Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23309 |
| ensemblid | ENSG00000127511.10 |
| hgncid | 19354 |
| symbol | SIN3B |
| name | SIN3 transcription regulator family member B |
| refseq_nuc | NM_001297595.2 |
| refseq_prot | NP_001284524.1 |
| ensembl_nuc | ENST00000248054.10 |
| ensembl_prot | ENSP00000248054.4 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 16829398 |
| end | 16880349 |
| strand | + |
| ver | v1.2 |
| region | chr19:16829398-16880349 |
| region5000 | chr19:16824398-16885349 |
| regionname0 | SIN3B_chr19_16829398_16880349 |
| regionname5000 | SIN3B_chr19_16824398_16885349 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1130 | 362 | 89 | 75 | 154 | 12 | 30 | 119 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| a0002 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| a0003 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| a0004 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| a0005 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| a0006 | 0/0 | 1130 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| a0007 | 0/0 | 1130 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| a0008 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| a0009 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| a0010 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| a0011 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | MAHAG others(1125): Show |
chr19 | 16824398 | 16885349 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3390 | 290 | 84 | 56 | 113 | 11 | 24 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0001c0002 | 0/0 | 3390 | 50 | 0 | 4 | 39 | 1 | 6 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0001c0003 | 0/0 | 3390 | 12 | 0 | 11 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0001c0004 | 0/0 | 3390 | 4 | 4 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0001c0006 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0001c0007 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0001c0012 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0001c0014 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0001c0016 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0001c0018 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0002c0005 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0003c0011 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0004c0017 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0005c0015 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0006c0008 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0007c0020 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0008c0019 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0009c0010 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0010c0009 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 | ||
| a0011c0013 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | ATGGC others(3385): Show |
chr19 | 16824398 | 16885349 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5038 | 135 | 58 | 23 | 36 | 5 | 13 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0002 | 1/0 | 5038 | 95 | 15 | 21 | 46 | 5 | 7 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0004 | 0/0 | 5038 | 27 | 0 | 5 | 20 | 1 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0005 | 0/0 | 5038 | 14 | 1 | 4 | 6 | 0 | 3 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0006 | 0/0 | 5038 | 2 | 0 | 2 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0007 | 0/0 | 5038 | 2 | 2 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0008 | 0/0 | 5038 | 2 | 2 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0009 | 0/0 | 5038 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0010 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0011 | 0/0 | 5038 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0012 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0013 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0014 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0015 | 0/0 | 5012 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5007): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0016 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0017 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0019 | 0/0 | 5038 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0020 | 0/0 | 5038 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0021 | 0/1 | 5038 | 1 | 0 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0001t0022 | 0/0 | 5038 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0002t0003 | 0/0 | 5038 | 49 | 0 | 4 | 39 | 1 | 5 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0002t0018 | 0/0 | 5038 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0003t0002 | 0/0 | 5038 | 10 | 0 | 10 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0003t0003 | 0/0 | 5038 | 2 | 0 | 1 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0004t0002 | 0/0 | 5038 | 4 | 4 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0006t0003 | 0/0 | 5038 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0007t0003 | 0/0 | 5038 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0012t0002 | 0/0 | 5038 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0014t0001 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0016t0002 | 0/0 | 5038 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0001c0018t0002 | 0/0 | 5038 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0002c0005t0001 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0003c0011t0002 | 0/0 | 5038 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0004c0017t0001 | 0/0 | 5038 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0005c0015t0001 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0006c0008t0002 | 0/0 | 5038 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0007c0020t0002 | 0/0 | 5038 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0008c0019t0001 | 0/0 | 5038 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0009c0010t0005 | 0/0 | 5038 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0010c0009t0001 | 0/0 | 5038 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| a0011c0013t0002 | 0/0 | 5038 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | GGGGC others(5033): Show |
chr19 | 16824398 | 16885349 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0001 | 0/0 | 8 | 0 | 1 | 5 | 1 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0002 | 1/0 | 7 | 0 | 1 | 5 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0008g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0009g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0012g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0013g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0016g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0017g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0019g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0020g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0021g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0001t0022g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0002t0018g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0003t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0003t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0003t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0004t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0004t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0004t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0004t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0006t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0007t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0012t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0014t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0016t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0001c0018t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0002c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0003c0011t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0004c0017t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0005c0015t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0006c0008t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0007c0020t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0008c0019t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0009c0010t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0010c0009t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| a0011c0013t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | FIN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0229 | EUR | FIN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | FIN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | CHS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0072 | EAS | CHS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CHS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | CHS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | CHS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0173 | EAS | CHS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0227 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0262 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00733 | hp1 | a0001 | c0002 | t0003 | g0058 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00735 | hp2 | a0001 | c0001 | t0019 | g0311 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0181 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01081 | hp2 | a0001 | c0003 | t0002 | g0051 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0094 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0319 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0064 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0066 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01192 | hp2 | a0001 | c0001 | t0006 | g0093 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0174 | AMR | PUR | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0050 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0071 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0046 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0048 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01346 | hp1 | a0001 | c0016 | t0002 | g0002 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01346 | hp2 | a0001 | c0012 | t0002 | g0040 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | IBS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0011 | EUR | IBS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01884 | hp1 | a0001 | c0014 | t0001 | g0095 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01884 | hp2 | a0002 | c0005 | t0001 | g0161 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0047 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01952 | hp1 | a0001 | c0018 | t0002 | g0003 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0198 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01981 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02004 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02004 | hp2 | a0003 | c0011 | t0002 | g0017 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02015 | hp2 | a0001 | c0002 | t0003 | g0080 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0320 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02055 | hp1 | a0001 | c0001 | t0012 | g0042 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0075 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0078 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02145 | hp2 | a0001 | c0004 | t0002 | g0142 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02148 | hp2 | a0001 | c0003 | t0003 | g0053 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CDX | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | CDX | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | CDX | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02165 | hp2 | a0004 | c0017 | t0001 | g0208 | EAS | CDX | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02273 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0170 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02293 | hp2 | a0001 | c0003 | t0002 | g0052 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0049 | AMR | PEL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0068 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0321 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0176 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0122 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03139 | hp2 | a0001 | c0001 | t0014 | g0043 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03195 | hp1 | a0001 | c0004 | t0002 | g0135 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0171 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0266 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0234 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0069 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03516 | hp2 | a0001 | c0001 | t0010 | g0131 | AFR | ESN | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0140 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03704 | hp1 | a0001 | c0002 | t0018 | g0054 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03927 | hp2 | a0001 | c0002 | t0003 | g0011 | SAS | BEB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | BEB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03942 | hp2 | a0006 | c0008 | t0002 | g0168 | SAS | BEB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG04115 | hp1 | a0007 | c0020 | t0002 | g0026 | SAS | STU | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | STU | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG04184 | hp1 | a0001 | c0002 | t0003 | g0077 | SAS | BEB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | BEB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | STU | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | YRI | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0092 | EAS | CHB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | CHB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18906 | hp1 | a0008 | c0019 | t0001 | g0185 | AFR | YRI | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | YRI | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0044 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0086 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0062 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0090 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0059 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0084 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18965 | hp1 | a0009 | c0010 | t0005 | g0175 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18965 | hp2 | a0001 | c0002 | t0003 | g0089 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0061 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0056 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0018 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18997 | hp1 | a0001 | c0006 | t0003 | g0060 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18998 | hp2 | a0010 | c0009 | t0001 | g0193 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19000 | hp1 | a0001 | c0003 | t0003 | g0073 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19003 | hp2 | a0001 | c0001 | t0011 | g0190 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19007 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0180 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19030 | hp1 | a0001 | c0001 | t0007 | g0182 | AFR | LWK | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | LWK | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19055 | hp1 | a0001 | c0002 | t0003 | g0055 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19055 | hp2 | a0001 | c0001 | t0009 | g0301 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19057 | hp1 | a0001 | c0001 | t0022 | g0231 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19057 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19064 | hp2 | a0001 | c0001 | t0005 | g0177 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19066 | hp1 | a0011 | c0013 | t0002 | g0299 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19068 | hp1 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19070 | hp2 | a0001 | c0002 | t0003 | g0088 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19077 | hp2 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19078 | hp1 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19078 | hp2 | a0001 | c0001 | t0020 | g0322 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19081 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19082 | hp1 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19083 | hp1 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19085 | hp1 | a0001 | c0002 | t0003 | g0067 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0063 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19091 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0083 | EAS | JPT | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | YRI | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ASW | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA20129 | hp2 | a0001 | c0001 | t0017 | g0107 | AFR | ASW | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | TSI | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0134 | EUR | TSI | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | GIH | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0057 | SAS | GIH | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01123 | hp1 | a0001 | c0007 | t0003 | g0065 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02109 | hp1 | a0001 | c0004 | t0002 | g0143 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG02559 | hp2 | a0001 | c0004 | t0002 | g0124 | AFR | ACB | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03471 | hp1 | a0005 | c0015 | t0001 | g0109 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0163 | AFR | MSL | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | USA | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | USA | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | USA | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | LWK | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0021 | g0215 | REF | REF | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0002 | REF | REF | SIN3B_chr19_16824398_16885349 | SIN3B | chr19 | 16824398 | 16885349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16829442 | A | G | 1 | a0007 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.22A>G | p.Ser8Gly | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 1/19 | 45/5038 | 22/3393 | 8/1130 | chr19 | 16829442 | |||
