Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 66005 |
| ensemblid | ENSG00000177830.18 |
| hgncid | 28474 |
| symbol | CHID1 |
| name | chitinase domain containing 1 |
| refseq_nuc | NM_023947.4 |
| refseq_prot | NP_076436.3 |
| ensembl_nuc | ENST00000323578.13 |
| ensembl_prot | ENSP00000325055.8 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 867859 |
| end | 910810 |
| strand | - |
| ver | v1.2 |
| region | chr11:867859-910810 |
| region5000 | chr11:862859-915810 |
| regionname0 | CHID1_chr11_867859_910810 |
| regionname5000 | CHID1_chr11_862859_915810 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 393 | 213 | 43 | 24 | 109 | 7 | 30 | 76 | CHID1_chr11_862859_915810 | CHID1 | MRTLF others(388): Show |
chr11 | 862859 | 915810 |
| a0002 | 1/0 | 393 | 160 | 43 | 42 | 57 | 7 | 10 | 44 | CHID1_chr11_862859_915810 | CHID1 | MRTLF others(388): Show |
chr11 | 862859 | 915810 |
| a0003 | 0/1 | 393 | 10 | 0 | 7 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | MRTLF others(388): Show |
chr11 | 862859 | 915810 |
| a0004 | 0/0 | 393 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | MRTLF others(388): Show |
chr11 | 862859 | 915810 |
| a0005 | 0/0 | 393 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | MRTLF others(388): Show |
chr11 | 862859 | 915810 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1179 | 212 | 42 | 24 | 109 | 7 | 30 | CHID1_chr11_862859_915810 | CHID1 | ATGCG others(1174): Show |
chr11 | 862859 | 915810 | ||
| a0001c0008 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | ATGCG others(1174): Show |
chr11 | 862859 | 915810 | ||
| a0002c0002 | 1/0 | 1179 | 157 | 40 | 42 | 57 | 7 | 10 | CHID1_chr11_862859_915810 | CHID1 | ATGCG others(1174): Show |
chr11 | 862859 | 915810 | ||
| a0002c0005 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | ATGCG others(1174): Show |
chr11 | 862859 | 915810 | ||
| a0002c0006 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | ATGCG others(1174): Show |
chr11 | 862859 | 915810 | ||
| a0002c0007 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | ATGCG others(1174): Show |
chr11 | 862859 | 915810 | ||
| a0003c0003 | 0/1 | 1179 | 10 | 0 | 7 | 0 | 2 | 0 | CHID1_chr11_862859_915810 | CHID1 | ATGCG others(1174): Show |
chr11 | 862859 | 915810 | ||
| a0004c0004 | 0/0 | 1179 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | ATGCG others(1174): Show |
chr11 | 862859 | 915810 | ||
| a0005c0009 | 0/0 | 1179 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | ATGCG others(1174): Show |
chr11 | 862859 | 915810 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3260 | 170 | 32 | 20 | 93 | 4 | 21 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0002 | 0/0 | 3260 | 23 | 3 | 3 | 11 | 2 | 4 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0003 | 0/0 | 3260 | 3 | 3 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0004 | 0/0 | 3260 | 2 | 1 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0007 | 0/0 | 3260 | 2 | 0 | 0 | 0 | 1 | 1 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0009 | 0/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0013 | 0/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0016 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0017 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0019 | 0/0 | 3235 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3230): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0021 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0022 | 0/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0023 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0028 | 0/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0029 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0030 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0001t0031 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0001c0008t0001 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0001 | 0/0 | 3260 | 143 | 33 | 42 | 52 | 7 | 9 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0002 | 0/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0005 | 0/0 | 3260 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0008 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0010 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0011 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0012 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0014 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0015 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0018 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0020 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0024 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0026 | 1/0 | 3260 | 1 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0002t0027 | 0/0 | 3260 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0005t0025 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0006t0006 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0002c0007t0006 | 0/0 | 3260 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0003c0003t0001 | 0/0 | 3260 | 3 | 0 | 2 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0003c0003t0002 | 0/1 | 3260 | 7 | 0 | 5 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0004c0004t0001 | 0/0 | 3260 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| a0005c0009t0001 | 0/0 | 3260 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | GTGCG others(3255): Show |
chr11 | 862859 | 915810 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 3 | 1 | 0 | 2 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0009g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0013g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0016g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0019g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0021g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0022g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0023g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0028g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0029g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0030g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0001t0031g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0001c0008t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0001 | 0/0 | 9 | 0 | 4 | 5 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0006 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0008g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0010g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0011g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0014g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0015g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0018g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0020g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0024g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0026g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0002t0027g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0005t0025g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0006t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0002c0007t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0003c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0003c0003t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0003c0003t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0003c0003t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0003c0003t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0003c0003t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0003c0003t0002g0160 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0003c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0004c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0004c0004t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| a0005c0009t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0153 | EUR | GBR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0215 | EUR | GBR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0245 | EUR | FIN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0013 | EUR | FIN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0013 | EUR | FIN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0006 | EUR | FIN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00438 | hp2 | a0001 | c0001 | t0023 | g0151 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00558 | hp2 | a0002 | c0002 | t0005 | g0261 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0250 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0272 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00733 | hp2 | a0003 | c0003 | t0002 | g0099 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0308 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0279 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0288 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0275 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01070 | hp2 | a0003 | c0003 | t0002 | g0158 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01071 | hp1 | a0003 | c0003 | t0002 | g0159 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01106 | hp1 | a0003 | c0003 | t0002 | g0154 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0282 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01109 | hp1 | a0003 | c0003 | t0002 | g0039 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0091 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0152 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0243 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0060 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01243 | hp2 | a0005 | c0009 | t0001 | g0090 | AMR | PUR | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0312 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0285 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0286 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0259 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0084 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0304 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0258 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0287 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0248 | AMR | CLM | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0274 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01516 | hp1 | a0003 | c0003 | t0002 | g0161 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0157 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01884 | hp2 | a0002 | c0002 | t0020 | g0088 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0253 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0315 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0281 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0311 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02040 | hp2 | a0002 | c0002 | t0015 | g0085 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02071 | hp2 | a0002 | c0002 | t0008 | g0194 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02129 | hp2 | a0001 | c0001 | t0031 | g0320 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02145 | hp2 | a0002 | c0002 | t0024 | g0268 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CDX | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | CDX | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CDX | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0271 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02258 | hp2 | a0002 | c0002 | t0012 | g0050 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0242 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0033 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0186 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02572 | hp1 | a0002 | c0002 | t0014 | g0071 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02615 | hp2 | a0001 | c0001 | t0019 | g0051 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02630 | hp2 | a0001 | c0008 | t0001 | g0138 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02683 | hp1 | a0001 | c0001 | t0022 | g0176 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02738 | hp1 | a0001 | c0001 | t0028 | g0184 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0307 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0314 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0081 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02965 | hp1 | a0002 | c0002 | t0010 | g0236 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0297 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02976 | hp2 | a0004 | c0004 | t0001 | g0309 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0247 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0218 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03130 | hp2 | a0002 | c0005 | t0025 | g0237 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03139 | hp2 | a0002 | c0007 | t0006 | g0126 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0075 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03225 | hp2 | a0002 | c0002 | t0018 | g0052 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03486 | hp1 | a0001 | c0001 | t0016 | g0083 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0198 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03579 | hp1 | a0002 | c0002 | t0011 | g0296 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0086 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0122 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0260 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0246 | SAS | PJL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0209 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0273 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG04184 | hp2 | a0001 | c0001 | t0009 | g0255 | SAS | BEB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG04199 | hp1 | a0001 | c0001 | t0013 | g0044 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0155 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | CHB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | CHB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0284 | EAS | CHB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0270 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18952 | hp2 | a0002 | c0002 | t0027 | g0257 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18957 | hp1 | a0001 | c0001 | t0021 | g0106 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18965 | hp2 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18971 | hp1 | a0001 | c0001 | t0030 | g0321 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19043 | hp2 | a0002 | c0006 | t0006 | g0125 | AFR | LWK | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19057 | hp2 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19064 | hp1 | a0002 | c0002 | t0005 | g0293 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19074 | hp2 | a0001 | c0001 | t0029 | g0187 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0067 | AFR | YRI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | ASW | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0306 | EUR | TSI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0013 | EUR | TSI | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | GIH | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0283 | SAS | GIH | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0226 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0082 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0225 | AFR | MSL | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0269 | AFR | USA | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | USA | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | USA | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | USA | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | LWK | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| NA21309 | hp2 | a0004 | c0004 | t0001 | g0041 | AFR | LWK | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0002 | g0160 | REF | REF | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0026 | g0241 | REF | REF | CHID1_chr11_862859_915810 | CHID1 | chr11 | 862859 | 915810 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:870446 | G | A | 3 | a0001 a0003 a0004 |
224 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(221): Show |
missense_variant | MODERATE | c.1013C>T | p.Ala338Val | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/13 | 1092/3260 | 1013/1182 | 338/393 | chr11 | 870446 | |||
| chr11:870467 | C | T | 1 | a0003 | 9 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(6): Show |
missense_variant | MODERATE | c.992G>A | p.Arg331Gln | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/13 | 1071/3260 | 992/1182 | 331/393 | chr11 | 870467 | |||
| chr11:903039 | G | A | 1 | a0004 | 2 | HG02976.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.184C>T | p.Leu62Phe | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/13 | 263/3260 | 184/1182 | 62/393 | chr11 | 903039 | |||
| chr11:903048 | T | C | 1 | a0005 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.175A>G | p.Ser59Gly | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/13 | 254/3260 | 175/1182 | 59/393 | chr11 | 903048 | |||
| chr11:904857 | G | A | 1 | a0001 | 1 | NA19074.hp2 | splice_region_variant | LOW | c.-41C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/13 | chr11 | 904857 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:870136 | G | A | 2 | a0002c0006 a0002c0007 |
