621.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.4592+1000_4592+100 others(9): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 93010319 | ||||||
| chr15:93010410 | A | AT | 13 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(10): Show |
13 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4592+1108dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 93010410 | ||||||
| chr15:93010410 | ATTT | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(170): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.4592+1106_4592+110 others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 93010410 | ||||||
| chr15:93010410 | ATTTT | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0056 a0001c0001t0001g0093 others(26): Show |
29 | HG00639.hp2 HG00735.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.4592+1105_4592+110 others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 93010410 | ||||||
| chr15:93010462 | A | G | 142 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(139): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4592+1139A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010462 | |||||||
| chr15:93010693 | G | C | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4592+1370G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010693 | |||||||
| chr15:93010715 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(14): Show |
18 | HG01123.hp2 HG01192.hp1 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.4592+1392C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010715 | |||||||
| chr15:93010868 | C | T | 4 | a0001c0002t0002g0231 a0001c0002t0005g0229 a0001c0002t0005g0230 others(1): Show |
4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4593-1477C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010868 | |||||||
| chr15:93010956 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.4593-1389T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010956 | |||||||
| chr15:93010990 | G | A | 1 | a0001c0004t0004g0285 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4593-1355G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93010990 | |||||||
| chr15:93011071 | G | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4593-1274G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011071 | |||||||
| chr15:93011073 | C | CT | 6 | a0001c0001t0001g0007 a0001c0001t0006g0269 a0001c0009t0002g0044 others(3): Show |
6 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.4593-1260dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | INFO_REALIGN_3_PRIME | chr15 | 93011073 | ||||||
| chr15:93011108 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4593-1237A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011108 | |||||||
| chr15:93011329 | A | G | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4593-1016A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011329 | |||||||
| chr15:93011473 | A | G | 15 | a0001c0001t0008g0217 a0001c0001t0008g0218 a0001c0001t0008g0219 others(12): Show |
15 | HG00323.hp2 HG00741.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.4593-872A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011473 | |||||||
| chr15:93011585 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0122 |
2 | HG02602.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.4593-760G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011585 | |||||||
| chr15:93011723 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0211 |
2 | NA19007.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.4593-622G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011723 | |||||||
| chr15:93011878 | A | G | 4 | a0001c0002t0002g0231 a0001c0002t0005g0229 a0001c0002t0005g0230 others(1): Show |
4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4593-467A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011878 | |||||||
| chr15:93011969 | G | A | 225 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.4593-376G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93011969 | |||||||
| chr15:93012020 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.4593-325A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93012020 | |||||||
| chr15:93012141 | C | G | 1 | a0001c0003t0003g0128 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4593-204C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93012141 | |||||||
| chr15:93012199 | A | G | 1 | a0001c0003t0001g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.4593-146A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93012199 | |||||||
| chr15:93012233 | A | G | 2 | a0001c0001t0008g0040 a0001c0002t0002g0156 |
2 | HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4593-112A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93012233 | |||||||
| chr15:93012311 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG01258.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4593-34A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 35/38 | chr15 | 93012311 | |||||||
| chr15:93012487 | A | G | 43 | a0001c0001t0001g0016 a0001c0001t0020g0113 a0001c0002t0001g0234 others(40): Show |
43 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.4692+43A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93012487 | |||||||
| chr15:93012504 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4692+60C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93012504 | |||||||
| chr15:93012643 | T | A | 4 | a0001c0002t0005g0220 a0001c0003t0005g0124 a0001c0003t0005g0166 others(1): Show |
4 | HG02809.hp2 HG02922.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4692+199T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93012643 | |||||||