| chr19:16829457 | G | T | 1 | a0008 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.37G>T | p.Ala13Ser | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 1/19 | 60/5038 | 37/3393 | 13/1130 | chr19 | 16829457 | |||
| chr19:16853108 | G | A | 1 | a0002 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.889G>A | p.Ala297Thr | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/19 | 912/5038 | 889/3393 | 297/1130 | chr19 | 16853108 | |||
| chr19:16869755 | C | T | 1 | a0005 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.2102C>T | p.Pro701Leu | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/19 | 2125/5038 | 2102/3393 | 701/1130 | chr19 | 16869755 | |||
| chr19:16876071 | G | A | 1 | a0006 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.2609G>A | p.Ser870Asn | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 15/19 | 2632/5038 | 2609/3393 | 870/1130 | chr19 | 16876071 | |||
| chr19:16876151 | C | T | 1 | a0011 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.2689C>T | p.Arg897Cys | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 15/19 | 2712/5038 | 2689/3393 | 897/1130 | chr19 | 16876151 | |||
| chr19:16878196 | T | G | 1 | a0010 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.2968T>G | p.Phe990Val | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 18/19 | 2991/5038 | 2968/3393 | 990/1130 | chr19 | 16878196 | |||
| chr19:16878346 | G | A | 1 | a0009 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.3118G>A | p.Glu1040Lys | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 18/19 | 3141/5038 | 3118/3393 | 1040/1130 | chr19 | 16878346 | |||
| chr19:16878601 | C | G | 1 | a0004 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.3267C>G | p.Asp1089Glu | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 3290/5038 | 3267/3393 | 1089/1130 | chr19 | 16878601 | |||
| chr19:16878680 | G | A | 1 | a0003 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.3346G>A | p.Val1116Met | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 3369/5038 | 3346/3393 | 1116/1130 | chr19 | 16878680 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16853125 | C | T | 1 | a0001c0018 | 1 | HG01952.hp1 | synonymous_variant | LOW | c.906C>T | p.Tyr302Tyr | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/19 | 929/5038 | 906/3393 | 302/1130 | chr19 | 16853125 | |||
| chr19:16863730 | G | A | 2 | a0001c0003 a0001c0018 |
13 | HG01081.hp2 HG01255.hp1 HG01257.hp2 others(10): Show |
synonymous_variant | LOW | c.1317G>A | p.Thr439Thr | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/19 | 1340/5038 | 1317/3393 | 439/1130 | chr19 | 16863730 | |||
| chr19:16865478 | T | C | 5 | a0001c0002 a0001c0003 a0001c0006 others(2): Show |
65 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(62): Show |
synonymous_variant | LOW | c.1452T>C | p.Ser484Ser | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/19 | 1475/5038 | 1452/3393 | 484/1130 | chr19 | 16865478 | |||
| chr19:16865517 | C | T | 1 | a0001c0004 | 4 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(1): Show |
synonymous_variant | LOW | c.1491C>T | p.Asp497Asp | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/19 | 1514/5038 | 1491/3393 | 497/1130 | chr19 | 16865517 | |||
| chr19:16866469 | C | T | 1 | a0004c0017 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.1719C>T | p.Asp573Asp | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/19 | 1742/5038 | 1719/3393 | 573/1130 | chr19 | 16866469 | |||
| chr19:16869678 | C | T | 1 | a0001c0016 | 1 | HG01346.hp1 | synonymous_variant | LOW | c.2025C>T | p.Gly675Gly | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/19 | 2048/5038 | 2025/3393 | 675/1130 | chr19 | 16869678 | |||
| chr19:16871299 | C | T | 1 | a0004c0017 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.2493C>T | p.Ile831Ile | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/19 | 2516/5038 | 2493/3393 | 831/1130 | chr19 | 16871299 | |||
| chr19:16876111 | C | T | 2 | a0001c0014 a0008c0019 |
2 | HG01884.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.2649C>T | p.Asn883Asn | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 15/19 | 2672/5038 | 2649/3393 | 883/1130 | chr19 | 16876111 | |||
| chr19:16876527 | C | T | 1 | a0001c0012 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.2808C>T | p.Ile936Ile | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 16/19 | 2831/5038 | 2808/3393 | 936/1130 | chr19 | 16876527 | |||
| chr19:16878321 | C | T | 1 | a0001c0007 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.3093C>T | p.His1031His | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 18/19 | 3116/5038 | 3093/3393 | 1031/1130 | chr19 | 16878321 | |||
| chr19:16878517 | C | T | 1 | a0001c0006 | 1 | NA18997.hp1 | synonymous_variant | LOW | c.3183C>T | p.Leu1061Leu | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 3206/5038 | 3183/3393 | 1061/1130 | chr19 | 16878517 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16878771 | C | T | 1 | a0001c0001t0008 | 2 | HG03098.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*44C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 44 | chr19 | 16878771 | ||||||
| chr19:16878853 | C | T | 1 | a0001c0001t0007 | 2 | HG02280.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*126C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 126 | chr19 | 16878853 | ||||||
| chr19:16878854 | G | A | 1 | a0001c0001t0009 | 1 | NA19055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*127G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 127 | chr19 | 16878854 | ||||||
| chr19:16878888 | C | T | 2 | a0001c0001t0004 a0001c0001t0022 |
28 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*161C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 161 | chr19 | 16878888 | ||||||
| chr19:16878936 | G | A | 1 | a0001c0001t0010 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*209G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 209 | chr19 | 16878936 | ||||||
| chr19:16879017 | G | A | 1 | a0001c0001t0007 | 2 | HG02280.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*290G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 290 | chr19 | 16879017 | ||||||
| chr19:16879059 | C | T | 1 | a0001c0001t0006 | 2 | HG01099.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*332C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 332 | chr19 | 16879059 | ||||||
| chr19:16879157 | A | G | 1 | a0001c0001t0020 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*430A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 430 | chr19 | 16879157 | ||||||
| chr19:16879163 | G | T | 1 | a0001c0001t0019 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 436 | chr19 | 16879163 | ||||||
| chr19:16879352 | G | A | 1 | a0001c0001t0010 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*625G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 625 | chr19 | 16879352 | ||||||
| chr19:16879485 | C | T | 1 | a0001c0001t0022 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*758C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 758 | chr19 | 16879485 | ||||||
| chr19:16879496 | G | A | 2 | a0001c0001t0005 a0009c0010t0005 |
15 | HG00609.hp2 HG00741.hp1 HG01109.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*769G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 769 | chr19 | 16879496 | ||||||
| chr19:16879535 | C | T | 5 | a0001c0002t0003 a0001c0002t0018 a0001c0003t0003 others(2): Show |
54 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*808C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 808 | chr19 | 16879535 | ||||||
| chr19:16879552 | C | T | 1 | a0001c0001t0017 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*825C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 825 | chr19 | 16879552 | ||||||
| chr19:16879640 | C | T | 1 | a0001c0001t0016 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*913C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 913 | chr19 | 16879640 | ||||||
| chr19:16879650 | GTCCCAGC others(19): Show |
G | 1 | a0001c0001t0015 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*927_*952delCAGCCG others(20): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 927 | INFO_REALIGN_3_PRIME | chr19 | 16879650 | |||||
| chr19:16879822 | C | T | 1 | a0001c0001t0014 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 1095 | chr19 | 16879822 | ||||||
| chr19:16879841 | A | G | 1 | a0001c0001t0013 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1114A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 1114 | chr19 | 16879841 | ||||||
| chr19:16879876 | A | G | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(17): Show |
198 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1149A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 1149 | chr19 | 16879876 | ||||||
| chr19:16879984 | T | C | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(17): Show |
195 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*1257T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 1257 | chr19 | 16879984 | ||||||
| chr19:16880045 | C | T | 1 | a0001c0002t0018 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1318C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 1318 | chr19 | 16880045 | ||||||
| chr19:16880047 | C | A | 1 | a0001c0001t0011 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1320C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 1320 | chr19 | 16880047 | ||||||
| chr19:16880055 | G | A | 1 | a0001c0001t0012 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1328G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 1328 | chr19 | 16880055 | ||||||
| chr19:16880163 | G | A | 4 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0017 others(1): Show |
32 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1436G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 19/19 | 1436 | chr19 | 16880163 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:16829558 | C | T | 1 | a0001c0001t0020g0322 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.120+18C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 1/18 | chr19 | 16829558 | |||||||
| chr19:16829586 | C | T | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.120+46C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 1/18 | chr19 | 16829586 | |||||||
| chr19:16829591 | G | T | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.120+51G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 1/18 | chr19 | 16829591 | |||||||
| chr19:16829597 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(5): Show |
9 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.120+57G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 1/18 | chr19 | 16829597 | |||||||
| chr19:16829660 | G | C | 1 | a0001c0001t0002g0034 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.120+120G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 1/18 | chr19 | 16829660 | |||||||
| chr19:16830119 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.227+222G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830119 | |||||||
| chr19:16830251 | C | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | HG01123.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.227+354C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830251 | |||||||
| chr19:16830266 | T | C | 3 | a0001c0001t0002g0039 a0001c0001t0002g0041 a0001c0012t0002g0040 |
3 | HG01346.hp2 HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.227+369T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830266 | |||||||
| chr19:16830421 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.227+524T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830421 | |||||||
| chr19:16830460 | G | T | 1 | a0001c0002t0003g0320 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.227+563G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830460 | |||||||
| chr19:16830514 | G | A | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.227+617G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830514 | |||||||
| chr19:16830534 | C | G | 1 | a0001c0001t0005g0319 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.227+637C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830534 | |||||||
| chr19:16830548 | G | A | 1 | a0001c0001t0014g0043 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.227+651G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830548 | |||||||
| chr19:16830599 | G | C | 175 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(172): Show |
201 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.227+702G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830599 | |||||||
| chr19:16830646 | T | A | 56 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0011 others(53): Show |
65 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.227+749T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830646 | |||||||
| chr19:16830788 | C | T | 3 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0004g0318 |
3 | NA18948.hp2 NA18979.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.228-706C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16830788 | |||||||
| chr19:16831053 | A | T | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.228-441A>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16831053 | |||||||
| chr19:16831064 | C | CT | 13 | a0001c0001t0001g0183 a0001c0001t0002g0184 a0001c0001t0007g0182 others(10): Show |
16 | HG02258.hp1 NA18747.hp1 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.228-414dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr19 | 16831064 | ||||||
| chr19:16831094 | G | A | 2 | a0001c0002t0003g0044 a0001c0002t0003g0045 |
2 | NA18942.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.228-400G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16831094 | |||||||
| chr19:16831114 | G | C | 1 | a0001c0001t0007g0182 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.228-380G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16831114 | |||||||
| chr19:16831155 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0312 a0001c0001t0001g0313 others(3): Show |
9 | HG00735.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.228-339C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16831155 | |||||||
| chr19:16831188 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01361.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.228-306G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16831188 | |||||||
| chr19:16831297 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.228-197A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16831297 | |||||||
| chr19:16831382 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.228-112T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 2/18 | chr19 | 16831382 | |||||||
| chr19:16831667 | C | T | 1 | a0001c0001t0004g0309 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.381+20C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16831667 | |||||||
| chr19:16831831 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.381+184C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16831831 | |||||||
| chr19:16831901 | C | T | 2 | a0001c0001t0002g0307 a0001c0001t0002g0308 |