2 | HG03139.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.1068C>T | p.Phe356Phe | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/13 | 1147/3260 | 1068/1182 | 356/393 | chr11 | 870136 | |||
| chr11:870486 | G | A | 1 | a0002c0007 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.973C>T | p.Leu325Leu | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/13 | 1052/3260 | 973/1182 | 325/393 | chr11 | 870486 | |||
| chr11:883264 | G | A | 1 | a0001c0008 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.843C>T | p.Cys281Cys | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/13 | 922/3260 | 843/1182 | 281/393 | chr11 | 883264 | |||
| chr11:903070 | C | G | 1 | a0002c0005 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.153G>C | p.Val51Val | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/13 | 232/3260 | 153/1182 | 51/393 | chr11 | 903070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:868139 | ACCACCCT others(18): Show |
A | 1 | a0001c0001t0019 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1694_*1718delGGGA others(21): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1694 | chr11 | 868139 | ||||||
| chr11:868226 | A | G | 1 | a0002c0002t0018 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1632T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1632 | chr11 | 868226 | ||||||
| chr11:868265 | C | A | 1 | a0002c0002t0020 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1593G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1593 | chr11 | 868265 | ||||||
| chr11:868303 | T | C | 1 | a0001c0001t0021 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1555A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1555 | chr11 | 868303 | ||||||
| chr11:868304 | C | G | 1 | a0002c0002t0005 | 2 | HG00558.hp2 NA19064.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1554G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1554 | chr11 | 868304 | ||||||
| chr11:868385 | T | G | 1 | a0001c0001t0023 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1473A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1473 | chr11 | 868385 | ||||||
| chr11:868402 | A | T | 1 | a0002c0005t0025 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1456T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1456 | chr11 | 868402 | ||||||
| chr11:868411 | A | C | 1 | a0001c0001t0004 | 2 | HG01243.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1447T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1447 | chr11 | 868411 | ||||||
| chr11:868419 | G | T | 1 | a0001c0001t0017 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1439C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1439 | chr11 | 868419 | ||||||
| chr11:868502 | G | A | 1 | a0001c0001t0022 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1356C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1356 | chr11 | 868502 | ||||||
| chr11:868533 | G | A | 1 | a0001c0001t0003 | 3 | HG02055.hp1 HG03209.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1325C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1325 | chr11 | 868533 | ||||||
| chr11:868654 | C | G | 1 | a0002c0002t0015 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1204G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1204 | chr11 | 868654 | ||||||
| chr11:868706 | C | T | 1 | a0001c0001t0016 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1152 | chr11 | 868706 | ||||||
| chr11:868727 | C | A | 2 | a0002c0006t0006 a0002c0007t0006 |
2 | HG03139.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1131G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1131 | chr11 | 868727 | ||||||
| chr11:868740 | C | T | 1 | a0002c0002t0015 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1118G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 1118 | chr11 | 868740 | ||||||
| chr11:868865 | G | A | 1 | a0001c0001t0023 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*993C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 993 | chr11 | 868865 | ||||||
| chr11:869119 | G | A | 1 | a0002c0002t0024 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*739C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 739 | chr11 | 869119 | ||||||
| chr11:869158 | C | T | 4 | a0001c0001t0002 a0001c0001t0029 a0002c0002t0002 others(1): Show |
31 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*700G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 700 | chr11 | 869158 | ||||||
| chr11:869159 | G | A | 1 | a0001c0001t0007 | 2 | HG00140.hp2 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*699C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 699 | chr11 | 869159 | ||||||
| chr11:869253 | C | G | 1 | a0002c0002t0014 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 605 | chr11 | 869253 | ||||||
| chr11:869280 | C | T | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
3_prime_UTR_variant | MODIFIER | c.*578G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 578 | chr11 | 869280 | ||||||
| chr11:869311 | C | T | 1 | a0001c0001t0013 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 547 | chr11 | 869311 | ||||||
| chr11:869315 | C | T | 1 | a0002c0002t0012 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*543G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 543 | chr11 | 869315 | ||||||
| chr11:869360 | C | T | 1 | a0002c0002t0011 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*498G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 498 | chr11 | 869360 | ||||||
| chr11:869424 | C | T | 1 | a0002c0002t0010 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*434G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 434 | chr11 | 869424 | ||||||
| chr11:869444 | G | C | 1 | a0001c0001t0031 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*414C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 414 | chr11 | 869444 | ||||||
| chr11:869471 | G | A | 1 | a0002c0002t0027 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 387 | chr11 | 869471 | ||||||
| chr11:869641 | G | C | 1 | a0001c0001t0028 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*217C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 217 | chr11 | 869641 | ||||||
| chr11:869724 | G | T | 1 | a0001c0001t0009 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 134 | chr11 | 869724 | ||||||
| chr11:869796 | C | T | 1 | a0002c0002t0008 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 13/13 | 62 | chr11 | 869796 | ||||||
| chr11:910797 | G | A | 2 | a0001c0001t0030 a0001c0001t0031 |
2 | HG02129.hp2 NA18971.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/13 | chr11 | 910797 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:869959 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02683.hp2 | splice_region_variant&intron_variant | LOW | c.1084-3C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 869959 | |||||||
| chr11:869977 | G | A | 1 | a0002c0002t0001g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1084-21C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 869977 | |||||||
| chr11:870001 | C | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0199 |
3 | HG02015.hp2 HG02080.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1084-45G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 870001 | |||||||
| chr11:870074 | C | T | 1 | a0002c0002t0001g0310 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1083+47G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 870074 | |||||||
| chr11:870094 | CG | C | 6 | a0001c0001t0001g0094 a0002c0002t0001g0015 a0002c0002t0001g0079 others(3): Show |
7 | HG00738.hp1 HG01192.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1083+26delC | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 870094 | |||||||
| chr11:870095 | G | A | 28 | a0001c0001t0001g0162 a0001c0001t0002g0019 a0001c0001t0002g0025 others(25): Show |
31 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1083+26C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 12/12 | chr11 | 870095 | |||||||
| chr11:870237 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1041-74G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/12 | chr11 | 870237 | |||||||
| chr11:870316 | G | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0100 |
3 | NA19004.hp2 NA19065.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1040+103C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/12 | chr11 | 870316 | |||||||
| chr11:870389 | A | G | 8 | a0002c0002t0001g0007 a0002c0002t0001g0074 a0002c0002t0001g0087 others(5): Show |
10 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1040+30T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/12 | chr11 | 870389 | |||||||
| chr11:870400 | C | T | 5 | a0001c0001t0001g0072 a0001c0001t0003g0017 a0001c0001t0003g0078 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1040+19G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/12 | chr11 | 870400 | |||||||
| chr11:870401 | G | A | 8 | a0002c0002t0001g0007 a0002c0002t0001g0074 a0002c0002t0001g0087 others(5): Show |
10 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.1040+18C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 11/12 | chr11 | 870401 | |||||||
| chr11:870524 | G | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(105): Show |
135 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.960-25C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870524 | |||||||
| chr11:870660 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.960-161G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870660 | |||||||
| chr11:870722 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.960-223C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870722 | |||||||
| chr11:870812 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.960-313G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870812 | |||||||
| chr11:870930 | G | T | 1 | a0001c0001t0001g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.960-431C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870930 | |||||||
| chr11:870966 | G | A | 1 | a0002c0002t0001g0208 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.960-467C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870966 | |||||||
| chr11:870989 | CT | C | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
363 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.960-491delA | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 870989 | |||||||
| chr11:871014 | GGAGTCTC others(1125): Show |
G | 1 | a0001c0001t0001g0168 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.960-1647_960-516de others(1): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871014 | |||||||
| chr11:871030 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0133 a0001c0001t0001g0140 others(4): Show |
11 | HG00735.hp1 HG00741.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.960-531C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871030 | |||||||
| chr11:871049 | C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960-550G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871049 | |||||||
| chr11:871092 | G | A | 1 | a0002c0002t0001g0245 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.960-593C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871092 | |||||||
| chr11:871183 | C | T | 1 | a0001c0001t0019g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.960-684G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871183 | |||||||
| chr11:871203 | A | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.960-704T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871203 | |||||||
| chr11:871227 | G | A | 316 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(313): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.960-728C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871227 | |||||||
| chr11:871238 | G | A | 316 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(313): Show |
381 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(378): Show |
intron_variant | MODIFIER | c.960-739C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871238 | |||||||
| chr11:871328 | G | A | 1 | a0002c0002t0001g0297 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.960-829C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871328 | |||||||
| chr11:871531 | A | AGAACACT others(39): Show |
301 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.960-1033_960-1032i others(48): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871531 | |||||||
| chr11:871531 | A | AGAACACT others(39): Show |
1 | a0002c0007t0006g0126 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.960-1033_960-1032i others(48): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871531 | |||||||
| chr11:871531 | A | AGAACACT others(39): Show |
15 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0042 others(12): Show |
17 | HG00741.hp1 HG01884.hp1 HG02004.hp2 others(14): Show |
intron_variant | MODIFIER | c.960-1033_960-1032i others(48): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871531 | |||||||
| chr11:871582 | C | A | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.960-1083G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871582 | |||||||
| chr11:871591 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.960-1092T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871591 | |||||||
| chr11:871689 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.960-1190A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871689 | |||||||
| chr11:871703 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.960-1204T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871703 | |||||||
| chr11:871742 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.960-1243G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871742 | |||||||
| chr11:871759 | C | T | 1 | a0002c0002t0001g0086 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.960-1260G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871759 | |||||||
| chr11:871826 | C | CGGT | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.960-1328_960-1327i others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 871826 | |||||||
| chr11:872059 | GGAGGCTG others(14): Show |
G | 1 | a0002c0002t0001g0303 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.960-1581_960-1561d others(23): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872059 | |||||||
| chr11:872108 | G | T | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.960-1609C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872108 | |||||||
| chr11:872135 | C | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0110 |
2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.960-1636G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872135 | |||||||
| chr11:872314 | C | T | 1 | a0002c0002t0001g0280 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.960-1815G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872314 | |||||||
| chr11:872408 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0023 others(9): Show |
19 | HG00621.hp1 NA18947.hp1 NA18948.hp2 others(16): Show |
intron_variant | MODIFIER | c.960-1909G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872408 | |||||||
| chr11:872459 | T | C | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.960-1960A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872459 | |||||||
| chr11:872529 | C | T | 82 | a0001c0001t0001g0192 a0001c0001t0009g0255 a0002c0002t0001g0001 others(79): Show |
100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.960-2030G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872529 | |||||||
| chr11:872808 | G | A | 10 | a0002c0002t0001g0007 a0002c0002t0001g0040 a0002c0002t0001g0074 others(7): Show |
12 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.960-2309C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872808 | |||||||
| chr11:872922 | C | T | 1 | a0004c0004t0001g0309 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.960-2423G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872922 | |||||||
| chr11:872992 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.960-2493C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 872992 | |||||||
| chr11:873223 | C | G | 1 | a0002c0002t0001g0087 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.960-2724G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873223 | |||||||
| chr11:873482 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.960-2983C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873482 | |||||||
| chr11:873556 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0003g0078 |
3 | HG02055.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.960-3057C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873556 | |||||||
| chr11:873593 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.960-3094C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873593 | |||||||
| chr11:873595 | C | T | 1 | a0001c0001t0002g0027 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.960-3096G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873595 | |||||||
| chr11:873711 | G | A | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.960-3212C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873711 | |||||||
| chr11:873716 | A | G | 1 | a0002c0002t0001g0256 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.960-3217T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873716 | |||||||