| chr15:93012695 | C | A | 4 | a0001c0002t0002g0231 a0001c0002t0005g0229 a0001c0002t0005g0230 others(1): Show |
4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4692+251C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93012695 | |||||||
| chr15:93012800 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4692+356T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93012800 | |||||||
| chr15:93013088 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4692+644G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013088 | |||||||
| chr15:93013161 | C | T | 2 | a0001c0001t0008g0040 a0001c0002t0002g0156 |
2 | HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4692+717C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013161 | |||||||
| chr15:93013212 | G | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.4692+768G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013212 | |||||||
| chr15:93013302 | TCCGGAAA others(2): Show |
T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0028 others(76): Show |
80 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.4692+861_4692+869d others(11): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013302 | ||||||
| chr15:93013662 | C | T | 4 | a0001c0002t0002g0231 a0001c0002t0005g0229 a0001c0002t0005g0230 others(1): Show |
4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4693-1034C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013662 | |||||||
| chr15:93013725 | G | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4693-971G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013725 | |||||||
| chr15:93013736 | A | G | 3 | a0001c0003t0003g0161 a0001c0003t0005g0160 a0001c0007t0003g0157 |
3 | HG01884.hp1 HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4693-960A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013736 | |||||||
| chr15:93013746 | C | G | 39 | a0001c0001t0020g0113 a0001c0002t0001g0234 a0001c0002t0001g0235 others(36): Show |
39 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.4693-950C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013746 | |||||||
| chr15:93013832 | G | A | 1 | a0001c0002t0001g0236 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.4693-864G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93013832 | |||||||
| chr15:93013928 | C | CA | 17 | a0001c0001t0001g0188 a0001c0001t0006g0268 a0001c0001t0006g0269 others(14): Show |
17 | HG01109.hp2 HG01257.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.4693-740dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | ||||||
| chr15:93013928 | CA | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(128): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.4693-740delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | ||||||
| chr15:93013928 | CAA | C | 64 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(61): Show |
65 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.4693-741_4693-740d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | ||||||
| chr15:93013928 | CAAA | C | 9 | a0001c0002t0001g0239 a0001c0002t0002g0045 a0001c0002t0002g0046 others(6): Show |
9 | HG02280.hp2 HG02572.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.4693-742_4693-740d others(5): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | ||||||
| chr15:93013928 | CAAAAAA | C | 12 | a0001c0001t0001g0143 a0001c0002t0001g0091 a0001c0002t0001g0286 others(9): Show |
13 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.4693-745_4693-740d others(8): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | ||||||
| chr15:93013928 | CAAAAAAA others(9): Show |
C | 5 | a0001c0001t0001g0007 a0001c0009t0002g0044 a0001c0009t0002g0048 others(2): Show |
5 | HG00642.hp1 HG00673.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.4693-755_4693-740d others(18): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | INFO_REALIGN_3_PRIME | chr15 | 93013928 | ||||||
| chr15:93014098 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4693-598A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93014098 | |||||||
| chr15:93014235 | A | T | 1 | a0001c0003t0008g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4693-461A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93014235 | |||||||
| chr15:93014518 | C | T | 11 | a0001c0001t0008g0217 a0001c0001t0008g0218 a0001c0001t0008g0219 others(8): Show |
11 | HG00323.hp2 HG00741.hp2 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.4693-178C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 36/38 | chr15 | 93014518 | |||||||
| chr15:93014950 | A | G | 4 | a0001c0002t0002g0231 a0001c0002t0005g0229 a0001c0002t0005g0230 others(1): Show |
4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4906+41A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93014950 | |||||||
| chr15:93014970 | T | C | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4906+61T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93014970 | |||||||
| chr15:93015096 | T | G | 2 | a0001c0002t0011g0256 a0001c0002t0011g0257 |
2 | NA19000.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.4906+187T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015096 | |||||||
| chr15:93015188 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0199 |
2 | HG02083.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.4906+279C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015188 | |||||||
| chr15:93015400 | T | C | 1 | a0001c0001t0003g0274 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4906+491T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015400 | |||||||
| chr15:93015505 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4906+596G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015505 | |||||||