2 | NA18747.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.381+254C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16831901 | |||||||
| chr19:16832007 | C | T | 1 | a0001c0002t0003g0083 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.381+360C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16832007 | |||||||
| chr19:16832191 | C | CT | 52 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(49): Show |
62 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.381+567dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16832191 | ||||||
| chr19:16832191 | C | CTT | 24 | a0001c0001t0002g0179 a0001c0001t0005g0171 a0001c0001t0005g0172 others(21): Show |
24 | HG00609.hp2 HG00741.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.381+566_381+567dup others(2): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16832191 | ||||||
| chr19:16832191 | CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0282 others(1): Show |
4 | HG02647.hp2 HG02809.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+556_381+567del others(12): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16832191 | ||||||
| chr19:16832191 | CTTTTTTT others(6): Show |
C | 120 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(117): Show |
133 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.381+555_381+567del others(13): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16832191 | ||||||
| chr19:16832220 | C | T | 3 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG02647.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.381+573C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16832220 | |||||||
| chr19:16832221 | G | A | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.381+574G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16832221 | |||||||
| chr19:16832445 | G | T | 1 | a0001c0001t0002g0158 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.381+798G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16832445 | |||||||
| chr19:16832490 | G | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(32): Show |
37 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.381+843G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16832490 | |||||||
| chr19:16832500 | C | CT | 8 | a0001c0001t0001g0038 a0001c0001t0001g0278 a0001c0001t0001g0279 others(5): Show |
8 | HG01099.hp2 HG01123.hp2 NA18906.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+871dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16832500 | ||||||
| chr19:16832500 | CT | C | 9 | a0001c0001t0001g0096 a0001c0001t0001g0189 a0001c0001t0002g0034 others(6): Show |
9 | HG01070.hp2 HG01168.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+871delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16832500 | ||||||
| chr19:16832689 | G | A | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.381+1042G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16832689 | |||||||
| chr19:16832709 | C | T | 1 | a0001c0001t0020g0322 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.381+1062C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16832709 | |||||||
| chr19:16832723 | C | T | 35 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(32): Show |
37 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.381+1076C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16832723 | |||||||
| chr19:16832943 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.381+1296C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16832943 | |||||||
| chr19:16833116 | G | A | 1 | a0001c0002t0003g0044 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.381+1469G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833116 | |||||||
| chr19:16833337 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.381+1690A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833337 | |||||||
| chr19:16833351 | C | T | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.381+1704C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833351 | |||||||
| chr19:16833556 | T | C | 183 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(180): Show |
198 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.381+1909T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833556 | |||||||
| chr19:16833631 | C | CA | 8 | a0001c0001t0001g0028 a0001c0001t0001g0097 a0001c0001t0001g0191 others(5): Show |
8 | HG00438.hp1 HG02074.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+1998dupA | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16833631 | ||||||
| chr19:16833710 | G | A | 4 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(1): Show |
4 | HG01255.hp2 HG01358.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+2063G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833710 | |||||||
| chr19:16833722 | G | GT | 9 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(6): Show |
9 | HG00438.hp2 HG01496.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+2085dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16833722 | ||||||
| chr19:16833733 | G | T | 127 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(124): Show |
140 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.381+2086G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833733 | |||||||
| chr19:16833759 | T | C | 1 | a0001c0001t0002g0288 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.381+2112T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833759 | |||||||
| chr19:16833835 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.381+2188T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833835 | |||||||
| chr19:16833923 | C | T | 1 | a0001c0002t0003g0072 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.381+2276C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833923 | |||||||
| chr19:16833947 | G | A | 1 | a0001c0004t0002g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+2300G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833947 | |||||||
| chr19:16833947 | G | C | 1 | a0001c0001t0019g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.381+2300G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16833947 | |||||||
| chr19:16834015 | G | A | 1 | a0001c0001t0002g0289 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.381+2368G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16834015 | |||||||
| chr19:16834155 | G | A | 1 | a0001c0002t0003g0057 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.381+2508G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16834155 | |||||||
| chr19:16834238 | A | C | 17 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(14): Show |
17 | HG00609.hp2 HG00741.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.381+2591A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16834238 | |||||||
| chr19:16834394 | G | A | 124 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(121): Show |
137 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.381+2747G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16834394 | |||||||
| chr19:16834531 | T | C | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.381+2884T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16834531 | |||||||
| chr19:16834904 | T | C | 1 | a0010c0009t0001g0193 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.381+3257T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16834904 | |||||||
| chr19:16835228 | C | CT | 6 | a0001c0001t0001g0273 a0001c0001t0002g0155 a0001c0001t0004g0272 others(3): Show |
6 | HG00639.hp1 HG01884.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+3599dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16835228 | ||||||
| chr19:16835228 | CT | C | 10 | a0001c0001t0001g0098 a0001c0001t0001g0194 a0001c0001t0001g0195 others(7): Show |
10 | HG00733.hp1 HG01169.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.381+3599delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16835228 | ||||||
| chr19:16835255 | G | C | 1 | a0001c0001t0005g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.381+3608G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16835255 | |||||||
| chr19:16835294 | T | C | 4 | a0001c0001t0002g0008 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
6 | HG00609.hp1 HG02083.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+3647T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16835294 | |||||||
| chr19:16835495 | C | CT | 31 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0159 others(28): Show |
31 | HG00609.hp2 HG00741.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.381+3865dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16835495 | ||||||
| chr19:16835495 | CT | C | 179 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(176): Show |
207 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.381+3865delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16835495 | ||||||
| chr19:16835512 | T | A | 2 | a0001c0001t0002g0290 a0001c0001t0002g0291 |
2 | HG02027.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.381+3865T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16835512 | |||||||
| chr19:16835827 | AT | A | 3 | a0001c0001t0001g0273 a0001c0001t0002g0128 a0001c0001t0002g0305 |
3 | NA18968.hp1 NA19003.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.381+4185delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16835827 | ||||||
| chr19:16835837 | C | T | 128 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(125): Show |
141 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.381+4190C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16835837 | |||||||
| chr19:16835953 | T | C | 241 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(238): Show |
265 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.381+4306T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16835953 | |||||||
| chr19:16835993 | T | C | 56 | a0001c0001t0002g0129 a0001c0002t0003g0004 a0001c0002t0003g0007 others(53): Show |
65 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.381+4346T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16835993 | |||||||
| chr19:16835995 | C | A | 1 | a0001c0002t0003g0011 | 2 | HG01516.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.381+4348C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16835995 | |||||||
| chr19:16835995 | C | T | 1 | a0001c0002t0003g0070 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.381+4348C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16835995 | |||||||
| chr19:16836000 | C | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0312 a0001c0001t0001g0313 others(2): Show |
8 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+4353C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836000 | |||||||
| chr19:16836038 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.381+4391G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836038 | |||||||
| chr19:16836261 | T | G | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.381+4614T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836261 | |||||||
| chr19:16836316 | C | T | 1 | a0001c0002t0003g0069 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.381+4669C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836316 | |||||||
| chr19:16836319 | G | A | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.381+4672G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836319 | |||||||
| chr19:16836335 | C | T | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.381+4688C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836335 | |||||||
| chr19:16836382 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.381+4735C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836382 | |||||||
| chr19:16836552 | T | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0184 |
2 | NA19005.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.381+4905T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836552 | |||||||
| chr19:16836628 | A | G | 4 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0008g0122 others(1): Show |
4 | HG02258.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+4981A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836628 | |||||||
| chr19:16836837 | C | A | 6 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(3): Show |
6 | HG01496.hp1 HG01975.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-4931C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836837 | |||||||
| chr19:16836880 | G | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0274 |
3 | HG01358.hp2 HG01981.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.382-4888G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836880 | |||||||
| chr19:16836969 | T | C | 297 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(294): Show |
336 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(333): Show |
intron_variant | MODIFIER | c.382-4799T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16836969 | |||||||
| chr19:16837003 | G | T | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.382-4765G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837003 | |||||||
| chr19:16837030 | T | A | 1 | a0004c0017t0001g0208 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.382-4738T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837030 | |||||||
| chr19:16837238 | G | A | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.382-4530G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837238 | |||||||
| chr19:16837261 | G | A | 1 | a0001c0002t0003g0081 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.382-4507G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837261 | |||||||
| chr19:16837438 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.382-4330C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837438 | |||||||
| chr19:16837441 | T | C | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.382-4327T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837441 | |||||||
| chr19:16837469 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.382-4299G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837469 | |||||||
| chr19:16837706 | G | T | 1 | a0001c0001t0002g0303 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.382-4062G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837706 | |||||||
| chr19:16837769 | G | T | 1 | a0001c0001t0001g0267 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.382-3999G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837769 | |||||||
| chr19:16837772 | C | T | 1 | a0002c0005t0001g0161 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.382-3996C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837772 | |||||||
| chr19:16837873 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0004g0209 |
2 | HG00423.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.382-3895T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837873 | |||||||
| chr19:16837937 | C | T | 1 | a0004c0017t0001g0208 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.382-3831C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16837937 | |||||||
| chr19:16838058 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 |
3 | HG01123.hp2 HG02970.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.382-3710C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16838058 | |||||||
| chr19:16838194 | A | T | 56 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0011 others(53): Show |
65 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.382-3574A>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16838194 | |||||||
| chr19:16838233 | AATC | A | 35 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(32): Show |
37 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.382-3526_382-3524d others(5): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16838233 | ||||||
| chr19:16838481 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.382-3287G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16838481 | |||||||
| chr19:16838634 | G | A | 1 | a0001c0002t0018g0054 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.382-3134G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16838634 | |||||||
| chr19:16838756 | C | G | 1 | a0001c0001t0001g0276 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.382-3012C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16838756 | |||||||
| chr19:16838800 | T | C | 2 | a0001c0002t0003g0012 a0001c0002t0003g0055 |
3 | NA19055.hp1 NA19060.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.382-2968T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16838800 | |||||||
| chr19:16838828 | C | T | 47 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0011 others(44): Show |
54 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.382-2940C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16838828 | |||||||
| chr19:16838871 | A | G | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.382-2897A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16838871 | |||||||
| chr19:16838898 | T | A | 1 | a0001c0001t0001g0212 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.382-2870T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16838898 | |||||||