| chr11:873771 | C | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(213): Show |
264 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.960-3272G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873771 | |||||||
| chr11:873962 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.960-3463C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873962 | |||||||
| chr11:873980 | GGA | G | 11 | a0002c0002t0001g0007 a0002c0002t0001g0040 a0002c0002t0001g0074 others(8): Show |
13 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.960-3483_960-3482d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 873980 | |||||||
| chr11:874038 | T | G | 3 | a0001c0001t0019g0051 a0002c0002t0001g0198 a0002c0002t0010g0236 |
3 | HG02615.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.960-3539A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874038 | |||||||
| chr11:874160 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.960-3661G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874160 | |||||||
| chr11:874184 | G | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0146 a0001c0001t0023g0151 |
3 | HG00438.hp2 NA18612.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.960-3685C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874184 | |||||||
| chr11:874189 | T | C | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.960-3690A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874189 | |||||||
| chr11:874291 | A | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.960-3792T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874291 | |||||||
| chr11:874305 | T | C | 4 | a0002c0002t0001g0053 a0002c0002t0001g0066 a0002c0002t0001g0067 others(1): Show |
4 | HG02055.hp2 HG02559.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.960-3806A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874305 | |||||||
| chr11:874350 | C | A | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.960-3851G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874350 | |||||||
| chr11:874442 | G | A | 1 | a0002c0002t0001g0248 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.960-3943C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874442 | |||||||
| chr11:874499 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.960-4000C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874499 | |||||||
| chr11:874501 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(36): Show |
49 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.960-4002G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874501 | |||||||
| chr11:874776 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0012 others(35): Show |
48 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.960-4277C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874776 | |||||||
| chr11:874935 | C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960-4436G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874935 | |||||||
| chr11:874960 | C | T | 1 | a0002c0002t0001g0249 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.960-4461G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 874960 | |||||||
| chr11:875500 | C | A | 1 | a0001c0001t0019g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.960-5001G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875500 | |||||||
| chr11:875549 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960-5050C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875549 | |||||||
| chr11:875591 | C | G | 1 | a0002c0002t0001g0284 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.960-5092G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875591 | |||||||
| chr11:875619 | G | A | 2 | a0004c0004t0001g0041 a0004c0004t0001g0309 |
2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.960-5120C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875619 | |||||||
| chr11:875689 | C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960-5190G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875689 | |||||||
| chr11:875825 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.960-5326G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875825 | |||||||
| chr11:875834 | A | G | 1 | a0002c0002t0001g0291 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.960-5335T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875834 | |||||||
| chr11:875843 | C | G | 1 | a0002c0002t0001g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.960-5344G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875843 | |||||||
| chr11:875981 | G | A | 1 | a0002c0002t0008g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.960-5482C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 875981 | |||||||
| chr11:876028 | C | CG | 3 | a0001c0001t0002g0199 a0002c0002t0001g0213 a0002c0002t0001g0235 |
3 | HG02080.hp2 HG02257.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.960-5530dupC | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876028 | |||||||
| chr11:876148 | G | T | 1 | a0002c0002t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.960-5649C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876148 | |||||||
| chr11:876245 | C | T | 3 | a0002c0002t0001g0285 a0002c0002t0001g0286 a0002c0002t0002g0155 |
3 | HG01256.hp2 HG01258.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.960-5746G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876245 | |||||||
| chr11:876582 | C | A | 2 | a0002c0006t0006g0125 a0002c0007t0006g0126 |
2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.960-6083G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876582 | |||||||
| chr11:876624 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
240 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.960-6125A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876624 | |||||||
| chr11:876707 | C | T | 13 | a0002c0002t0001g0007 a0002c0002t0001g0040 a0002c0002t0001g0074 others(10): Show |
15 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.960-6208G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876707 | |||||||
| chr11:876715 | C | T | 1 | a0001c0001t0001g0021 | 2 | NA18959.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.960-6216G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876715 | |||||||
| chr11:876755 | T | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
240 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.960-6256A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 876755 | |||||||
| chr11:877394 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.959+5754G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877394 | |||||||
| chr11:877406 | C | T | 1 | a0003c0003t0002g0154 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.959+5742G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877406 | |||||||
| chr11:877560 | T | C | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.959+5588A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877560 | |||||||
| chr11:877596 | C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+5552G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877596 | |||||||
| chr11:877717 | T | TGGCACTG others(25): Show |
1 | a0001c0001t0001g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.959+5399_959+5430d others(34): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877717 | |||||||
| chr11:877717 | T | TGGCACTG others(57): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0002c0002t0001g0082 |
4 | HG02145.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+5367_959+5430d others(66): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877717 | |||||||
| chr11:877750 | G | A | 1 | a0002c0002t0001g0091 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.959+5398C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877750 | |||||||
| chr11:877783 | G | GCACTGTG others(25): Show |
26 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0002g0019 others(23): Show |
28 | HG00140.hp1 HG00544.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.959+5333_959+5364d others(34): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877783 | |||||||
| chr11:877783 | G | GCACTGTG others(57): Show |
7 | a0001c0001t0002g0027 a0001c0001t0002g0097 a0001c0001t0002g0172 others(4): Show |
8 | HG02015.hp2 HG02040.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.959+5364_959+5365i others(66): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877783 | |||||||
| chr11:877783 | G | GCACTGTG others(57): Show |
13 | a0002c0002t0001g0007 a0002c0002t0001g0040 a0002c0002t0001g0074 others(10): Show |
15 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.959+5364_959+5365i others(66): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877783 | |||||||
| chr11:877783 | G | GCACTGTG others(57): Show |
147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
184 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(181): Show |
intron_variant | MODIFIER | c.959+5364_959+5365i others(66): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877783 | |||||||
| chr11:877815 | A | ACACTGTG others(153): Show |
1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+5332_959+5333i others(162): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877815 | |||||||
| chr11:877847 | G | A | 120 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0192 others(117): Show |
142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.959+5301C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877847 | |||||||
| chr11:877869 | T | C | 1 | a0002c0002t0001g0291 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.959+5279A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877869 | |||||||
| chr11:877869 | T | TTAGAAGG others(25): Show |
120 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0192 others(117): Show |
142 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.959+5278_959+5279i others(34): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 877869 | |||||||
| chr11:878151 | C | T | 1 | a0002c0002t0001g0191 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.959+4997G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878151 | |||||||
| chr11:878226 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.959+4922G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878226 | |||||||
| chr11:878253 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0145 |
3 | HG01934.hp2 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.959+4895T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878253 | |||||||
| chr11:878301 | C | T | 1 | a0002c0002t0001g0258 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.959+4847G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878301 | |||||||
| chr11:878372 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0124 a0001c0001t0001g0137 others(1): Show |
7 | HG02280.hp1 HG02630.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+4776G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878372 | |||||||
| chr11:878427 | G | A | 1 | a0002c0002t0001g0275 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.959+4721C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878427 | |||||||
| chr11:878488 | A | C | 1 | a0001c0001t0001g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.959+4660T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878488 | |||||||
| chr11:878562 | TA | T | 7 | a0001c0001t0001g0115 a0001c0001t0001g0135 a0002c0002t0001g0229 others(4): Show |
7 | HG01070.hp2 HG02965.hp1 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.959+4585delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878562 | |||||||
| chr11:878598 | TCA | T | 2 | a0002c0002t0001g0032 a0002c0002t0001g0274 |
3 | HG00733.hp1 HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.959+4548_959+4549d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878598 | |||||||
| chr11:878634 | G | A | 1 | a0002c0002t0024g0268 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.959+4514C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878634 | |||||||
| chr11:878848 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+4300C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878848 | |||||||
| chr11:878858 | T | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0145 |
3 | HG01934.hp2 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.959+4290A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878858 | |||||||
| chr11:878859 | T | A | 1 | a0001c0001t0019g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.959+4289A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 878859 | |||||||
| chr11:879003 | C | T | 10 | a0002c0002t0001g0007 a0002c0002t0001g0040 a0002c0002t0001g0074 others(7): Show |
12 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.959+4145G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879003 | |||||||
| chr11:879081 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(194): Show |
240 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.959+4067A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879081 | |||||||
| chr11:879125 | T | C | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+4023A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879125 | |||||||
| chr11:879142 | G | A | 1 | a0001c0001t0003g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.959+4006C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879142 | |||||||
| chr11:879375 | T | C | 1 | a0002c0002t0001g0307 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.959+3773A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879375 | |||||||
| chr11:879497 | G | GGGAGAAG others(77): Show |
194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
237 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.959+3650_959+3651i others(86): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879497 | |||||||
| chr11:879497 | G | GGGAGAAG others(77): Show |
1 | a0001c0001t0001g0305 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.959+3650_959+3651i others(86): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879497 | |||||||
| chr11:879497 | G | GGGAGAAG others(77): Show |
2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG00621.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.959+3650_959+3651i others(86): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879497 | |||||||
| chr11:879508 | G | C | 1 | a0002c0002t0001g0307 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.959+3640C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879508 | |||||||
| chr11:879587 | C | T | 10 | a0002c0002t0001g0007 a0002c0002t0001g0040 a0002c0002t0001g0074 others(7): Show |
12 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.959+3561G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879587 | |||||||
| chr11:879691 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+3457C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879691 | |||||||
| chr11:879820 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.959+3328A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879820 | |||||||
| chr11:879921 | G | A | 2 | a0001c0001t0007g0122 a0001c0001t0007g0215 |
2 | HG00140.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.959+3227C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 879921 | |||||||
| chr11:880069 | C | G | 2 | a0001c0001t0001g0094 a0002c0002t0024g0268 |
2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.959+3079G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880069 | |||||||
| chr11:880103 | C | T | 1 | a0002c0002t0001g0288 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.959+3045G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880103 | |||||||
| chr11:880172 | G | A | 2 | a0004c0004t0001g0041 a0004c0004t0001g0309 |
2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.959+2976C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880172 | |||||||
| chr11:880178 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+2970C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880178 | |||||||
| chr11:880272 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0112 |
3 | HG01069.hp1 HG01071.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.959+2876G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880272 | |||||||
| chr11:880318 | C | T | 121 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0192 others(118): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.959+2830G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880318 | |||||||
| chr11:880419 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
99 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.959+2729G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880419 | |||||||
| chr11:880461 | A | T | 1 | a0002c0002t0001g0034 | 2 | HG01255.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.959+2687T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880461 | |||||||
| chr11:880467 | G | A | 121 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0192 others(118): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.959+2681C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880467 | |||||||
| chr11:880705 | C | T | 1 | a0002c0002t0024g0268 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.959+2443G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880705 | |||||||
| chr11:880847 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.959+2301A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 880847 | |||||||
| chr11:881117 | C | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