| chr15:93015531 | TAACTG | T | 12 | a0001c0001t0001g0143 a0001c0002t0001g0091 a0001c0002t0001g0286 others(9): Show |
13 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.4906+625_4906+629d others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93015531 | ||||||
| chr15:93015570 | A | ACAGTTTA others(25): Show |
13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4906+663_4906+694d others(34): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93015570 | ||||||
| chr15:93015754 | A | G | 2 | a0001c0001t0008g0040 a0001c0002t0002g0156 |
2 | HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4906+845A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015754 | |||||||
| chr15:93015839 | A | C | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4906+930A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015839 | |||||||
| chr15:93015849 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4906+940C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015849 | |||||||
| chr15:93015948 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.4906+1039A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93015948 | |||||||
| chr15:93016074 | T | G | 17 | a0001c0001t0001g0143 a0001c0001t0003g0274 a0001c0002t0001g0091 others(14): Show |
18 | HG00099.hp2 HG00642.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.4906+1165T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016074 | |||||||
| chr15:93016093 | T | TA | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4906+1185dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016093 | ||||||
| chr15:93016105 | C | T | 5 | a0001c0004t0007g0013 a0001c0004t0007g0014 a0001c0004t0007g0017 others(2): Show |
5 | HG00639.hp1 HG01433.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.4906+1196C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016105 | |||||||
| chr15:93016123 | G | A | 33 | a0001c0001t0001g0143 a0001c0001t0001g0259 a0001c0001t0006g0253 others(30): Show |
34 | HG00099.hp2 HG00642.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.4906+1214G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016123 | |||||||
| chr15:93016156 | T | C | 1 | a0001c0004t0004g0092 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4906+1247T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016156 | |||||||
| chr15:93016157 | C | T | 50 | a0001c0001t0001g0143 a0001c0002t0001g0091 a0001c0002t0001g0234 others(47): Show |
51 | HG00099.hp2 HG00423.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.4906+1248C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016157 | |||||||
| chr15:93016265 | A | G | 1 | a0001c0005t0007g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4906+1356A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016265 | |||||||
| chr15:93016285 | C | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4906+1376C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016285 | |||||||
| chr15:93016285 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.4906+1376C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016285 | |||||||
| chr15:93016381 | A | G | 40 | a0001c0001t0001g0016 a0001c0002t0001g0234 a0001c0002t0001g0235 others(37): Show |
40 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.4906+1472A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016381 | |||||||
| chr15:93016383 | G | A | 4 | a0001c0002t0002g0231 a0001c0002t0005g0229 a0001c0002t0005g0230 others(1): Show |
4 | HG02257.hp2 HG02572.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4906+1474G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016383 | |||||||
| chr15:93016489 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0001g0272 others(1): Show |
5 | HG01123.hp2 HG02683.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.4906+1580G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016489 | |||||||
| chr15:93016519 | T | A | 1 | a0001c0009t0002g0048 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4906+1610T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016519 | |||||||
| chr15:93016539 | T | C | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4906+1630T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016539 | |||||||
| chr15:93016747 | G | A | 1 | a0001c0015t0005g0288 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4906+1838G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016747 | |||||||
| chr15:93016779 | C | CAAAAAAA others(2): Show |
26 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(23): Show |
26 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.4906+1877_4906+188 others(13): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | ||||||
| chr15:93016779 | C | CAAAAAAA others(3): Show |
62 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0068 others(59): Show |
63 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.4906+1876_4906+188 others(14): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | ||||||
| chr15:93016779 | C | CAAAAAAA others(4): Show |
137 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0028 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.4906+1875_4906+188 others(15): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | ||||||
| chr15:93016779 | C | CAAAAAAA others(5): Show |
16 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0032 others(13): Show |
17 | HG00673.hp1 HG00735.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.4906+1874_4906+188 others(16): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | ||||||
| chr15:93016779 | C | CAAAAAAA others(6): Show |
4 | a0001c0001t0001g0200 a0001c0002t0002g0045 a0001c0002t0002g0046 others(1): Show |
4 | HG03453.hp2 HG04115.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4906+1873_4906+188 others(17): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | ||||||