| chr19:16838921 | C | T | 1 | a0001c0001t0005g0266 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.382-2847C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16838921 | |||||||
| chr19:16838970 | C | CT | 158 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(155): Show |
173 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.382-2778dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16838970 | ||||||
| chr19:16838970 | C | CTT | 17 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(14): Show |
17 | HG00423.hp2 HG01109.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.382-2779_382-2778d others(4): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr19 | 16838970 | ||||||
| chr19:16839079 | C | T | 1 | a0001c0001t0004g0262 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.382-2689C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839079 | |||||||
| chr19:16839154 | G | C | 124 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(121): Show |
137 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.382-2614G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839154 | |||||||
| chr19:16839157 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.382-2611G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839157 | |||||||
| chr19:16839376 | G | C | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.382-2392G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839376 | |||||||
| chr19:16839413 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0192 |
3 | HG02976.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.382-2355C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839413 | |||||||
| chr19:16839453 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.382-2315G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839453 | |||||||
| chr19:16839544 | C | T | 1 | a0001c0001t0005g0181 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.382-2224C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839544 | |||||||
| chr19:16839666 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.382-2102G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839666 | |||||||
| chr19:16839706 | T | G | 1 | a0001c0001t0001g0213 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.382-2062T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839706 | |||||||
| chr19:16839733 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.382-2035G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839733 | |||||||
| chr19:16839801 | A | T | 1 | a0001c0002t0018g0054 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.382-1967A>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839801 | |||||||
| chr19:16839842 | C | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG01361.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.382-1926C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839842 | |||||||
| chr19:16839882 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.382-1886C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839882 | |||||||
| chr19:16839883 | G | A | 1 | a0001c0001t0010g0131 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.382-1885G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839883 | |||||||
| chr19:16839952 | C | T | 47 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0011 others(44): Show |
54 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.382-1816C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16839952 | |||||||
| chr19:16840010 | A | G | 47 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0011 others(44): Show |
54 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.382-1758A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16840010 | |||||||
| chr19:16840095 | A | G | 3 | a0001c0002t0003g0012 a0001c0002t0003g0055 a0001c0002t0003g0056 |
4 | NA18986.hp1 NA19055.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-1673A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16840095 | |||||||
| chr19:16840266 | A | G | 140 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(137): Show |
153 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.382-1502A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16840266 | |||||||
| chr19:16840362 | C | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(117): Show |
132 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.382-1406C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16840362 | |||||||
| chr19:16840377 | C | T | 3 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02109.hp2 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.382-1391C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16840377 | |||||||
| chr19:16840757 | C | T | 1 | a0001c0002t0003g0058 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.382-1011C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16840757 | |||||||
| chr19:16840883 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.382-885C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16840883 | |||||||
| chr19:16840893 | A | C | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.382-875A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16840893 | |||||||
| chr19:16841078 | T | C | 13 | a0001c0001t0002g0179 a0001c0001t0005g0123 a0001c0001t0005g0171 others(10): Show |
13 | HG00609.hp2 HG00741.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.382-690T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16841078 | |||||||
| chr19:16841151 | G | A | 1 | a0001c0002t0003g0076 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.382-617G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16841151 | |||||||
| chr19:16841287 | C | T | 3 | a0001c0001t0002g0151 a0001c0001t0002g0152 a0006c0008t0002g0168 |
3 | HG02602.hp1 HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.382-481C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16841287 | |||||||
| chr19:16841319 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.382-449G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16841319 | |||||||
| chr19:16841348 | C | A | 1 | a0001c0001t0005g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.382-420C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16841348 | |||||||
| chr19:16841378 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.382-390G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16841378 | |||||||
| chr19:16841717 | C | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.382-51C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16841717 | |||||||
| chr19:16841726 | T | A | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.382-42T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 3/18 | chr19 | 16841726 | |||||||
| chr19:16842171 | T | A | 2 | a0001c0001t0007g0170 a0001c0001t0007g0182 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.582+203T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16842171 | |||||||
| chr19:16842405 | C | CT | 26 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0101 others(23): Show |
26 | HG01071.hp1 HG01099.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.582+456dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16842405 | ||||||
| chr19:16842509 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.582+541C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16842509 | |||||||
| chr19:16842606 | C | T | 19 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(16): Show |
19 | HG01070.hp2 HG01071.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.582+638C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16842606 | |||||||
| chr19:16842802 | G | A | 4 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0001t0002g0286 others(1): Show |
4 | HG01255.hp2 HG01358.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.582+834G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16842802 | |||||||
| chr19:16842955 | G | A | 1 | a0001c0001t0005g0319 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.582+987G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16842955 | |||||||
| chr19:16843009 | G | A | 1 | a0001c0001t0002g0306 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.582+1041G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843009 | |||||||
| chr19:16843043 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.582+1075C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843043 | |||||||
| chr19:16843069 | G | A | 195 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(192): Show |
212 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.582+1101G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843069 | |||||||
| chr19:16843387 | C | G | 1 | a0001c0001t0001g0199 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.582+1419C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843387 | |||||||
| chr19:16843407 | G | C | 2 | a0001c0001t0006g0093 a0001c0001t0006g0094 |
2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.582+1439G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843407 | |||||||
| chr19:16843463 | C | T | 1 | a0001c0002t0003g0068 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.582+1495C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843463 | |||||||
| chr19:16843721 | A | G | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.582+1753A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843721 | |||||||
| chr19:16843830 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.582+1862C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843830 | |||||||
| chr19:16843840 | A | G | 1 | a0001c0001t0002g0302 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.582+1872A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843840 | |||||||
| chr19:16843847 | CT | C | 231 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(228): Show |
253 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.582+1886delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16843847 | ||||||
| chr19:16843852 | T | G | 233 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(230): Show |
255 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.582+1884T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843852 | |||||||
| chr19:16843853 | T | C | 233 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(230): Show |
255 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.582+1885T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843853 | |||||||
| chr19:16843861 | AT | A | 233 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(230): Show |
255 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.582+1900delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr19 | 16843861 | ||||||
| chr19:16843990 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.582+2022C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843990 | |||||||
| chr19:16843995 | G | A | 120 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(117): Show |
132 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.582+2027G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16843995 | |||||||
| chr19:16844007 | G | A | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.582+2039G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16844007 | |||||||
| chr19:16844730 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.583-2240G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16844730 | |||||||
| chr19:16844732 | G | A | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.583-2238G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16844732 | |||||||
| chr19:16844764 | C | T | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.583-2206C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16844764 | |||||||
| chr19:16844923 | C | T | 4 | a0001c0001t0002g0121 a0001c0001t0002g0144 a0001c0001t0002g0145 others(1): Show |
4 | HG00280.hp1 HG01168.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-2047C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16844923 | |||||||
| chr19:16845183 | C | G | 2 | a0001c0001t0004g0024 a0001c0001t0004g0272 |
3 | NA18947.hp2 NA18968.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.583-1787C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16845183 | |||||||
| chr19:16845223 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0192 a0001c0001t0001g0257 |
4 | HG02976.hp2 NA18522.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.583-1747A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16845223 | |||||||
| chr19:16845421 | C | T | 1 | a0001c0001t0004g0262 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.583-1549C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16845421 | |||||||
| chr19:16845458 | A | T | 1 | a0001c0001t0014g0043 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.583-1512A>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16845458 | |||||||
| chr19:16845553 | C | G | 127 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(124): Show |
140 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.583-1417C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16845553 | |||||||
| chr19:16845562 | C | T | 1 | a0001c0001t0005g0123 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.583-1408C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16845562 | |||||||
| chr19:16845765 | G | A | 2 | a0001c0001t0004g0024 a0001c0001t0004g0272 |
3 | NA18947.hp2 NA18968.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.583-1205G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16845765 | |||||||
| chr19:16845921 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.583-1049G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16845921 | |||||||
| chr19:16845962 | A | G | 1 | a0001c0001t0019g0311 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.583-1008A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16845962 | |||||||
| chr19:16846024 | C | T | 1 | a0001c0004t0002g0143 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.583-946C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16846024 | |||||||
| chr19:16846055 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0103 |
3 | HG01081.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.583-915G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16846055 | |||||||
| chr19:16846327 | A | C | 1 | a0001c0002t0003g0063 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.583-643A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16846327 | |||||||
| chr19:16846469 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.583-501C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16846469 | |||||||
| chr19:16846787 | A | G | 12 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.583-183A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16846787 | |||||||
| chr19:16846827 | A | C | 144 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(141): Show |
157 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.583-143A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16846827 | |||||||
| chr19:16846837 | C | T | 1 | a0001c0001t0006g0094 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.583-133C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 4/18 | chr19 | 16846837 | |||||||
| chr19:16847145 | G | C | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.726+32G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16847145 | |||||||
| chr19:16847160 | C | T | 2 | a0001c0001t0007g0170 a0001c0001t0007g0182 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.726+47C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16847160 | |||||||
| chr19:16847263 | G | A | 1 | a0001c0002t0003g0058 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.726+150G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16847263 | |||||||
| chr19:16847352 | T | C | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.726+239T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16847352 | |||||||
| chr19:16847487 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.726+374A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16847487 | |||||||
| chr19:16847493 | G | A | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.726+380G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16847493 | |||||||
| chr19:16847495 | T | C | 4 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0008g0122 others(1): Show |
4 | HG02258.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+382T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16847495 | |||||||
| chr19:16847694 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.726+581G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16847694 | |||||||
| chr19:16847719 | C | G | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.726+606C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16847719 | |||||||
| chr19:16847756 | G | T | 1 | a0001c0002t0003g0084 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.726+643G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16847756 | |||||||