239 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.959+2031G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881117 | |||||||
| chr11:881182 | G | A | 1 | a0002c0002t0001g0245 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.959+1966C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881182 | |||||||
| chr11:881184 | G | A | 1 | a0002c0002t0001g0260 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.959+1964C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881184 | |||||||
| chr11:881191 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.959+1957G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881191 | |||||||
| chr11:881277 | T | C | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+1871A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881277 | |||||||
| chr11:881286 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.959+1862T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881286 | |||||||
| chr11:881339 | C | T | 1 | a0002c0002t0001g0227 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.959+1809G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881339 | |||||||
| chr11:881369 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.959+1779G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881369 | |||||||
| chr11:881420 | C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+1728G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881420 | |||||||
| chr11:881441 | CACGTCGG others(27): Show |
C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(144): Show |
182 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.959+1673_959+1706d others(36): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881441 | |||||||
| chr11:881451 | G | A | 1 | a0002c0002t0015g0085 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.959+1697C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881451 | |||||||
| chr11:881457 | CTGGGTGG others(101): Show |
C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0028 |
3 | HG03490.hp2 HG03492.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.959+1583_959+1690d others(2): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881457 | |||||||
| chr11:881457 | CTGGGTGG others(138): Show |
C | 27 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0002g0019 others(24): Show |
30 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.959+1546_959+1690d others(2): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881457 | |||||||
| chr11:881475 | G | GACC | 20 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0094 others(17): Show |
22 | HG00597.hp1 HG01070.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | |||||||
| chr11:881475 | G | GACCACGT others(33): Show |
2 | a0001c0001t0001g0171 a0001c0001t0001g0183 |
2 | NA18978.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.959+1672_959+1673i others(42): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | |||||||
| chr11:881475 | G | GACCACGT others(70): Show |
1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+1672_959+1673i others(79): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | |||||||
| chr11:881475 | G | GACCACGT others(70): Show |
10 | a0001c0001t0001g0008 a0001c0001t0001g0107 a0001c0001t0001g0108 others(7): Show |
12 | HG01361.hp2 HG02071.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(79): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | |||||||
| chr11:881475 | G | GACCACGT others(107): Show |
3 | a0002c0002t0001g0033 a0002c0002t0001g0208 a0002c0002t0001g0310 |
3 | HG00609.hp1 HG01928.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.959+1672_959+1673i others(116): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | |||||||
| chr11:881475 | G | GACCACGT others(144): Show |
8 | a0002c0002t0001g0001 a0002c0002t0001g0196 a0002c0002t0001g0223 others(5): Show |
8 | HG00673.hp1 NA18945.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(153): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | |||||||
| chr11:881475 | G | GACCACGT others(181): Show |
60 | a0001c0001t0001g0192 a0001c0001t0009g0255 a0002c0002t0001g0001 others(57): Show |
73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(190): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | |||||||
| chr11:881475 | G | GACCACGT others(218): Show |
38 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0267 others(35): Show |
42 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(227): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | |||||||
| chr11:881475 | G | GACCACGT others(255): Show |
5 | a0002c0002t0001g0001 a0002c0002t0001g0036 a0002c0002t0001g0222 others(2): Show |
5 | HG01167.hp2 HG02273.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.959+1672_959+1673i others(264): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881475 | |||||||
| chr11:881476 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.959+1672T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881476 | |||||||
| chr11:881490 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+1658C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881490 | |||||||
| chr11:881497 | G | GGTGAGGG others(141): Show |
1 | a0002c0002t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.959+1650_959+1651i others(150): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881497 | |||||||
| chr11:881520 | G | A | 3 | a0002c0002t0001g0015 a0002c0002t0001g0079 a0002c0002t0012g0050 |
4 | HG02258.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+1628C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881520 | |||||||
| chr11:881528 | CTGGGTGG others(30): Show |
C | 1 | a0002c0002t0001g0225 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.959+1583_959+1619d others(39): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881528 | |||||||
| chr11:881545 | GGACCACG others(104): Show |
G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0063 a0001c0001t0001g0115 others(3): Show |
8 | HG02155.hp1 NA18957.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.959+1492_959+1602d others(2): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881545 | |||||||
| chr11:881565 | T | C | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(269): Show |
330 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.959+1583A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881565 | |||||||
| chr11:881582 | GGACCACG others(67): Show |
G | 10 | a0001c0001t0001g0094 a0001c0001t0001g0128 a0001c0001t0001g0147 others(7): Show |
10 | HG00597.hp1 HG01192.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.959+1492_959+1565d others(76): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881582 | |||||||
| chr11:881602 | T | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
335 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.959+1546A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881602 | |||||||
| chr11:881639 | T | C | 146 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0100 others(143): Show |
170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.959+1509A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881639 | |||||||
| chr11:881647 | T | TGAGGGAA others(182): Show |
1 | a0002c0002t0001g0227 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.959+1500_959+1501i others(191): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881647 | |||||||
| chr11:881651 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
228 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.959+1497T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881651 | |||||||
| chr11:881656 | T | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(181): Show |
224 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(221): Show |
intron_variant | MODIFIER | c.959+1492A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881656 | |||||||
| chr11:881998 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.959+1150A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 881998 | |||||||
| chr11:882003 | C | CA | 12 | a0001c0001t0001g0018 a0001c0001t0001g0063 a0001c0001t0001g0098 others(9): Show |
13 | HG02027.hp2 HG02055.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.959+1144dupT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882003 | |||||||
| chr11:882003 | CA | C | 20 | a0001c0001t0001g0070 a0001c0001t0001g0103 a0001c0001t0001g0104 others(17): Show |
20 | HG01070.hp1 HG01255.hp1 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.959+1144delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882003 | |||||||
| chr11:882003 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0007g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.959+1135_959+1144d others(12): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882003 | |||||||
| chr11:882036 | A | T | 1 | a0002c0002t0001g0287 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.959+1112T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882036 | |||||||
| chr11:882049 | C | T | 1 | a0001c0001t0030g0321 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.959+1099G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882049 | |||||||
| chr11:882065 | C | G | 1 | a0001c0001t0001g0150 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.959+1083G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882065 | |||||||
| chr11:882142 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0124 a0001c0001t0001g0137 others(1): Show |
7 | HG02280.hp1 HG02630.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.959+1006G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882142 | |||||||
| chr11:882181 | A | C | 1 | a0002c0002t0001g0283 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.959+967T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882181 | |||||||
| chr11:882187 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.959+961G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882187 | |||||||
| chr11:882406 | C | T | 25 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0002g0019 others(22): Show |
27 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.959+742G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882406 | |||||||
| chr11:882455 | G | C | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+693C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882455 | |||||||
| chr11:882558 | A | C | 3 | a0002c0002t0001g0222 a0002c0002t0001g0242 a0002c0002t0001g0243 |
3 | HG01167.hp2 HG01192.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.959+590T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882558 | |||||||
| chr11:882656 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.959+492C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882656 | |||||||
| chr11:882731 | A | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.959+417T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882731 | |||||||
| chr11:882755 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.959+393T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882755 | |||||||
| chr11:882860 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.959+288A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882860 | |||||||
| chr11:882863 | T | C | 1 | a0002c0002t0001g0031 | 2 | NA18960.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.959+285A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882863 | |||||||
| chr11:882900 | CCAGCCTC others(15): Show |
C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0107 a0001c0001t0001g0108 others(3): Show |
8 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.959+226_959+247del others(22): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 882900 | |||||||
| chr11:883058 | G | A | 1 | a0001c0001t0019g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.959+90C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 883058 | |||||||
| chr11:883079 | T | A | 2 | a0001c0001t0030g0321 a0001c0001t0031g0320 |
2 | HG02129.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.959+69A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 883079 | |||||||
| chr11:883124 | C | T | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.959+24G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 883124 | |||||||
| chr11:883131 | G | A | 3 | a0002c0002t0001g0015 a0002c0002t0001g0079 a0002c0002t0012g0050 |
4 | HG02258.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+17C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 10/12 | chr11 | 883131 | |||||||
| chr11:883364 | T | C | 1 | a0002c0002t0015g0085 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.804-61A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883364 | |||||||
| chr11:883384 | G | A | 2 | a0002c0002t0001g0032 a0002c0002t0001g0274 |
3 | HG00733.hp1 HG01074.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.804-81C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883384 | |||||||
| chr11:883391 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.804-88G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883391 | |||||||
| chr11:883394 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.804-91G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883394 | |||||||
| chr11:883479 | G | C | 121 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0192 others(118): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.804-176C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883479 | |||||||
| chr11:883592 | G | A | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
239 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.804-289C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883592 | |||||||
| chr11:883606 | C | A | 1 | a0001c0001t0007g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.804-303G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883606 | |||||||
| chr11:883614 | C | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0107 a0001c0001t0001g0109 others(2): Show |
7 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.804-311G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883614 | |||||||
| chr11:883788 | G | C | 1 | a0002c0002t0001g0073 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.803+280C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883788 | |||||||
| chr11:883843 | C | T | 1 | a0002c0002t0001g0087 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.803+225G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883843 | |||||||
| chr11:883930 | T | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.803+138A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 883930 | |||||||
| chr11:884002 | A | G | 3 | a0002c0002t0001g0285 a0002c0002t0001g0286 a0002c0002t0001g0299 |
3 | HG00735.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.803+66T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 9/12 | chr11 | 884002 | |||||||
| chr11:884193 | C | T | 26 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0002g0019 others(23): Show |
28 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.702-24G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884193 | |||||||
| chr11:884346 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.702-177C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884346 | |||||||
| chr11:884369 | A | T | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.702-200T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884369 | |||||||
| chr11:884543 | T | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
99 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.702-374A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884543 | |||||||
| chr11:884743 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.702-574G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884743 | |||||||
| chr11:884780 | C | T | 121 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0192 others(118): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.702-611G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884780 | |||||||
| chr11:884808 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.702-639C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884808 | |||||||
| chr11:884900 | C | A | 1 | a0002c0002t0001g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.702-731G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 884900 | |||||||
| chr11:885064 | G | A | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.702-895C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885064 | |||||||
| chr11:885078 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.702-909A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885078 | |||||||
| chr11:885189 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.702-1020G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885189 | |||||||
| chr11:885253 | G | A | 121 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0192 others(118): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.702-1084C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885253 | |||||||
| chr11:885305 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.702-1136G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885305 | |||||||
| chr11:885319 | T | G | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.702-1150A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885319 | |||||||
| chr11:885330 | C | A | 121 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0192 others(118): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.702-1161G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885330 | |||||||