| chr15:93016779 | CA | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(10): Show |
14 | HG01123.hp2 HG01192.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.4906+1885delA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93016779 | ||||||
| chr15:93016799 | A | G | 1 | a0001c0002t0002g0156 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4906+1890A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016799 | |||||||
| chr15:93016814 | C | T | 2 | a0001c0010t0002g0182 a0001c0010t0002g0222 |
2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.4906+1905C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016814 | |||||||
| chr15:93016862 | A | G | 1 | a0001c0002t0001g0249 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4906+1953A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016862 | |||||||
| chr15:93016865 | A | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0199 |
2 | HG02083.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.4906+1956A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93016865 | |||||||
| chr15:93017057 | G | A | 1 | a0001c0001t0011g0176 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.4906+2148G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017057 | |||||||
| chr15:93017101 | G | T | 45 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(42): Show |
46 | HG00323.hp2 HG00642.hp1 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.4906+2192G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017101 | |||||||
| chr15:93017327 | C | CT | 216 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(213): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.4906+2421dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93017327 | ||||||
| chr15:93017331 | C | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.4906+2422C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017331 | |||||||
| chr15:93017492 | A | AT | 34 | a0001c0001t0001g0033 a0001c0001t0001g0056 a0001c0001t0001g0057 others(31): Show |
34 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.4907-2493dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93017492 | ||||||
| chr15:93017492 | A | ATTT | 10 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(7): Show |
10 | HG01074.hp2 HG01099.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.4907-2495_4907-249 others(7): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93017492 | ||||||
| chr15:93017492 | AT | A | 32 | a0001c0001t0001g0027 a0001c0001t0003g0274 a0001c0001t0008g0040 others(29): Show |
32 | HG00323.hp2 HG00735.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.4907-2493delT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93017492 | ||||||
| chr15:93017492 | ATT | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(54): Show |
58 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.4907-2494_4907-249 others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93017492 | ||||||
| chr15:93017571 | T | C | 38 | a0001c0002t0001g0234 a0001c0002t0001g0235 a0001c0002t0001g0236 others(35): Show |
38 | HG00423.hp2 HG00558.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.4907-2441T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017571 | |||||||
| chr15:93017620 | A | T | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.4907-2392A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017620 | |||||||
| chr15:93017829 | G | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 |
3 | HG01433.hp1 HG02735.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.4907-2183G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017829 | |||||||
| chr15:93017962 | A | T | 5 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0005g0224 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4907-2050A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93017962 | |||||||
| chr15:93018187 | T | C | 1 | a0001c0002t0002g0181 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4907-1825T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018187 | |||||||
| chr15:93018259 | T | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0069 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4907-1753T>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018259 | |||||||
| chr15:93018305 | G | A | 5 | a0001c0002t0002g0181 a0001c0002t0002g0223 a0001c0002t0005g0224 others(2): Show |
5 | HG02572.hp2 HG02630.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4907-1707G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018305 | |||||||
| chr15:93018370 | T | G | 2 | a0001c0001t0008g0040 a0001c0002t0002g0156 |
2 | HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4907-1642T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018370 | |||||||
| chr15:93018412 | G | T | 55 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0026 others(52): Show |
57 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.4907-1600G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018412 | |||||||
| chr15:93018415 | A | G | 2 | a0001c0009t0002g0044 a0001c0009t0012g0043 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4907-1597A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018415 | |||||||
| chr15:93018667 | C | T | 1 | a0001c0006t0004g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.4907-1345C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018667 | |||||||
| chr15:93018683 | C | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0037 others(10): Show |
14 | HG01123.hp2 HG01192.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.4907-1329C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018683 | |||||||