| chr19:16848057 | T | C | 184 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(181): Show |
199 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.726+944T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848057 | |||||||
| chr19:16848144 | C | T | 44 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(41): Show |
46 | HG00609.hp2 HG00741.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.726+1031C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848144 | |||||||
| chr19:16848164 | T | G | 3 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02109.hp2 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.726+1051T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848164 | |||||||
| chr19:16848183 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.726+1070T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848183 | |||||||
| chr19:16848236 | C | T | 1 | a0001c0001t0006g0093 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.726+1123C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848236 | |||||||
| chr19:16848372 | A | G | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.726+1259A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848372 | |||||||
| chr19:16848400 | G | C | 242 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(239): Show |
266 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.726+1287G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848400 | |||||||
| chr19:16848426 | G | GT | 21 | a0001c0001t0001g0213 a0001c0001t0001g0255 a0001c0001t0002g0117 others(18): Show |
21 | HG00735.hp1 HG01109.hp2 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.726+1332dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16848426 | ||||||
| chr19:16848426 | GT | G | 22 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(19): Show |
22 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.726+1332delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16848426 | ||||||
| chr19:16848426 | GTT | G | 14 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(11): Show |
15 | HG02055.hp2 HG02145.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.726+1331_726+1332d others(4): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16848426 | ||||||
| chr19:16848446 | G | T | 1 | a0001c0001t0005g0180 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.726+1333G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848446 | |||||||
| chr19:16848474 | G | A | 2 | a0001c0001t0002g0125 a0001c0001t0002g0126 |
2 | HG00609.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.726+1361G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848474 | |||||||
| chr19:16848655 | G | A | 2 | a0001c0001t0007g0170 a0001c0001t0007g0182 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.726+1542G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848655 | |||||||
| chr19:16848720 | C | T | 1 | a0001c0001t0004g0254 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.726+1607C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848720 | |||||||
| chr19:16848738 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.726+1625C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848738 | |||||||
| chr19:16848796 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0103 a0001c0001t0001g0105 |
4 | HG01081.hp1 HG02809.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.726+1683C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848796 | |||||||
| chr19:16848797 | G | A | 1 | a0001c0001t0005g0173 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.726+1684G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848797 | |||||||
| chr19:16848882 | C | T | 1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.726+1769C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16848882 | |||||||
| chr19:16849074 | A | T | 1 | a0001c0001t0002g0034 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.726+1961A>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849074 | |||||||
| chr19:16849245 | G | A | 124 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(121): Show |
137 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.726+2132G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849245 | |||||||
| chr19:16849366 | A | G | 1 | a0001c0001t0001g0013 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.727-2046A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849366 | |||||||
| chr19:16849395 | CACTTTAT others(36): Show |
C | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.727-1993_727-1951d others(45): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16849395 | ||||||
| chr19:16849418 | G | T | 1 | a0001c0001t0002g0034 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.727-1994G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849418 | |||||||
| chr19:16849521 | A | T | 1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.727-1891A>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849521 | |||||||
| chr19:16849660 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0016g0321 |
2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.727-1752A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849660 | |||||||
| chr19:16849753 | G | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0108 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.727-1659G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849753 | |||||||
| chr19:16849789 | T | C | 1 | a0001c0001t0005g0198 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.727-1623T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849789 | |||||||
| chr19:16849820 | G | T | 1 | a0001c0001t0001g0192 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.727-1592G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849820 | |||||||
| chr19:16849824 | C | T | 13 | a0001c0001t0002g0179 a0001c0001t0005g0123 a0001c0001t0005g0171 others(10): Show |
13 | HG00609.hp2 HG00741.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.727-1588C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849824 | |||||||
| chr19:16849848 | T | C | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.727-1564T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849848 | |||||||
| chr19:16849859 | A | G | 143 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(140): Show |
156 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.727-1553A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849859 | |||||||
| chr19:16849887 | C | T | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.727-1525C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849887 | |||||||
| chr19:16849915 | C | T | 1 | a0001c0001t0005g0181 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.727-1497C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16849915 | |||||||
| chr19:16849956 | C | CA | 10 | a0001c0001t0001g0217 a0001c0001t0001g0255 a0001c0001t0001g0257 others(7): Show |
10 | HG02074.hp2 HG02145.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.727-1439dupA | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16849956 | ||||||
| chr19:16850060 | C | A | 1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.727-1352C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850060 | |||||||
| chr19:16850240 | T | A | 1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.727-1172T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850240 | |||||||
| chr19:16850301 | A | C | 1 | a0001c0002t0003g0070 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.727-1111A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850301 | |||||||
| chr19:16850307 | T | C | 1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.727-1105T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850307 | |||||||
| chr19:16850308 | C | T | 1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.727-1104C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850308 | |||||||
| chr19:16850380 | C | G | 1 | a0001c0001t0002g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.727-1032C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850380 | |||||||
| chr19:16850391 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.727-1021G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850391 | |||||||
| chr19:16850606 | G | C | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.727-806G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850606 | |||||||
| chr19:16850649 | C | T | 1 | a0001c0002t0003g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.727-763C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850649 | |||||||
| chr19:16850817 | C | T | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.727-595C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850817 | |||||||
| chr19:16850874 | A | T | 1 | a0001c0001t0002g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.727-538A>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850874 | |||||||
| chr19:16850912 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.727-500G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850912 | |||||||
| chr19:16850960 | A | G | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.727-452A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850960 | |||||||
| chr19:16850961 | C | A | 1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.727-451C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850961 | |||||||
| chr19:16850962 | CT | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(116): Show |
131 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.727-449delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850962 | |||||||
| chr19:16850963 | T | C | 1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.727-449T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16850963 | |||||||
| chr19:16851058 | C | T | 183 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(180): Show |
198 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.727-354C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16851058 | |||||||
| chr19:16851088 | T | TG | 243 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(240): Show |
267 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.727-322dupG | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16851088 | ||||||
| chr19:16851206 | G | C | 1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.727-206G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16851206 | |||||||
| chr19:16851217 | CTG | C | 4 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0264 others(1): Show |
4 | HG01109.hp1 HG02451.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-192_727-191del others(2): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr19 | 16851217 | ||||||
| chr19:16851314 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.727-98C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16851314 | |||||||
| chr19:16851372 | C | G | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.727-40C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16851372 | |||||||
| chr19:16851381 | G | A | 4 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0008g0122 others(1): Show |
4 | HG02258.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.727-31G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 5/18 | chr19 | 16851381 | |||||||
| chr19:16851574 | C | A | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.849+40C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16851574 | |||||||
| chr19:16851616 | G | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(4): Show |
8 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.849+82G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16851616 | |||||||
| chr19:16851672 | T | G | 1 | a0001c0001t0002g0034 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.849+138T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16851672 | |||||||
| chr19:16851747 | A | G | 1 | a0001c0002t0003g0067 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.849+213A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16851747 | |||||||
| chr19:16851819 | T | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0104 |
2 | HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.849+285T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16851819 | |||||||
| chr19:16851829 | G | T | 1 | a0001c0001t0002g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.849+295G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16851829 | |||||||
| chr19:16851866 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.849+332C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16851866 | |||||||
| chr19:16852195 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.849+661C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852195 | |||||||
| chr19:16852439 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.850-630G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852439 | |||||||
| chr19:16852443 | C | T | 1 | a0001c0001t0002g0305 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.850-626C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852443 | |||||||
| chr19:16852447 | G | A | 146 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(143): Show |
159 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.850-622G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852447 | |||||||
| chr19:16852521 | A | G | 31 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(28): Show |
33 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.850-548A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852521 | |||||||
| chr19:16852608 | A | G | 2 | a0001c0001t0002g0292 a0011c0013t0002g0299 |
2 | NA18946.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.850-461A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852608 | |||||||
| chr19:16852642 | C | A | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.850-427C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852642 | |||||||
| chr19:16852744 | G | A | 13 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0004g0018 others(10): Show |
15 | NA18940.hp1 NA18947.hp2 NA18948.hp1 others(12): Show |
intron_variant | MODIFIER | c.850-325G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852744 | |||||||
| chr19:16852843 | C | G | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.850-226C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852843 | |||||||
| chr19:16852923 | C | T | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.850-146C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852923 | |||||||
| chr19:16852978 | G | A | 1 | a0001c0001t0002g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.850-91G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 6/18 | chr19 | 16852978 | |||||||
| chr19:16853284 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.939+126C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/18 | chr19 | 16853284 | |||||||
| chr19:16853360 | G | C | 2 | a0001c0001t0007g0170 a0001c0001t0007g0182 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.939+202G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/18 | chr19 | 16853360 | |||||||
| chr19:16853564 | A | G | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.939+406A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/18 | chr19 | 16853564 | |||||||
| chr19:16853574 | C | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0270 others(1): Show |
6 | HG02071.hp2 HG02129.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+416C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/18 | chr19 | 16853574 | |||||||
| chr19:16853656 | T | C | 1 | a0001c0001t0002g0118 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.940-487T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/18 | chr19 | 16853656 | |||||||
| chr19:16853694 | C | T | 1 | a0001c0002t0003g0058 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.940-449C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/18 | chr19 | 16853694 | |||||||
| chr19:16853715 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.940-428G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/18 | chr19 | 16853715 | |||||||
| chr19:16853785 | C | T | 1 | a0001c0003t0002g0051 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.940-358C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/18 | chr19 | 16853785 | |||||||
| chr19:16853802 | CTG | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0098 a0001c0001t0001g0104 others(4): Show |
8 | HG02056.hp1 HG02074.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.940-338_940-337del others(2): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr19 | 16853802 | ||||||
| chr19:16853987 | C | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0150 a0001c0001t0002g0157 |
4 | HG02257.hp2 HG02280.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.940-156C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 7/18 | chr19 | 16853987 | |||||||