| chr11:885435 | C | T | 1 | a0001c0001t0021g0106 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.702-1266G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885435 | |||||||
| chr11:885473 | CA | C | 3 | a0002c0002t0001g0015 a0002c0002t0001g0079 a0002c0002t0012g0050 |
4 | HG02258.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.702-1305delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885473 | |||||||
| chr11:885480 | G | A | 60 | a0001c0001t0001g0192 a0001c0001t0009g0255 a0002c0002t0001g0001 others(57): Show |
75 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.702-1311C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885480 | |||||||
| chr11:885542 | C | T | 2 | a0002c0002t0001g0248 a0002c0002t0001g0292 |
2 | HG01361.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.702-1373G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885542 | |||||||
| chr11:885553 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.702-1384A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885553 | |||||||
| chr11:885564 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
239 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.702-1395A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885564 | |||||||
| chr11:885637 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.702-1468G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885637 | |||||||
| chr11:885685 | T | C | 121 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0192 others(118): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.702-1516A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885685 | |||||||
| chr11:885695 | C | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
237 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.702-1526G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885695 | |||||||
| chr11:885716 | C | T | 2 | a0001c0001t0001g0267 a0001c0001t0001g0278 |
2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.702-1547G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885716 | |||||||
| chr11:885949 | G | A | 1 | a0002c0002t0001g0274 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.702-1780C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 885949 | |||||||
| chr11:886145 | C | T | 1 | a0002c0002t0001g0219 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.702-1976G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886145 | |||||||
| chr11:886150 | C | CA | 5 | a0001c0001t0001g0162 a0001c0001t0002g0062 a0001c0001t0002g0190 others(2): Show |
5 | HG01074.hp1 HG02257.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.702-1982dupT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886150 | |||||||
| chr11:886157 | AG | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0026 others(141): Show |
169 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.702-1989delC | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886157 | |||||||
| chr11:886158 | G | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
211 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.702-1989C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886158 | |||||||
| chr11:886170 | G | A | 6 | a0001c0001t0001g0059 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
6 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.702-2001C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886170 | |||||||
| chr11:886172 | A | G | 6 | a0001c0001t0001g0059 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
6 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.702-2003T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886172 | |||||||
| chr11:886176 | AT | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
177 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.702-2008delA | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886176 | |||||||
| chr11:886177 | T | A | 6 | a0001c0001t0001g0059 a0001c0001t0001g0104 a0001c0001t0001g0105 others(3): Show |
6 | HG00735.hp1 HG00741.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.702-2008A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886177 | |||||||
| chr11:886191 | G | T | 9 | a0001c0001t0001g0024 a0001c0001t0001g0080 a0001c0001t0001g0146 others(6): Show |
10 | HG00438.hp2 HG00597.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.702-2022C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886191 | |||||||
| chr11:886453 | T | C | 6 | a0002c0002t0001g0033 a0002c0002t0001g0084 a0002c0002t0001g0275 others(3): Show |
7 | HG01070.hp1 HG01346.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.702-2284A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886453 | |||||||
| chr11:886690 | C | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0124 a0001c0001t0001g0137 others(1): Show |
7 | HG02280.hp1 HG02630.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.702-2521G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886690 | |||||||
| chr11:886695 | C | T | 3 | a0001c0001t0002g0046 a0001c0001t0002g0313 a0001c0001t0002g0314 |
3 | HG02486.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.702-2526G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886695 | |||||||
| chr11:886709 | C | T | 1 | a0002c0002t0001g0319 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.702-2540G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886709 | |||||||
| chr11:886730 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.702-2561C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886730 | |||||||
| chr11:886752 | T | C | 1 | a0002c0002t0001g0086 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.702-2583A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886752 | |||||||
| chr11:886869 | A | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.702-2700T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 886869 | |||||||
| chr11:887102 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.702-2933G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887102 | |||||||
| chr11:887220 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702-3051C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887220 | |||||||
| chr11:887225 | A | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.702-3056T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887225 | |||||||
| chr11:887322 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702-3153C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887322 | |||||||
| chr11:887402 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.702-3233T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887402 | |||||||
| chr11:887420 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702-3251C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887420 | |||||||
| chr11:887431 | G | T | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.702-3262C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887431 | |||||||
| chr11:887458 | G | T | 25 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0002g0019 others(22): Show |
27 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.702-3289C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887458 | |||||||
| chr11:887560 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | HG01261.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.702-3391G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887560 | |||||||
| chr11:887561 | C | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702-3392G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887561 | |||||||
| chr11:887741 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.702-3572A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887741 | |||||||
| chr11:887977 | C | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.702-3808G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 887977 | |||||||
| chr11:888068 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0123 |
3 | NA18944.hp1 NA18989.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.702-3899C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888068 | |||||||
| chr11:888086 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0120 |
2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.702-3917A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888086 | |||||||
| chr11:888115 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.702-3946G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888115 | |||||||
| chr11:888150 | T | C | 124 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0094 others(121): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.702-3981A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888150 | |||||||
| chr11:888187 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.702-4018C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888187 | |||||||
| chr11:888188 | A | G | 1 | a0001c0001t0001g0317 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.702-4019T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888188 | |||||||
| chr11:888339 | T | C | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.702-4170A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888339 | |||||||
| chr11:888533 | G | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
237 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.702-4364C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888533 | |||||||
| chr11:888632 | G | A | 123 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0094 others(120): Show |
145 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.702-4463C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888632 | |||||||
| chr11:888716 | C | G | 1 | a0001c0001t0028g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.702-4547G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888716 | |||||||
| chr11:888740 | T | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.702-4571A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888740 | |||||||
| chr11:888759 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.702-4590G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888759 | |||||||
| chr11:888760 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.702-4591C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888760 | |||||||
| chr11:888833 | T | TGCCAGTG others(91): Show |
1 | a0002c0002t0001g0251 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.701+4593_701+4594i others(100): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888833 | |||||||
| chr11:888858 | G | A | 1 | a0002c0002t0001g0273 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.701+4569C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888858 | |||||||
| chr11:888957 | G | A | 121 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0192 others(118): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.701+4470C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 888957 | |||||||
| chr11:889112 | C | T | 1 | a0001c0001t0019g0051 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.701+4315G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 889112 | |||||||
| chr11:889137 | C | T | 2 | a0002c0002t0001g0223 a0002c0002t0001g0224 |
2 | NA18966.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.701+4290G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 889137 | |||||||
| chr11:889138 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.701+4289C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 889138 | |||||||
| chr11:889690 | C | A | 1 | a0002c0002t0008g0194 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.701+3737G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 889690 | |||||||
| chr11:889858 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0181 |
3 | HG00621.hp2 HG02074.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.701+3569C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 889858 | |||||||
| chr11:890048 | C | G | 1 | a0002c0002t0001g0300 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.701+3379G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890048 | |||||||
| chr11:890091 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.701+3336C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890091 | |||||||
| chr11:890131 | G | A | 5 | a0001c0001t0001g0029 a0002c0002t0001g0269 a0002c0002t0001g0270 others(2): Show |
6 | HG00642.hp1 HG02258.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.701+3296C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890131 | |||||||
| chr11:890197 | C | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0010 others(31): Show |
49 | HG00558.hp1 HG00621.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.701+3230G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890197 | |||||||
| chr11:890263 | C | G | 1 | a0003c0003t0002g0099 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.701+3164G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890263 | |||||||
| chr11:890275 | CCT | C | 5 | a0002c0002t0001g0037 a0002c0002t0001g0289 a0002c0002t0001g0297 others(2): Show |
6 | HG01346.hp2 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.701+3150_701+3151d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890275 | |||||||
| chr11:890355 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.701+3072C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890355 | |||||||
| chr11:890405 | T | C | 128 | a0001c0001t0001g0024 a0001c0001t0001g0070 a0001c0001t0001g0072 others(125): Show |
151 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.701+3022A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890405 | |||||||
| chr11:890673 | AC | A | 10 | a0002c0002t0001g0007 a0002c0002t0001g0040 a0002c0002t0001g0074 others(7): Show |
12 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.701+2753delG | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890673 | |||||||
| chr11:890779 | T | G | 2 | a0002c0002t0001g0075 a0002c0002t0001g0076 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.701+2648A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890779 | |||||||
| chr11:890864 | A | G | 1 | a0002c0002t0001g0248 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.701+2563T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890864 | |||||||
| chr11:890866 | G | A | 1 | a0002c0002t0001g0279 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.701+2561C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890866 | |||||||
| chr11:890906 | A | G | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+2521T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890906 | |||||||
| chr11:890985 | T | TGCTCTTG others(37): Show |
1 | a0001c0001t0001g0169 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.701+2398_701+2441d others(46): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 890985 | |||||||
| chr11:891019 | C | T | 1 | a0002c0002t0001g0281 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.701+2408G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891019 | |||||||
| chr11:891094 | G | A | 2 | a0001c0001t0001g0162 a0002c0002t0010g0236 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.701+2333C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891094 | |||||||
| chr11:891106 | A | AAC | 78 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0001g0290 others(75): Show |
91 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.701+2319_701+2320d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891106 | |||||||
| chr11:891157 | G | A | 3 | a0002c0002t0001g0277 a0002c0006t0006g0125 a0002c0007t0006g0126 |
3 | HG03139.hp2 NA19043.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.701+2270C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891157 | |||||||
| chr11:891189 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.701+2238G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891189 | |||||||
| chr11:891196 | G | A | 1 | a0002c0002t0001g0260 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.701+2231C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891196 | |||||||
| chr11:891326 | G | A | 4 | a0002c0002t0001g0230 a0002c0002t0001g0231 a0002c0002t0001g0232 others(1): Show |
4 | NA18960.hp2 NA19058.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+2101C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891326 | |||||||
| chr11:891328 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.701+2099G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891328 | |||||||
| chr11:891331 | C | T | 1 | a0002c0002t0001g0034 | 2 | HG01255.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.701+2096G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891331 | |||||||
| chr11:891338 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
197 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.701+2089C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891338 | |||||||
| chr11:891384 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+2043C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891384 | |||||||
| chr11:891417 | G | A | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+2010C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891417 | |||||||
| chr11:891438 | T | C | 3 | a0001c0001t0001g0133 a0001c0001t0001g0142 a0001c0001t0001g0144 |
3 | HG01358.hp1 HG02698.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.701+1989A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891438 | |||||||