| chr15:93018713 | C | G | 218 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(215): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.4907-1299C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018713 | |||||||
| chr15:93018736 | C | G | 22 | a0001c0001t0001g0016 a0001c0002t0001g0234 a0001c0002t0008g0012 others(19): Show |
22 | HG00639.hp1 HG00642.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.4907-1276C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018736 | |||||||
| chr15:93018767 | A | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4907-1245A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018767 | |||||||
| chr15:93018770 | C | G | 1 | a0001c0002t0001g0246 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4907-1242C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93018770 | |||||||
| chr15:93019090 | A | T | 1 | a0001c0002t0001g0252 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4907-922A>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019090 | |||||||
| chr15:93019135 | T | C | 2 | a0001c0002t0003g0227 a0001c0002t0005g0228 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.4907-877T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019135 | |||||||
| chr15:93019293 | T | C | 21 | a0001c0001t0001g0281 a0001c0001t0002g0278 a0001c0001t0002g0293 others(18): Show |
21 | HG00544.hp1 HG00639.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.4907-719T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019293 | |||||||
| chr15:93019306 | G | A | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4907-706G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019306 | |||||||
| chr15:93019334 | T | G | 13 | a0001c0001t0001g0259 a0001c0001t0006g0253 a0001c0001t0006g0260 others(10): Show |
13 | HG00735.hp2 HG01074.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.4907-678T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019334 | |||||||
| chr15:93019390 | C | T | 1 | a0001c0005t0004g0154 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4907-622C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019390 | |||||||
| chr15:93019433 | G | A | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-579G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019433 | |||||||
| chr15:93019435 | C | A | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-577C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019435 | |||||||
| chr15:93019436 | T | C | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-576T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019436 | |||||||
| chr15:93019439 | A | G | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-573A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019439 | |||||||
| chr15:93019441 | A | C | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-571A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019441 | |||||||
| chr15:93019442 | T | G | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-570T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019442 | |||||||
| chr15:93019444 | T | G | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-568T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019444 | |||||||
| chr15:93019446 | G | T | 1 | a0001c0001t0009g0011 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.4907-566G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019446 | |||||||
| chr15:93019527 | T | C | 2 | a0001c0002t0002g0156 a0001c0003t0002g0169 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4907-485T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019527 | |||||||
| chr15:93019607 | A | C | 4 | a0001c0001t0003g0274 a0001c0002t0005g0224 a0001c0002t0005g0225 others(1): Show |
4 | HG03041.hp1 HG03209.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.4907-405A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019607 | |||||||
| chr15:93019676 | G | A | 1 | a0001c0001t0005g0179 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4907-336G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019676 | |||||||
| chr15:93019683 | C | T | 1 | a0001c0004t0010g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4907-329C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019683 | |||||||
| chr15:93019708 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG03492.hp2 HG03710.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4907-304C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019708 | |||||||
| chr15:93019743 | A | G | 7 | a0001c0001t0001g0053 a0001c0001t0009g0009 a0001c0001t0009g0010 others(4): Show |
7 | HG00544.hp2 HG01192.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.4907-269A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019743 | |||||||
| chr15:93019825 | T | C | 1 | a0001c0010t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4907-187T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | chr15 | 93019825 | |||||||
| chr15:93019934 | C | CA | 34 | a0001c0001t0001g0006 a0001c0001t0001g0072 a0001c0001t0001g0197 others(31): Show |
35 | HG00558.hp2 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.4907-65dupA | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93019934 | ||||||
| chr15:93019934 | C | CAA | 26 | a0001c0001t0001g0086 a0001c0001t0001g0201 a0001c0001t0002g0293 others(23): Show |
27 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.4907-66_4907-65dup others(2): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 37/38 | INFO_REALIGN_3_PRIME | chr15 | 93019934 | ||||||
| chr15:93020325 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.5153+67A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020325 | |||||||
| chr15:93020366 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.5153+108C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020366 | |||||||