| chr19:16854587 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1058+326A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16854587 | |||||||
| chr19:16854957 | G | A | 4 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0008g0122 others(1): Show |
4 | HG02258.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+696G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16854957 | |||||||
| chr19:16854971 | C | T | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1058+710C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16854971 | |||||||
| chr19:16855083 | A | G | 4 | a0001c0001t0002g0008 a0001c0001t0002g0125 a0001c0001t0002g0126 others(1): Show |
6 | HG00609.hp1 HG02083.hp1 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+822A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855083 | |||||||
| chr19:16855210 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0104 |
2 | HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1058+949C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855210 | |||||||
| chr19:16855270 | C | T | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1058+1009C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855270 | |||||||
| chr19:16855274 | C | A | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1058+1013C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855274 | |||||||
| chr19:16855370 | T | C | 3 | a0001c0001t0005g0174 a0001c0001t0005g0181 a0001c0001t0016g0321 |
3 | HG00741.hp1 HG01243.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1058+1109T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855370 | |||||||
| chr19:16855370 | T | TC | 45 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0031 others(42): Show |
48 | HG00408.hp2 HG00438.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.1058+1124dupC | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16855370 | ||||||
| chr19:16855370 | T | TCC | 21 | a0001c0001t0001g0037 a0001c0001t0001g0188 a0001c0001t0001g0213 others(18): Show |
21 | HG01192.hp2 HG01255.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.1058+1123_1058+112 others(6): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16855370 | ||||||
| chr19:16855370 | T | TCCC | 45 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(42): Show |
49 | HG00423.hp2 HG00609.hp2 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.1058+1122_1058+112 others(7): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16855370 | ||||||
| chr19:16855370 | T | TCCCC | 40 | a0001c0001t0001g0020 a0001c0001t0001g0187 a0001c0001t0001g0191 others(37): Show |
42 | HG00438.hp1 HG00558.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.1058+1121_1058+112 others(8): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16855370 | ||||||
| chr19:16855370 | TC | T | 21 | a0001c0001t0001g0013 a0001c0001t0001g0029 a0001c0001t0001g0099 others(18): Show |
24 | HG01081.hp1 HG01943.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1058+1124delC | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16855370 | ||||||
| chr19:16855370 | TCC | T | 52 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0108 others(49): Show |
59 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.1058+1123_1058+112 others(6): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16855370 | ||||||
| chr19:16855378 | C | A | 1 | a0001c0001t0001g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1058+1117C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855378 | |||||||
| chr19:16855379 | C | G | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1058+1118C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855379 | |||||||
| chr19:16855380 | C | A | 47 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0011 others(44): Show |
54 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1058+1119C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855380 | |||||||
| chr19:16855380 | C | CA | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1058+1119_1058+112 others(5): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855380 | |||||||
| chr19:16855380 | C | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0192 |
3 | HG02976.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1058+1119C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855380 | |||||||
| chr19:16855382 | C | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 |
3 | HG02258.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1058+1121C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855382 | |||||||
| chr19:16855486 | C | T | 2 | a0001c0001t0006g0093 a0001c0001t0006g0094 |
2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1058+1225C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855486 | |||||||
| chr19:16855559 | A | G | 1 | a0001c0001t0002g0305 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1058+1298A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855559 | |||||||
| chr19:16855578 | G | A | 3 | a0001c0001t0001g0097 a0001c0001t0001g0111 a0001c0001t0001g0112 |
3 | HG02109.hp2 HG02486.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1058+1317G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855578 | |||||||
| chr19:16855687 | C | T | 6 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0139 others(3): Show |
9 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1058+1426C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855687 | |||||||
| chr19:16855783 | C | T | 47 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0011 others(44): Show |
54 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1058+1522C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16855783 | |||||||
| chr19:16856034 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1058+1773G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16856034 | |||||||
| chr19:16856335 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1058+2074G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16856335 | |||||||
| chr19:16856396 | C | T | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1058+2135C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16856396 | |||||||
| chr19:16856397 | G | A | 1 | a0001c0001t0004g0224 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1058+2136G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16856397 | |||||||
| chr19:16856587 | T | C | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1058+2326T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16856587 | |||||||
| chr19:16856634 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1058+2373C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16856634 | |||||||
| chr19:16856798 | C | G | 2 | a0001c0001t0001g0210 a0001c0001t0004g0209 |
2 | HG00423.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1058+2537C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16856798 | |||||||
| chr19:16856927 | C | T | 106 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(103): Show |
115 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1058+2666C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16856927 | |||||||
| chr19:16857005 | C | T | 3 | a0001c0001t0002g0039 a0001c0001t0002g0041 a0001c0012t0002g0040 |
3 | HG01346.hp2 HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1058+2744C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857005 | |||||||
| chr19:16857029 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1058+2768A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857029 | |||||||
| chr19:16857198 | A | G | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1058+2937A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857198 | |||||||
| chr19:16857512 | AAAATATG others(5): Show |
A | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1058+3252_1058+326 others(16): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857512 | |||||||
| chr19:16857514 | A | ATATGTGT others(6): Show |
1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1058+3253_1058+325 others(17): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857514 | |||||||
| chr19:16857515 | A | G | 1 | a0001c0001t0004g0216 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1058+3254A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857515 | |||||||
| chr19:16857517 | A | ATG | 8 | a0001c0001t0001g0013 a0001c0001t0001g0103 a0001c0001t0002g0002 others(5): Show |
9 | HG01081.hp1 HG01346.hp1 HG03490.hp1 others(6): Show |
intron_variant | MODIFIER | c.1058+3292_1058+329 others(6): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857517 | A | ATGTGTG | 12 | a0001c0001t0001g0025 a0001c0001t0001g0033 a0001c0001t0001g0098 others(9): Show |
12 | HG01256.hp2 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1058+3288_1058+329 others(10): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857517 | A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0110 others(2): Show |
5 | HG02148.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+3286_1058+329 others(12): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857517 | A | ATGTGTGT others(3): Show |
11 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0027 others(8): Show |
12 | HG01168.hp2 HG01169.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1058+3284_1058+329 others(14): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857517 | A | ATGTGTGT others(5): Show |
4 | a0001c0001t0001g0236 a0001c0001t0001g0244 a0001c0001t0004g0024 others(1): Show |
5 | HG02895.hp1 HG02897.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+3282_1058+329 others(16): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857517 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0283 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1058+3280_1058+329 others(18): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857517 | A | ATGTGTGT others(9): Show |
5 | a0001c0001t0001g0199 a0001c0001t0001g0214 a0001c0001t0001g0251 others(2): Show |
5 | HG00558.hp2 HG02300.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+3278_1058+329 others(20): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857517 | A | ATGTGTGT others(11): Show |
2 | a0001c0001t0001g0023 a0001c0001t0001g0217 |
2 | HG02071.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1058+3276_1058+329 others(22): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857517 | A | G | 2 | a0001c0001t0004g0216 a0001c0006t0003g0060 |
2 | NA18946.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1058+3256A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857517 | |||||||
| chr19:16857517 | ATG | A | 29 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(26): Show |
30 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.1058+3292_1058+329 others(6): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857517 | ATGTG | A | 3 | a0001c0001t0002g0016 a0001c0001t0002g0150 a0001c0001t0002g0165 |
4 | HG02257.hp2 HG02486.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+3290_1058+329 others(8): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857517 | ATGTGTGT others(5): Show |
A | 1 | a0001c0007t0003g0065 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1058+3282_1058+329 others(16): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857517 | ||||||
| chr19:16857553 | G | A | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0006t0003g0060 others(1): Show |
4 | HG01884.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+3292G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857553 | |||||||
| chr19:16857553 | G | GTGTA | 4 | a0001c0001t0001g0006 a0001c0001t0001g0267 a0001c0002t0003g0044 others(1): Show |
4 | HG03453.hp1 NA18942.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+3293_1058+329 others(8): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTA | 41 | a0001c0001t0001g0006 a0001c0001t0001g0097 a0001c0001t0001g0099 others(38): Show |
47 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1058+3293_1058+329 others(10): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTAT others(1): Show |
4 | a0001c0002t0003g0012 a0001c0002t0003g0055 a0001c0002t0003g0056 others(1): Show |
5 | NA18906.hp1 NA18986.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+3293_1058+329 others(12): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(1): Show |
11 | a0001c0001t0001g0096 a0001c0001t0001g0108 a0001c0001t0001g0250 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.1058+3293_1058+329 others(12): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(3): Show |
12 | a0001c0001t0001g0006 a0001c0001t0001g0101 a0001c0001t0001g0189 others(9): Show |
12 | HG01496.hp2 HG02055.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.1058+3293_1058+329 others(14): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(5): Show |
16 | a0001c0001t0001g0019 a0001c0001t0001g0102 a0001c0001t0001g0186 others(13): Show |
17 | HG01358.hp2 HG01433.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.1058+3293_1058+329 others(16): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(7): Show |
2 | a0001c0001t0001g0226 a0001c0001t0002g0120 |
2 | NA18987.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1058+3293_1058+329 others(18): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(7): Show |
36 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0191 others(33): Show |
36 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.1058+3293_1058+329 others(18): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(9): Show |
1 | a0001c0001t0001g0275 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1058+3293_1058+329 others(20): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(9): Show |
30 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(27): Show |
32 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1058+3293_1058+329 others(20): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(11): Show |
1 | a0001c0001t0004g0220 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1058+3293_1058+329 others(22): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(15): Show |
1 | a0001c0001t0001g0259 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1058+3293_1058+329 others(26): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(11): Show |
7 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0245 others(4): Show |
7 | HG00735.hp2 HG02040.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1058+3293_1058+329 others(22): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857553 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0235 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1058+3293_1058+329 others(24): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857553 | ||||||
| chr19:16857555 | A | G | 23 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0027 others(20): Show |
25 | HG01261.hp2 HG02055.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.1058+3294A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857555 | |||||||
| chr19:16857557 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0192 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1058+3296A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857557 | |||||||
| chr19:16857579 | AATGTAAA others(23): Show |
A | 1 | a0001c0001t0002g0293 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1058+3320_1058+334 others(34): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857579 | ||||||
| chr19:16857581 | T | C | 3 | a0001c0002t0003g0088 a0001c0002t0003g0089 a0001c0002t0003g0091 |
3 | NA18965.hp2 NA19062.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1058+3320T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857581 | |||||||
| chr19:16857852 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1058+3591C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857852 | |||||||
| chr19:16857865 | CTCTTTTC others(3): Show |
C | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG01074.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1058+3621_1058+363 others(14): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16857865 | ||||||
| chr19:16857870 | T | C | 1 | a0001c0001t0002g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1058+3609T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16857870 | |||||||
| chr19:16858132 | C | G | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1058+3871C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858132 | |||||||
| chr19:16858204 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0314 |
5 | HG02257.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+3943G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858204 | |||||||
| chr19:16858384 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0104 |
2 | HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1059-3968C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858384 | |||||||
| chr19:16858428 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1059-3924G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858428 | |||||||
| chr19:16858554 | C | T | 52 | a0001c0001t0002g0016 a0001c0001t0002g0150 a0001c0001t0002g0157 others(49): Show |