| chr11:891512 | G | A | 3 | a0002c0002t0001g0037 a0002c0002t0001g0303 a0002c0002t0001g0304 |
4 | HG01346.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+1915C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891512 | |||||||
| chr11:891571 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(72): Show |
98 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.701+1856G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891571 | |||||||
| chr11:891689 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.701+1738C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891689 | |||||||
| chr11:891732 | C | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0107 a0001c0001t0001g0109 others(2): Show |
7 | HG02280.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.701+1695G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891732 | |||||||
| chr11:891734 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.701+1693A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891734 | |||||||
| chr11:891853 | C | T | 25 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0002g0019 others(22): Show |
27 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.701+1574G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891853 | |||||||
| chr11:891854 | G | A | 2 | a0002c0002t0001g0306 a0002c0002t0001g0308 |
2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.701+1573C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891854 | |||||||
| chr11:891938 | CA | C | 33 | a0001c0001t0001g0021 a0001c0001t0001g0059 a0001c0001t0001g0094 others(30): Show |
34 | HG00140.hp2 HG00673.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.701+1488delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891938 | |||||||
| chr11:891938 | CAA | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(220): Show |
274 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.701+1487_701+1488d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891938 | |||||||
| chr11:891938 | CAAA | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0016 others(28): Show |
42 | HG00558.hp1 HG00621.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.701+1486_701+1488d others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891938 | |||||||
| chr11:891938 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0239 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.701+1477_701+1488d others(14): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891938 | |||||||
| chr11:891953 | A | G | 1 | a0002c0002t0001g0234 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.701+1474T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891953 | |||||||
| chr11:891956 | A | C | 1 | a0001c0001t0001g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.701+1471T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891956 | |||||||
| chr11:891960 | A | C | 111 | a0001c0001t0001g0094 a0001c0001t0001g0192 a0001c0001t0001g0267 others(108): Show |
133 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.701+1467T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891960 | |||||||
| chr11:891970 | A | C | 1 | a0001c0001t0001g0240 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.701+1457T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891970 | |||||||
| chr11:891972 | T | C | 16 | a0001c0001t0001g0100 a0001c0001t0002g0019 a0001c0001t0002g0025 others(13): Show |
18 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.701+1455A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891972 | |||||||
| chr11:891977 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.701+1450C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891977 | |||||||
| chr11:891983 | A | G | 112 | a0001c0001t0001g0094 a0001c0001t0001g0192 a0001c0001t0001g0267 others(109): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.701+1444T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 891983 | |||||||
| chr11:892062 | A | G | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+1365T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892062 | |||||||
| chr11:892089 | T | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(178): Show |
222 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(219): Show |
intron_variant | MODIFIER | c.701+1338A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892089 | |||||||
| chr11:892095 | A | T | 1 | a0001c0001t0001g0174 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.701+1332T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892095 | |||||||
| chr11:892110 | A | G | 61 | a0001c0001t0001g0192 a0001c0001t0001g0290 a0001c0001t0009g0255 others(58): Show |
76 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.701+1317T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892110 | |||||||
| chr11:892161 | C | A | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.701+1266G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892161 | |||||||
| chr11:892212 | G | A | 1 | a0002c0002t0001g0297 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.701+1215C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892212 | |||||||
| chr11:892327 | C | T | 1 | a0002c0002t0001g0310 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.701+1100G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892327 | |||||||
| chr11:892461 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.701+966A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892461 | |||||||
| chr11:892465 | C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+962G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892465 | |||||||
| chr11:892497 | C | G | 1 | a0002c0002t0001g0234 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.701+930G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892497 | |||||||
| chr11:892611 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.701+816C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892611 | |||||||
| chr11:892648 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.701+779G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892648 | |||||||
| chr11:892760 | A | G | 109 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(106): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.701+667T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892760 | |||||||
| chr11:892766 | G | C | 2 | a0001c0001t0001g0094 a0002c0002t0024g0268 |
2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.701+661C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 892766 | |||||||
| chr11:893152 | G | A | 72 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(69): Show |
86 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.701+275C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 893152 | |||||||
| chr11:893299 | T | C | 109 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(106): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.701+128A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 893299 | |||||||
| chr11:893417 | C | T | 1 | a0002c0002t0001g0300 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.701+10G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 8/12 | chr11 | 893417 | |||||||
| chr11:893588 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.609-69G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893588 | |||||||
| chr11:893708 | GC | G | 24 | a0001c0001t0001g0100 a0001c0001t0002g0019 a0001c0001t0002g0025 others(21): Show |
26 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.609-190delG | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893708 | |||||||
| chr11:893715 | T | C | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.609-196A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893715 | |||||||
| chr11:893872 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.609-353G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893872 | |||||||
| chr11:893925 | C | T | 2 | a0002c0002t0001g0038 a0002c0002t0001g0254 |
3 | HG00639.hp1 HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.609-406G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893925 | |||||||
| chr11:893928 | C | CTTGGCCA others(31): Show |
1 | a0001c0001t0001g0318 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.609-447_609-410dup others(38): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893928 | |||||||
| chr11:893984 | T | C | 109 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(106): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.609-465A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 893984 | |||||||
| chr11:894058 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.609-539C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894058 | |||||||
| chr11:894121 | CA | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
98 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.609-603delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | |||||||
| chr11:894121 | CAA | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(78): Show |
100 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.609-604_609-603del others(2): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | |||||||
| chr11:894121 | CAAA | C | 92 | a0001c0001t0001g0022 a0001c0001t0001g0129 a0001c0001t0001g0130 others(89): Show |
114 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.609-605_609-603del others(3): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | |||||||
| chr11:894121 | CAAAAAA | C | 4 | a0001c0001t0003g0017 a0001c0001t0003g0078 a0002c0002t0001g0015 others(1): Show |
6 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.609-608_609-603del others(6): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | |||||||
| chr11:894121 | CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0054 others(4): Show |
7 | HG02074.hp2 HG02129.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.609-612_609-603del others(10): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | |||||||
| chr11:894121 | CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0047 |
4 | HG02004.hp2 HG04228.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-618_609-603del others(16): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894121 | |||||||
| chr11:894132 | A | G | 2 | a0001c0001t0002g0046 a0001c0001t0002g0102 |
2 | HG02486.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.609-613T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894132 | |||||||
| chr11:894132 | A | T | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.609-613T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894132 | |||||||
| chr11:894133 | A | G | 20 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0002g0019 others(17): Show |
22 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.609-614T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894133 | |||||||
| chr11:894134 | A | G | 3 | a0003c0003t0001g0152 a0003c0003t0001g0153 a0003c0003t0002g0154 |
3 | HG00140.hp1 HG01106.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.609-615T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894134 | |||||||
| chr11:894205 | T | C | 109 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(106): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.609-686A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894205 | |||||||
| chr11:894832 | A | C | 1 | a0002c0002t0001g0068 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.609-1313T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894832 | |||||||
| chr11:894874 | A | G | 180 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(177): Show |
221 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.609-1355T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894874 | |||||||
| chr11:894885 | C | A | 1 | a0002c0002t0001g0040 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.609-1366G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 894885 | |||||||
| chr11:895014 | C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.609-1495G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895014 | |||||||
| chr11:895070 | C | T | 1 | a0002c0002t0001g0301 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.609-1551G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895070 | |||||||
| chr11:895144 | G | C | 1 | a0001c0001t0001g0059 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.609-1625C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895144 | |||||||
| chr11:895176 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.609-1657T>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895176 | |||||||
| chr11:895453 | G | T | 1 | a0002c0002t0001g0087 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.609-1934C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895453 | |||||||
| chr11:895490 | C | T | 2 | a0002c0002t0001g0306 a0002c0002t0001g0308 |
2 | HG00738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.609-1971G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895490 | |||||||
| chr11:895596 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(45): Show |
60 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.609-2077G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895596 | |||||||
| chr11:895744 | C | G | 110 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(107): Show |
132 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.609-2225G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895744 | |||||||
| chr11:895792 | G | A | 1 | a0002c0002t0001g0079 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.609-2273C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895792 | |||||||
| chr11:895881 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.609-2362C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895881 | |||||||
| chr11:895982 | T | C | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.609-2463A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 895982 | |||||||
| chr11:896025 | C | T | 2 | a0001c0001t0001g0094 a0002c0002t0024g0268 |
2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.609-2506G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896025 | |||||||
| chr11:896081 | C | T | 109 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(106): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.609-2562G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896081 | |||||||
| chr11:896082 | GCAGCCTC others(619): Show |
G | 7 | a0001c0001t0001g0008 a0001c0001t0001g0107 a0001c0001t0001g0108 others(4): Show |
9 | HG02109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.608+2632_609-2564d others(2): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896082 | |||||||
| chr11:896143 | G | A | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.609-2624C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896143 | |||||||
| chr11:896275 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.609-2756G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896275 | |||||||
| chr11:896300 | C | G | 17 | a0002c0002t0001g0006 a0002c0002t0001g0038 a0002c0002t0001g0193 others(14): Show |
21 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.609-2781G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896300 | |||||||
| chr11:896459 | AAGGCTGT others(31): Show |
A | 2 | a0002c0002t0001g0040 a0002c0002t0001g0198 |
2 | HG01943.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.608+2843_608+2880d others(40): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896459 | |||||||
| chr11:896495 | ATGAGGCT others(31): Show |
A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0002c0002t0001g0246 |
3 | HG03710.hp2 HG06807.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.608+2807_608+2844d others(40): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896495 | |||||||
| chr11:896496 | T | C | 108 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(105): Show |
130 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.608+2844A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896496 | |||||||
| chr11:896532 | C | T | 1 | a0002c0002t0001g0298 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.608+2808G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896532 | |||||||
| chr11:896534 | T | C | 1 | a0002c0002t0001g0246 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.608+2806A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896534 | |||||||
| chr11:896548 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0112 |
3 | HG01069.hp1 HG01071.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.608+2792G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896548 | |||||||
| chr11:896553 | C | A | 1 | a0001c0001t0001g0238 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.608+2787G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896553 | |||||||
| chr11:896587 | ACCCCCAG others(34): Show |
A | 1 | a0001c0001t0002g0027 | 2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.608+2712_608+2752d others(43): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896587 | |||||||
| chr11:896718 | C | G | 109 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(106): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.608+2622G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896718 | |||||||
| chr11:896726 | G | A | 34 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0028 others(31): Show |
39 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.608+2614C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896726 | |||||||