| chr15:93020382 | C | G | 1 | a0001c0002t0009g0022 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5153+124C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020382 | |||||||
| chr15:93020399 | A | G | 1 | a0001c0003t0003g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.5153+141A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020399 | |||||||
| chr15:93020431 | G | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(250): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.5153+173G>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020431 | |||||||
| chr15:93020556 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.5153+298G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020556 | |||||||
| chr15:93020677 | A | G | 27 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0086 others(24): Show |
27 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.5153+419A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020677 | |||||||
| chr15:93020793 | A | G | 15 | a0001c0001t0001g0193 a0001c0001t0006g0080 a0001c0001t0006g0084 others(12): Show |
15 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.5153+535A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020793 | |||||||
| chr15:93020815 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.5153+557T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020815 | |||||||
| chr15:93020987 | G | A | 1 | a0001c0001t0002g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5153+729G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93020987 | |||||||
| chr15:93021271 | CATCCTT | C | 9 | a0001c0001t0002g0008 a0001c0001t0002g0278 a0001c0001t0002g0295 others(6): Show |
9 | HG01069.hp2 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.5153+1017_5153+102 others(10): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93021271 | ||||||
| chr15:93021538 | T | C | 85 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0065 others(82): Show |
86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.5153+1280T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021538 | |||||||
| chr15:93021697 | A | C | 1 | a0001c0006t0004g0158 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5153+1439A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021697 | |||||||
| chr15:93021742 | T | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
187 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.5153+1484T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021742 | |||||||
| chr15:93021854 | G | A | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5153+1596G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021854 | |||||||
| chr15:93021860 | T | C | 14 | a0001c0001t0006g0080 a0001c0001t0006g0084 a0001c0001t0006g0253 others(11): Show |
14 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.5153+1602T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021860 | |||||||
| chr15:93021936 | A | C | 1 | a0001c0001t0001g0191 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.5153+1678A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021936 | |||||||
| chr15:93021942 | C | A | 1 | a0001c0010t0002g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5153+1684C>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93021942 | |||||||
| chr15:93022149 | A | G | 3 | a0001c0002t0002g0045 a0001c0002t0002g0046 a0001c0002t0002g0232 |
3 | HG03453.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.5153+1891A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022149 | |||||||
| chr15:93022260 | C | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
177 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.5153+2002C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022260 | |||||||
| chr15:93022260 | C | T | 2 | a0001c0003t0003g0149 a0001c0003t0003g0290 |
2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.5153+2002C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022260 | |||||||
| chr15:93022339 | G | A | 17 | a0001c0001t0001g0016 a0001c0004t0007g0013 a0001c0004t0007g0014 others(14): Show |
17 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.5154-2033G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022339 | |||||||
| chr15:93022499 | G | A | 3 | a0001c0001t0002g0278 a0001c0001t0002g0295 a0001c0003t0002g0125 |
3 | HG01069.hp2 HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.5154-1873G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022499 | |||||||
| chr15:93022520 | G | A | 1 | a0001c0013t0019g0168 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.5154-1852G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022520 | |||||||
| chr15:93022601 | C | G | 4 | a0001c0002t0001g0235 a0001c0002t0001g0247 a0001c0002t0001g0248 others(1): Show |
4 | NA18967.hp1 NA18978.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.5154-1771C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022601 | |||||||
| chr15:93022830 | A | C | 9 | a0001c0001t0008g0040 a0001c0001t0008g0217 a0001c0001t0008g0218 others(6): Show |
9 | HG00741.hp1 HG01070.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.5154-1542A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022830 | |||||||
| chr15:93022915 | G | A | 275 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(272): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.5154-1457G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022915 | |||||||
| chr15:93022924 | C | T | 12 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(9): Show |
12 | HG00323.hp1 HG00735.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.5154-1448C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93022924 | |||||||