60 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.1059-3798C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858554 | |||||||
| chr19:16858588 | G | A | 88 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(85): Show |
98 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.1059-3764G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858588 | |||||||
| chr19:16858687 | C | T | 9 | a0001c0003t0002g0003 a0001c0003t0002g0046 a0001c0003t0002g0047 others(6): Show |
11 | HG01081.hp2 HG01255.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1059-3665C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858687 | |||||||
| chr19:16858882 | A | C | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-3470A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858882 | |||||||
| chr19:16858913 | G | A | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059-3439G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858913 | |||||||
| chr19:16858946 | C | CA | 5 | a0001c0001t0001g0101 a0001c0001t0001g0226 a0001c0001t0002g0133 others(2): Show |
5 | HG02055.hp2 HG02602.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059-3399dupA | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16858946 | ||||||
| chr19:16858946 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1059-3406C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858946 | |||||||
| chr19:16858951 | A | C | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-3401A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858951 | |||||||
| chr19:16858979 | T | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0104 a0001c0001t0001g0106 |
3 | HG02896.hp2 HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1059-3373T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16858979 | |||||||
| chr19:16859044 | T | C | 52 | a0001c0001t0002g0016 a0001c0001t0002g0150 a0001c0001t0002g0157 others(49): Show |
60 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.1059-3308T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16859044 | |||||||
| chr19:16859867 | A | G | 2 | a0001c0001t0007g0170 a0001c0001t0007g0182 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1059-2485A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16859867 | |||||||
| chr19:16859976 | A | C | 1 | a0001c0001t0009g0301 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1059-2376A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16859976 | |||||||
| chr19:16860226 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0192 |
3 | HG02976.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1059-2126C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860226 | |||||||
| chr19:16860300 | G | C | 1 | a0001c0002t0003g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1059-2052G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860300 | |||||||
| chr19:16860331 | G | T | 4 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0008g0122 others(1): Show |
4 | HG02258.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-2021G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860331 | |||||||
| chr19:16860339 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1059-2013C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860339 | |||||||
| chr19:16860366 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1059-1986C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860366 | |||||||
| chr19:16860408 | T | C | 9 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(6): Show |
9 | HG01074.hp2 HG01123.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059-1944T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860408 | |||||||
| chr19:16860596 | C | CT | 25 | a0001c0001t0001g0197 a0001c0001t0001g0206 a0001c0001t0001g0210 others(22): Show |
25 | HG00423.hp2 HG00733.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1059-1734dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16860596 | ||||||
| chr19:16860596 | C | CTT | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059-1735_1059-173 others(6): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16860596 | ||||||
| chr19:16860596 | CT | C | 8 | a0001c0001t0001g0217 a0001c0001t0002g0034 a0001c0001t0002g0139 others(5): Show |
8 | HG01070.hp1 HG01168.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059-1734delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16860596 | ||||||
| chr19:16860631 | C | T | 9 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059-1721C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860631 | |||||||
| chr19:16860663 | T | G | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1059-1689T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860663 | |||||||
| chr19:16860711 | C | T | 6 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0139 others(3): Show |
9 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059-1641C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860711 | |||||||
| chr19:16860727 | C | G | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059-1625C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860727 | |||||||
| chr19:16860845 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1059-1507G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860845 | |||||||
| chr19:16860885 | G | A | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1059-1467G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860885 | |||||||
| chr19:16860899 | G | A | 49 | a0001c0001t0007g0170 a0001c0001t0007g0182 a0001c0002t0003g0004 others(46): Show |
56 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1059-1453G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860899 | |||||||
| chr19:16860956 | C | G | 1 | a0001c0001t0002g0150 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1059-1396C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16860956 | |||||||
| chr19:16861293 | G | A | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059-1059G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16861293 | |||||||
| chr19:16861528 | C | T | 1 | a0001c0001t0002g0129 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1059-824C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16861528 | |||||||
| chr19:16861652 | A | G | 3 | a0001c0002t0003g0044 a0001c0002t0003g0045 a0001c0002t0003g0083 |
3 | NA18942.hp2 NA18963.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1059-700A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16861652 | |||||||
| chr19:16861762 | T | TC | 8 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059-589dupC | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16861762 | ||||||
| chr19:16861763 | C | CA | 33 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0101 others(30): Show |
35 | HG00609.hp2 HG00735.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1059-568dupA | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16861763 | ||||||
| chr19:16861763 | CA | C | 8 | a0001c0001t0001g0200 a0001c0001t0002g0136 a0001c0001t0002g0298 others(5): Show |
8 | HG01257.hp2 HG03704.hp1 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.1059-568delA | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr19 | 16861763 | ||||||
| chr19:16861930 | A | C | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059-422A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16861930 | |||||||
| chr19:16861986 | G | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1059-366G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 8/18 | chr19 | 16861986 | |||||||
| chr19:16862770 | A | C | 1 | a0001c0001t0001g0249 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1266+211A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 9/18 | chr19 | 16862770 | |||||||
| chr19:16863817 | G | A | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1383+21G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16863817 | |||||||
| chr19:16863825 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1383+29C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16863825 | |||||||
| chr19:16863945 | C | T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(27): Show |
32 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.1383+149C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16863945 | |||||||
| chr19:16864072 | T | C | 5 | a0001c0001t0001g0097 a0001c0001t0001g0099 a0001c0001t0001g0111 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1383+276T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16864072 | |||||||
| chr19:16864140 | A | AAAAATTA others(17): Show |
1 | a0001c0001t0004g0256 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1383+345_1383+368d others(26): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16864140 | ||||||
| chr19:16864158 | G | A | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1383+362G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16864158 | |||||||
| chr19:16864188 | A | G | 4 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0008g0122 others(1): Show |
4 | HG02258.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1383+392A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16864188 | |||||||
| chr19:16864227 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1383+431G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16864227 | |||||||
| chr19:16864305 | C | A | 123 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(120): Show |
136 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.1383+509C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16864305 | |||||||
| chr19:16864449 | C | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(42): Show |
47 | HG00609.hp2 HG00741.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.1383+653C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16864449 | |||||||
| chr19:16864491 | A | AGTT | 240 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(237): Show |
264 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1383+699_1383+701d others(5): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16864491 | ||||||
| chr19:16864837 | A | AT | 8 | a0001c0001t0001g0027 a0001c0001t0002g0120 a0001c0001t0002g0293 others(5): Show |
8 | HG01255.hp1 HG01978.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384-558dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16864837 | ||||||
| chr19:16864837 | AT | A | 6 | a0001c0001t0001g0217 a0001c0001t0012g0042 a0001c0002t0003g0055 others(3): Show |
6 | HG01256.hp2 HG01884.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-558delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16864837 | ||||||
| chr19:16864838 | T | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(115): Show |
130 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1384-572T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16864838 | |||||||
| chr19:16865059 | G | C | 46 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(43): Show |
48 | HG00609.hp2 HG00741.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.1384-351G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16865059 | |||||||
| chr19:16865209 | GT | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0192 |
3 | HG02976.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1384-198delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16865209 | ||||||
| chr19:16865264 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1384-146A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16865264 | |||||||
| chr19:16865304 | A | AC | 9 | a0001c0001t0005g0171 a0001c0001t0005g0172 a0001c0001t0005g0173 others(6): Show |
9 | HG00609.hp2 HG00735.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1384-105dupC | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16865304 | ||||||
| chr19:16865304 | A | ACC | 3 | a0001c0001t0005g0177 a0001c0001t0005g0180 a0001c0001t0005g0319 |
3 | HG01109.hp2 NA19009.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1384-105_1384-104i others(4): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16865304 | ||||||
| chr19:16865306 | A | AC | 114 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(111): Show |
124 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.1384-94dupC | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16865306 | ||||||
| chr19:16865306 | A | C | 46 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(43): Show |
48 | HG00609.hp2 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.1384-104A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16865306 | |||||||
| chr19:16865307 | C | T | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1384-103C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16865307 | |||||||
| chr19:16865316 | CA | C | 6 | a0001c0001t0001g0160 a0001c0001t0002g0117 a0001c0001t0002g0118 others(3): Show |
6 | HG01884.hp2 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1384-87delA | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr19 | 16865316 | ||||||
| chr19:16865317 | A | C | 9 | a0001c0001t0001g0159 a0001c0001t0001g0162 a0001c0001t0001g0183 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1384-93A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 10/18 | chr19 | 16865317 | |||||||
| chr19:16865694 | T | TCCCTC | 2 | a0001c0002t0003g0011 a0001c0002t0003g0068 |
3 | HG01516.hp1 HG02735.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1622+70_1622+74dup others(5): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr19 | 16865694 | ||||||
| chr19:16865697 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1622+49C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/18 | chr19 | 16865697 | |||||||
| chr19:16865713 | T | TA | 3 | a0001c0001t0001g0235 a0001c0001t0001g0257 a0001c0001t0001g0267 |
3 | HG02015.hp1 NA19010.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1622+65_1622+66ins others(1): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/18 | chr19 | 16865713 | |||||||
| chr19:16865781 | G | C | 1 | a0001c0001t0005g0266 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1622+133G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/18 | chr19 | 16865781 | |||||||
| chr19:16865798 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0001g0240 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1622+150C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/18 | chr19 | 16865798 | |||||||
| chr19:16865975 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1622+327G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/18 | chr19 | 16865975 | |||||||
| chr19:16866069 | A | G | 1 | a0001c0001t0002g0296 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1623-304A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/18 | chr19 | 16866069 | |||||||
| chr19:16866140 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1623-233T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/18 | chr19 | 16866140 | |||||||
| chr19:16866249 | G | C | 138 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(135): Show |
151 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1623-124G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 11/18 | chr19 | 16866249 | |||||||
| chr19:16866630 | T | A | 1 | a0001c0001t0004g0256 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1806+74T>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16866630 | |||||||
| chr19:16866647 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1806+91G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16866647 | |||||||
| chr19:16866665 | C | T | 2 | a0001c0001t0004g0221 a0001c0001t0004g0223 |
2 | NA18940.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1806+109C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16866665 | |||||||
| chr19:16866676 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1806+120C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16866676 | |||||||
| chr19:16866818 | G | A | 5 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(2): Show |
5 | HG02818.hp2 HG02895.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1806+262G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16866818 | |||||||
| chr19:16866886 | G | A | 183 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(180): Show |
198 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.1806+330G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16866886 | |||||||
| chr19:16867054 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1806+498C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867054 | |||||||
| chr19:16867082 | C | T | 1 | a0001c0001t0008g0122 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1806+526C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867082 | |||||||
| chr19:16867197 | G | A | 45 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(42): Show |
47 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1806+641G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867197 | |||||||
| chr19:16867257 | T | C | 1 | a0001c0001t0002g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1806+701T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867257 | |||||||