| chr11:896763 | C | T | 71 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(68): Show |
85 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.608+2577G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896763 | |||||||
| chr11:896806 | T | C | 1 | a0001c0001t0002g0314 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.608+2534A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896806 | |||||||
| chr11:896821 | G | A | 1 | a0002c0002t0001g0253 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.608+2519C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896821 | |||||||
| chr11:896845 | T | G | 109 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(106): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.608+2495A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896845 | |||||||
| chr11:896867 | ACTCCACC others(31): Show |
A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0238 a0002c0002t0024g0268 |
3 | HG01192.hp1 HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.608+2435_608+2472d others(40): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896867 | |||||||
| chr11:896875 | C | A | 1 | a0002c0002t0001g0282 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.608+2465G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896875 | |||||||
| chr11:896904 | G | C | 1 | a0001c0001t0016g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.608+2436C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896904 | |||||||
| chr11:896911 | C | CCCCAGAC others(34): Show |
1 | a0001c0001t0001g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.608+2428_608+2429i others(43): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896911 | |||||||
| chr11:896918 | C | CACA | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
247 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.608+2421_608+2422i others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896918 | |||||||
| chr11:896949 | C | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
247 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.608+2391G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896949 | |||||||
| chr11:896952 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0077 a0002c0002t0001g0082 |
4 | HG02572.hp2 HG02647.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.608+2388G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896952 | |||||||
| chr11:896956 | CACA | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
247 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.608+2381_608+2383d others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896956 | |||||||
| chr11:896979 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.608+2361G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896979 | |||||||
| chr11:896980 | C | G | 1 | a0001c0001t0001g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.608+2360G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896980 | |||||||
| chr11:896990 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2350A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896990 | |||||||
| chr11:896993 | C | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
247 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.608+2347G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896993 | |||||||
| chr11:896995 | G | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
247 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.608+2345C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896995 | |||||||
| chr11:896997 | C | CA | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
247 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.608+2342dupT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896997 | |||||||
| chr11:896999 | C | T | 1 | a0001c0001t0028g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.608+2341G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 896999 | |||||||
| chr11:897017 | C | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2323G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897017 | |||||||
| chr11:897018 | C | G | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2322G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897018 | |||||||
| chr11:897031 | G | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2309C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897031 | |||||||
| chr11:897033 | C | G | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2307G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897033 | |||||||
| chr11:897035 | CA | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.608+2304delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897035 | |||||||
| chr11:897036 | AACGAGCC others(69): Show |
A | 1 | a0002c0002t0001g0298 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.608+2228_608+2303d others(78): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897036 | |||||||
| chr11:897038 | C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.608+2302G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897038 | |||||||
| chr11:897094 | T | C | 2 | a0001c0001t0001g0144 a0003c0003t0002g0039 |
2 | HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.608+2246A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897094 | |||||||
| chr11:897095 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.608+2245C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897095 | |||||||
| chr11:897114 | C | T | 1 | a0001c0001t0021g0106 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.608+2226G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897114 | |||||||
| chr11:897181 | C | T | 2 | a0002c0006t0006g0125 a0002c0007t0006g0126 |
2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.608+2159G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897181 | |||||||
| chr11:897193 | C | T | 109 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(106): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.608+2147G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897193 | |||||||
| chr11:897306 | G | A | 1 | a0001c0001t0023g0151 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.608+2034C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897306 | |||||||
| chr11:897589 | A | C | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG06807.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.608+1751T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897589 | |||||||
| chr11:897655 | C | A | 1 | a0001c0001t0002g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.608+1685G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897655 | |||||||
| chr11:897691 | T | A | 17 | a0002c0002t0001g0006 a0002c0002t0001g0038 a0002c0002t0001g0193 others(14): Show |
21 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.608+1649A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897691 | |||||||
| chr11:897692 | C | T | 17 | a0002c0002t0001g0006 a0002c0002t0001g0038 a0002c0002t0001g0193 others(14): Show |
21 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.608+1648G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897692 | |||||||
| chr11:897809 | C | T | 1 | a0002c0002t0001g0280 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.608+1531G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897809 | |||||||
| chr11:897825 | A | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.608+1515T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897825 | |||||||
| chr11:897981 | C | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(44): Show |
59 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.608+1359G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897981 | |||||||
| chr11:897995 | G | C | 2 | a0001c0001t0001g0094 a0002c0002t0024g0268 |
2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.608+1345C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 897995 | |||||||
| chr11:898074 | A | C | 1 | a0002c0002t0001g0300 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.608+1266T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898074 | |||||||
| chr11:898099 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.608+1241C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898099 | |||||||
| chr11:898135 | G | A | 9 | a0002c0002t0001g0212 a0002c0002t0001g0219 a0002c0002t0001g0220 others(6): Show |
9 | NA18960.hp2 NA18965.hp1 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.608+1205C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898135 | |||||||
| chr11:898155 | T | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
251 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.608+1185A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898155 | |||||||
| chr11:898162 | A | G | 1 | a0002c0002t0024g0268 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.608+1178T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898162 | |||||||
| chr11:898344 | T | C | 25 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0002g0019 others(22): Show |
27 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.608+996A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898344 | |||||||
| chr11:898352 | G | T | 1 | a0002c0002t0001g0279 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.608+988C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898352 | |||||||
| chr11:898459 | A | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.608+881T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898459 | |||||||
| chr11:898463 | T | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.608+877A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898463 | |||||||
| chr11:898483 | T | C | 1 | a0001c0001t0017g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.608+857A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898483 | |||||||
| chr11:898518 | G | A | 25 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0002g0019 others(22): Show |
27 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.608+822C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898518 | |||||||
| chr11:898643 | C | T | 21 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0002c0002t0001g0007 others(18): Show |
23 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.608+697G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898643 | |||||||
| chr11:898726 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.608+614G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898726 | |||||||
| chr11:898743 | T | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0080 a0001c0001t0001g0146 others(6): Show |
10 | HG00438.hp2 HG00597.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.608+597A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898743 | |||||||
| chr11:898761 | G | T | 2 | a0001c0001t0001g0267 a0001c0001t0001g0278 |
2 | HG02818.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.608+579C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898761 | |||||||
| chr11:898892 | C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.608+448G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898892 | |||||||
| chr11:898979 | T | G | 1 | a0004c0004t0001g0309 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.608+361A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 898979 | |||||||
| chr11:899218 | C | A | 1 | a0002c0002t0001g0272 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.608+122G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 7/12 | chr11 | 899218 | |||||||
| chr11:899567 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.547-166C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 6/12 | chr11 | 899567 | |||||||
| chr11:899580 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.547-179G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 6/12 | chr11 | 899580 | |||||||
| chr11:899627 | G | C | 318 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
383 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.547-226C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 6/12 | chr11 | 899627 | |||||||
| chr11:899814 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.546+190A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 6/12 | chr11 | 899814 | |||||||
| chr11:899973 | C | A | 1 | a0001c0001t0001g0305 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.546+31G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 6/12 | chr11 | 899973 | |||||||
| chr11:900152 | A | G | 1 | a0002c0002t0001g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.440-42T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900152 | |||||||
| chr11:900183 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.440-73T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900183 | |||||||
| chr11:900298 | G | A | 2 | a0004c0004t0001g0041 a0004c0004t0001g0309 |
2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.440-188C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900298 | |||||||
| chr11:900369 | G | A | 25 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0002g0019 others(22): Show |
27 | HG00140.hp1 HG00733.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.440-259C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900369 | |||||||
| chr11:900421 | T | C | 112 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(109): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.440-311A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900421 | |||||||
| chr11:900485 | T | C | 111 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(108): Show |
133 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.440-375A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900485 | |||||||
| chr11:900690 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.439+246G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900690 | |||||||
| chr11:900773 | G | A | 1 | a0004c0004t0001g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.439+163C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900773 | |||||||
| chr11:900809 | G | A | 18 | a0002c0002t0001g0006 a0002c0002t0001g0038 a0002c0002t0001g0193 others(15): Show |
22 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.439+127C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900809 | |||||||
| chr11:900894 | T | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.439+42A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900894 | |||||||
| chr11:900929 | C | G | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
260 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(257): Show |
splice_region_variant&intron_variant | LOW | c.439+7G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 5/12 | chr11 | 900929 | |||||||
| chr11:901023 | C | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0221 |
2 | HG02071.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.395-43G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901023 | |||||||
| chr11:901177 | C | CTTCT | 5 | a0002c0002t0001g0197 a0002c0002t0001g0269 a0002c0002t0001g0270 others(2): Show |
5 | HG00642.hp1 HG02258.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-201_395-198dup others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901177 | |||||||
| chr11:901337 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.395-357G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901337 | |||||||
| chr11:901464 | G | A | 2 | a0004c0004t0001g0041 a0004c0004t0001g0309 |
2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.395-484C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901464 | |||||||
| chr11:901625 | G | A | 3 | a0002c0002t0001g0036 a0002c0002t0001g0300 a0002c0002t0001g0301 |
4 | NA18979.hp1 NA18990.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.394+573C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901625 | |||||||
| chr11:901690 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.394+508C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901690 | |||||||
| chr11:901733 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
7 | HG02004.hp2 HG02683.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.394+465G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901733 | |||||||
| chr11:901912 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.394+286C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901912 | |||||||
| chr11:901935 | CA | C | 317 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(314): Show |
382 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.394+262delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 901935 | |||||||
| chr11:902036 | TACAC | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
248 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.394+158_394+161del others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 902036 | |||||||
| chr11:902045 | A | G | 1 | a0002c0002t0001g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.394+153T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 4/12 | chr11 | 902045 | |||||||
| chr11:902355 | C | T | 5 | a0001c0001t0001g0100 a0001c0001t0002g0019 a0001c0001t0002g0101 others(2): Show |
6 | HG03927.hp1 NA18967.hp1 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-25G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902355 | |||||||
| chr11:902405 | C | T | 23 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0002c0002t0001g0007 others(20): Show |