| chr15:93023009 | C | T | 1 | a0001c0003t0014g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.5154-1363C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023009 | |||||||
| chr15:93023034 | T | C | 9 | a0001c0001t0008g0040 a0001c0001t0008g0217 a0001c0001t0008g0218 others(6): Show |
9 | HG00741.hp1 HG01070.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.5154-1338T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023034 | |||||||
| chr15:93023075 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5154-1297A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023075 | |||||||
| chr15:93023136 | T | C | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5154-1236T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023136 | |||||||
| chr15:93023181 | A | C | 23 | a0001c0001t0001g0029 a0001c0002t0001g0091 a0001c0003t0012g0126 others(20): Show |
24 | HG00140.hp2 HG00738.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.5154-1191A>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023181 | |||||||
| chr15:93023193 | C | G | 12 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0039 others(9): Show |
12 | HG00323.hp1 HG00735.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.5154-1179C>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023193 | |||||||
| chr15:93023247 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5154-1125C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023247 | |||||||
| chr15:93023452 | G | A | 203 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(200): Show |
206 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.5154-920G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023452 | |||||||
| chr15:93023573 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.5154-799A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023573 | |||||||
| chr15:93023604 | A | G | 1 | a0001c0005t0004g0287 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.5154-768A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023604 | |||||||
| chr15:93023668 | G | GTT | 8 | a0001c0001t0008g0040 a0001c0001t0008g0217 a0001c0001t0008g0218 others(5): Show |
8 | HG00741.hp1 HG01070.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.5154-695_5154-694d others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93023668 | ||||||
| chr15:93023677 | T | G | 2 | a0001c0002t0003g0227 a0001c0003t0003g0152 |
2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5154-695T>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023677 | |||||||
| chr15:93023679 | G | GT | 34 | a0001c0001t0002g0008 a0001c0001t0002g0085 a0001c0001t0002g0278 others(31): Show |
34 | HG00099.hp2 HG00544.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.5154-692dupT | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93023679 | ||||||
| chr15:93023679 | G | GTT | 23 | a0001c0002t0001g0091 a0001c0003t0012g0126 a0001c0003t0012g0131 others(20): Show |
24 | HG00140.hp2 HG00738.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.5154-692_5154-691i others(4): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93023679 | ||||||
| chr15:93023681 | G | T | 58 | a0001c0001t0002g0008 a0001c0001t0002g0085 a0001c0001t0002g0278 others(55): Show |
59 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.5154-691G>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023681 | |||||||
| chr15:93023822 | A | G | 1 | a0001c0004t0004g0284 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.5154-550A>G | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93023822 | |||||||
| chr15:93023922 | T | TCCAAGCT others(312): Show |
7 | a0001c0005t0004g0153 a0001c0005t0004g0154 a0001c0005t0004g0287 others(4): Show |
7 | HG00738.hp2 HG01081.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.5154-434_5154-433i others(321): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93023922 | ||||||
| chr15:93023922 | T | TCCAAGCT others(313): Show |
1 | a0001c0005t0004g0283 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5154-434_5154-433i others(322): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93023922 | ||||||
| chr15:93024122 | G | A | 92 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0028 others(89): Show |
92 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.5154-250G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024122 | |||||||
| chr15:93024137 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.5154-235C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024137 | |||||||
| chr15:93024150 | T | C | 1 | a0001c0007t0007g0030 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5154-222T>C | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024150 | |||||||
| chr15:93024158 | T | TGTAC | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
168 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.5154-213_5154-210d others(6): Show |
CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | INFO_REALIGN_3_PRIME | chr15 | 93024158 | ||||||
| chr15:93024296 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
169 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.5154-76G>A | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024296 | |||||||
| chr15:93024297 | C | T | 11 | a0001c0004t0007g0013 a0001c0004t0007g0014 a0001c0004t0007g0017 others(8): Show |
11 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.5154-75C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024297 | |||||||
| chr15:93024298 | C | T | 11 | a0001c0004t0007g0013 a0001c0004t0007g0014 a0001c0004t0007g0017 others(8): Show |
11 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.5154-74C>T | CHD2 | ENSG00000173575.24 | transcript | ENST00000394196.9 | protein_coding | 38/38 | chr15 | 93024298 |