25 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.262-75G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902405 | |||||||
| chr11:902645 | G | A | 1 | a0002c0002t0001g0196 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.262-315C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902645 | |||||||
| chr11:902668 | AGGGTT | A | 109 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(106): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.261+289_261+293del others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902668 | |||||||
| chr11:902712 | G | A | 3 | a0001c0001t0002g0163 a0004c0004t0001g0041 a0004c0004t0001g0309 |
3 | HG01167.hp1 HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.261+250C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902712 | |||||||
| chr11:902742 | C | G | 1 | a0003c0003t0002g0099 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.261+220G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902742 | |||||||
| chr11:902768 | A | G | 2 | a0001c0001t0001g0018 a0002c0002t0001g0082 |
3 | HG02572.hp2 HG02647.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.261+194T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902768 | |||||||
| chr11:902899 | G | A | 2 | a0004c0004t0001g0041 a0004c0004t0001g0309 |
2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.261+63C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902899 | |||||||
| chr11:902939 | G | A | 109 | a0001c0001t0001g0192 a0001c0001t0001g0267 a0001c0001t0001g0278 others(106): Show |
131 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.261+23C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 3/12 | chr11 | 902939 | |||||||
| chr11:903167 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.112-56G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903167 | |||||||
| chr11:903214 | T | A | 1 | a0002c0002t0001g0302 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.112-103A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903214 | |||||||
| chr11:903216 | T | C | 2 | a0002c0002t0001g0038 a0002c0002t0001g0254 |
3 | HG00639.hp1 HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.112-105A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903216 | |||||||
| chr11:903260 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.112-149C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903260 | |||||||
| chr11:903266 | G | C | 3 | a0002c0002t0001g0037 a0002c0002t0001g0303 a0002c0002t0001g0304 |
4 | HG01346.hp2 HG02717.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.112-155C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903266 | |||||||
| chr11:903326 | T | C | 35 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0028 others(32): Show |
40 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-215A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903326 | |||||||
| chr11:903332 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.112-221C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903332 | |||||||
| chr11:903417 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.112-306C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903417 | |||||||
| chr11:903470 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.112-359G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903470 | |||||||
| chr11:903547 | G | A | 1 | a0002c0002t0001g0306 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.112-436C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903547 | |||||||
| chr11:903576 | T | G | 1 | a0001c0001t0001g0029 | 2 | NA18948.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.112-465A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903576 | |||||||
| chr11:903737 | C | T | 1 | a0001c0001t0016g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.112-626G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903737 | |||||||
| chr11:903750 | C | T | 1 | a0001c0001t0031g0320 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.112-639G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903750 | |||||||
| chr11:903838 | C | T | 1 | a0002c0002t0001g0031 | 2 | NA18960.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.112-727G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903838 | |||||||
| chr11:903847 | G | GC | 8 | a0001c0001t0001g0185 a0001c0001t0001g0206 a0001c0001t0028g0184 others(5): Show |
8 | HG00738.hp1 HG01109.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.112-737dupG | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903847 | |||||||
| chr11:903897 | G | A | 1 | a0002c0002t0001g0235 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.112-786C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903897 | |||||||
| chr11:903977 | C | A | 1 | a0001c0001t0017g0186 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.111+729G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 903977 | |||||||
| chr11:904168 | C | T | 3 | a0002c0002t0001g0222 a0002c0002t0001g0242 a0002c0002t0001g0243 |
3 | HG01167.hp2 HG01192.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.111+538G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904168 | |||||||
| chr11:904258 | G | A | 23 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0002c0002t0001g0007 others(20): Show |
25 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.111+448C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904258 | |||||||
| chr11:904454 | C | A | 25 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0019g0051 others(22): Show |
27 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.111+252G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904454 | |||||||
| chr11:904454 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.111+252G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904454 | |||||||
| chr11:904563 | C | T | 2 | a0002c0002t0001g0030 a0002c0002t0001g0266 |
3 | NA18612.hp1 NA18965.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.111+143G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904563 | |||||||
| chr11:904649 | G | A | 2 | a0004c0004t0001g0041 a0004c0004t0001g0309 |
2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.111+57C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 2/12 | chr11 | 904649 | |||||||
| chr11:904911 | T | C | 138 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0072 others(135): Show |
164 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.-43-52A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 904911 | |||||||
| chr11:905331 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-43-472C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905331 | |||||||
| chr11:905395 | C | T | 1 | a0001c0001t0002g0097 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-43-536G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905395 | |||||||
| chr11:905441 | G | A | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-43-582C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905441 | |||||||
| chr11:905571 | G | A | 1 | a0004c0004t0001g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-43-712C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905571 | |||||||
| chr11:905691 | G | A | 1 | a0002c0002t0001g0310 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-43-832C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905691 | |||||||
| chr11:905719 | C | T | 1 | a0002c0002t0005g0261 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-43-860G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905719 | |||||||
| chr11:905740 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-43-881C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 905740 | |||||||
| chr11:906041 | C | T | 3 | a0001c0001t0002g0046 a0001c0001t0002g0313 a0001c0001t0002g0314 |
3 | HG02486.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-43-1182G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906041 | |||||||
| chr11:906081 | GCCA | G | 3 | a0002c0002t0001g0258 a0002c0002t0001g0259 a0002c0002t0001g0260 |
3 | HG01261.hp1 HG01358.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-43-1225_-43-1223d others(5): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906081 | |||||||
| chr11:906102 | T | C | 1 | a0002c0002t0001g0311 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-43-1243A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906102 | |||||||
| chr11:906173 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-43-1314T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906173 | |||||||
| chr11:906210 | C | T | 3 | a0001c0001t0001g0095 a0002c0002t0001g0201 a0002c0002t0027g0257 |
3 | HG00423.hp2 NA18952.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.-43-1351G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906210 | |||||||
| chr11:906241 | C | CT | 13 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(10): Show |
13 | HG00741.hp1 HG01175.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.-43-1383dupA | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906241 | |||||||
| chr11:906241 | C | CTT | 8 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0042 others(5): Show |
10 | HG02004.hp2 HG02572.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.-43-1384_-43-1383d others(4): Show |
CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906241 | |||||||
| chr11:906310 | C | T | 1 | a0002c0002t0010g0236 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-43-1451G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906310 | |||||||
| chr11:906380 | A | G | 1 | a0004c0004t0001g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-43-1521T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906380 | |||||||
| chr11:906406 | T | G | 1 | a0002c0002t0001g0312 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-43-1547A>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906406 | |||||||
| chr11:906513 | G | A | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-43-1654C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906513 | |||||||
| chr11:906535 | C | T | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-43-1676G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906535 | |||||||
| chr11:906636 | A | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
5 | HG01175.hp2 HG01978.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-1777T>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906636 | |||||||
| chr11:906708 | C | A | 113 | a0001c0001t0001g0018 a0001c0001t0001g0054 a0001c0001t0001g0055 others(110): Show |
132 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.-43-1849G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906708 | |||||||
| chr11:906754 | C | T | 5 | a0002c0002t0001g0223 a0002c0002t0001g0224 a0002c0002t0001g0233 others(2): Show |
5 | NA18951.hp2 NA18966.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.-43-1895G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906754 | |||||||
| chr11:906767 | G | A | 1 | a0002c0002t0001g0092 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-43-1908C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906767 | |||||||
| chr11:906896 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-43-2037G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906896 | |||||||
| chr11:906901 | G | C | 1 | a0002c0002t0001g0040 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-43-2042C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906901 | |||||||
| chr11:906984 | C | T | 19 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0002c0002t0001g0007 others(16): Show |
21 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.-43-2125G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906984 | |||||||
| chr11:906985 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0002c0002t0001g0212 |
3 | NA18945.hp2 NA18947.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-43-2126C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 906985 | |||||||
| chr11:907086 | A | G | 1 | a0001c0001t0001g0317 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-43-2227T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907086 | |||||||
| chr11:907206 | G | T | 9 | a0001c0001t0001g0228 a0002c0002t0001g0219 a0002c0002t0001g0220 others(6): Show |
9 | NA18952.hp1 NA18960.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.-43-2347C>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907206 | |||||||
| chr11:907400 | G | GA | 7 | a0002c0002t0001g0007 a0002c0002t0001g0087 a0002c0002t0001g0089 others(4): Show |
9 | HG00642.hp2 HG01109.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-2542dupT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907400 | |||||||
| chr11:907457 | G | C | 2 | a0001c0001t0002g0313 a0001c0001t0002g0314 |
2 | HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-43-2598C>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907457 | |||||||
| chr11:907459 | C | T | 4 | a0002c0002t0001g0223 a0002c0002t0001g0224 a0002c0002t0001g0225 others(1): Show |
4 | HG02109.hp2 HG03471.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.-43-2600G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907459 | |||||||
| chr11:907479 | TA | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
8 | HG01099.hp2 HG01167.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-2621delT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907479 | |||||||
| chr11:907510 | A | G | 1 | a0002c0002t0001g0040 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-43-2651T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907510 | |||||||
| chr11:907697 | T | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
183 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.-43-2838A>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907697 | |||||||
| chr11:907699 | C | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(144): Show |
183 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.-43-2840G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907699 | |||||||
| chr11:907792 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-43-2933G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907792 | |||||||
| chr11:907933 | G | A | 1 | a0002c0002t0001g0315 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-44+2842C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907933 | |||||||
| chr11:907936 | C | T | 2 | a0002c0002t0001g0219 a0002c0002t0001g0220 |
2 | NA18997.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-44+2839G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 907936 | |||||||
| chr11:908217 | G | A | 1 | a0002c0002t0001g0213 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-44+2558C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908217 | |||||||
| chr11:908462 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-44+2313C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908462 | |||||||
| chr11:908683 | C | T | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-44+2092G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908683 | |||||||
| chr11:908842 | C | G | 1 | a0002c0002t0001g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-44+1933G>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908842 | |||||||
| chr11:908956 | C | A | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-44+1819G>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908956 | |||||||
| chr11:908992 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG00741.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.-44+1783C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 908992 | |||||||
| chr11:909244 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-44+1531G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 909244 | |||||||
| chr11:909328 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-44+1447G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 909328 | |||||||
| chr11:909491 | G | A | 1 | a0002c0002t0001g0038 | 2 | HG01099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-44+1284C>T | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 909491 | |||||||
| chr11:909676 | T | C | 1 | a0001c0001t0007g0215 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-44+1099A>G | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 909676 | |||||||
| chr11:909947 | C | T | 2 | a0001c0001t0004g0060 a0001c0001t0004g0061 |
2 | HG01243.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-44+828G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 909947 | |||||||
| chr11:910058 | C | CA | 6 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0317 others(3): Show |
6 | HG01175.hp2 NA18991.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+716dupT | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 910058 | |||||||
| chr11:910097 | A | G | 22 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0043 others(19): Show |
24 | HG00741.hp1 HG01884.hp1 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.-44+678T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 910097 | |||||||
| chr11:910259 | A | G | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
249 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(246): Show |
intron_variant | MODIFIER | c.-44+516T>C | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 910259 | |||||||
| chr11:910558 | C | T | 1 | a0003c0003t0002g0039 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-44+217G>A | CHID1 | ENSG00000177830.18 | transcript | ENST00000323578.13 | protein_coding | 1/12 | chr11 | 910558 |