| chr19:16867341 | C | T | 1 | a0001c0001t0005g0172 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1806+785C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867341 | |||||||
| chr19:16867516 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1806+960C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867516 | |||||||
| chr19:16867568 | C | T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(27): Show |
32 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.1806+1012C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867568 | |||||||
| chr19:16867600 | C | T | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1806+1044C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867600 | |||||||
| chr19:16867686 | G | A | 135 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(132): Show |
148 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.1806+1130G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867686 | |||||||
| chr19:16867711 | G | A | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1806+1155G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867711 | |||||||
| chr19:16867739 | C | G | 15 | a0001c0001t0005g0123 a0001c0001t0005g0171 a0001c0001t0005g0172 others(12): Show |
15 | HG00609.hp2 HG00741.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1806+1183C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867739 | |||||||
| chr19:16867800 | G | T | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1806+1244G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867800 | |||||||
| chr19:16867817 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1806+1261C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867817 | |||||||
| chr19:16867859 | C | A | 47 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0011 others(44): Show |
54 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1806+1303C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867859 | |||||||
| chr19:16867981 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1806+1425G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867981 | |||||||
| chr19:16867990 | G | GTGTGGTC others(59): Show |
1 | a0001c0001t0001g0217 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1806+1434_1806+143 others(70): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867990 | |||||||
| chr19:16867991 | C | A | 1 | a0001c0001t0001g0217 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1806+1435C>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867991 | |||||||
| chr19:16867993 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1806+1437G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16867993 | |||||||
| chr19:16868188 | C | T | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1807-1272C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868188 | |||||||
| chr19:16868209 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1807-1251G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868209 | |||||||
| chr19:16868258 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1807-1202G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868258 | |||||||
| chr19:16868305 | C | G | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1807-1155C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868305 | |||||||
| chr19:16868310 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1807-1150G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868310 | |||||||
| chr19:16868328 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1807-1132C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868328 | |||||||
| chr19:16868347 | G | T | 1 | a0001c0001t0004g0256 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1807-1113G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868347 | |||||||
| chr19:16868348 | T | C | 1 | a0001c0001t0004g0256 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1807-1112T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868348 | |||||||
| chr19:16868357 | C | T | 4 | a0001c0001t0001g0217 a0001c0001t0001g0226 a0001c0001t0001g0247 others(1): Show |
4 | HG02132.hp2 NA18974.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.1807-1103C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868357 | |||||||
| chr19:16868377 | A | C | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-1083A>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868377 | |||||||
| chr19:16868455 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-1005G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868455 | |||||||
| chr19:16868456 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-1004A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868456 | |||||||
| chr19:16868457 | G | GCCCTGGT others(5): Show |
1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-1003_1807-100 others(16): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868457 | |||||||
| chr19:16868465 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-995G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868465 | |||||||
| chr19:16868477 | T | G | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-983T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868477 | |||||||
| chr19:16868484 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-976G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868484 | |||||||
| chr19:16868498 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-962G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868498 | |||||||
| chr19:16868500 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-960G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868500 | |||||||
| chr19:16868519 | G | C | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-941G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868519 | |||||||
| chr19:16868537 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-923A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868537 | |||||||
| chr19:16868578 | G | T | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1807-882G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868578 | |||||||
| chr19:16868688 | C | T | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1807-772C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868688 | |||||||
| chr19:16868782 | G | A | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1807-678G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16868782 | |||||||
| chr19:16868791 | GGCTGGTG others(3): Show |
G | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1807-657_1807-648d others(12): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr19 | 16868791 | ||||||
| chr19:16869054 | A | G | 55 | a0001c0002t0003g0004 a0001c0002t0003g0007 a0001c0002t0003g0011 others(52): Show |
64 | HG00408.hp1 HG00423.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.1807-406A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16869054 | |||||||
| chr19:16869207 | C | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0028 others(6): Show |
10 | HG02559.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1807-253C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16869207 | |||||||
| chr19:16869298 | A | G | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1807-162A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16869298 | |||||||
| chr19:16869329 | C | T | 4 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0008g0122 others(1): Show |
4 | HG02258.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1807-131C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16869329 | |||||||
| chr19:16869384 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1807-76C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16869384 | |||||||
| chr19:16869433 | A | G | 9 | a0001c0001t0001g0100 a0001c0001t0001g0159 a0001c0001t0001g0160 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1807-27A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 12/18 | chr19 | 16869433 | |||||||
| chr19:16870096 | G | C | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2422+21G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870096 | |||||||
| chr19:16870097 | G | A | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2422+22G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870097 | |||||||
| chr19:16870105 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG01169.hp2 HG02970.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2422+30C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870105 | |||||||
| chr19:16870233 | A | G | 45 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(42): Show |
47 | HG00609.hp2 HG00741.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.2422+158A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870233 | |||||||
| chr19:16870245 | TCTCACGT others(19): Show |
T | 1 | a0001c0001t0001g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2422+173_2422+198d others(28): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16870245 | ||||||
| chr19:16870250 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2422+175C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870250 | |||||||
| chr19:16870273 | T | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0206 a0001c0001t0001g0274 |
3 | HG01358.hp2 HG01981.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2422+198T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870273 | |||||||
| chr19:16870374 | A | G | 186 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(183): Show |
201 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.2422+299A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870374 | |||||||
| chr19:16870387 | C | CT | 12 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(9): Show |
12 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.2422+327dupT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16870387 | ||||||
| chr19:16870387 | CT | C | 125 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(122): Show |
138 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.2422+327delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16870387 | ||||||
| chr19:16870445 | C | T | 1 | a0001c0001t0014g0043 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2422+370C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870445 | |||||||
| chr19:16870544 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2422+469C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870544 | |||||||
| chr19:16870551 | A | G | 2 | a0001c0001t0002g0165 a0001c0001t0012g0042 |
2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2422+476A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870551 | |||||||
| chr19:16870711 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2423-518C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870711 | |||||||
| chr19:16870712 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2423-517G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870712 | |||||||
| chr19:16870716 | AT | A | 232 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(229): Show |
254 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.2423-503delT | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16870716 | ||||||
| chr19:16870806 | G | A | 2 | a0001c0001t0006g0093 a0001c0001t0006g0094 |
2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2423-423G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870806 | |||||||
| chr19:16870901 | A | G | 3 | a0001c0001t0001g0191 a0001c0001t0001g0246 a0001c0001t0002g0166 |
3 | HG00438.hp1 HG02056.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.2423-328A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870901 | |||||||
| chr19:16870907 | T | C | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2423-322T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16870907 | |||||||
| chr19:16870964 | TACAGGCA others(6): Show |
T | 4 | a0001c0001t0004g0021 a0001c0001t0004g0216 a0001c0001t0004g0254 others(1): Show |
5 | NA18946.hp2 NA18950.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2423-262_2423-250d others(15): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr19 | 16870964 | ||||||
| chr19:16871024 | C | T | 2 | a0001c0001t0002g0144 a0001c0001t0002g0145 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2423-205C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16871024 | |||||||
| chr19:16871176 | C | T | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2423-53C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 13/18 | chr19 | 16871176 | |||||||
| chr19:16871466 | C | T | 11 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.2592+68C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16871466 | |||||||
| chr19:16871533 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0008g0122 a0001c0001t0008g0163 |
3 | HG02258.hp1 HG03098.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2592+135C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16871533 | |||||||
| chr19:16871534 | G | A | 3 | a0001c0002t0003g0059 a0001c0002t0003g0062 a0001c0002t0003g0063 |
3 | NA18945.hp2 NA18959.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2592+136G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16871534 | |||||||
| chr19:16871540 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2592+142C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16871540 | |||||||
| chr19:16871581 | T | C | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2592+183T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16871581 | |||||||
| chr19:16871652 | A | G | 1 | a0001c0001t0001g0203 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2592+254A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16871652 | |||||||
| chr19:16871685 | C | G | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2592+287C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16871685 | |||||||
| chr19:16871729 | G | C | 1 | a0001c0001t0004g0227 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2592+331G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16871729 | |||||||
| chr19:16871837 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2592+439A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16871837 | |||||||
| chr19:16871859 | C | T | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2592+461C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16871859 | |||||||
| chr19:16872018 | G | A | 1 | a0001c0001t0005g0181 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2592+620G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872018 | |||||||
| chr19:16872019 | G | C | 183 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(180): Show |
198 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.2592+621G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872019 | |||||||
| chr19:16872098 | C | T | 2 | a0001c0001t0007g0170 a0001c0001t0007g0182 |
2 | HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2592+700C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872098 | |||||||
| chr19:16872330 | A | G | 30 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(27): Show |
32 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.2592+932A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872330 | |||||||
| chr19:16872396 | C | T | 1 | a0004c0017t0001g0208 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2592+998C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872396 | |||||||
| chr19:16872442 | T | G | 7 | a0001c0001t0001g0195 a0001c0001t0001g0228 a0001c0001t0001g0242 others(4): Show |
7 | HG00323.hp2 HG01099.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.2592+1044T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872442 | |||||||
| chr19:16872590 | C | T | 42 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0008 others(39): Show |
55 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.2592+1192C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872590 | |||||||
| chr19:16872603 | C | T | 2 | a0001c0001t0001g0160 a0002c0005t0001g0161 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2592+1205C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872603 | |||||||
| chr19:16872686 | C | T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(27): Show |
32 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.2592+1288C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872686 | |||||||
| chr19:16872739 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2592+1341G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872739 | |||||||
| chr19:16872812 | G | C | 7 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0236 others(4): Show |
7 | HG01109.hp1 HG02451.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2592+1414G>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16872812 | |||||||
| chr19:16873055 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2592+1657T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16873055 | |||||||
| chr19:16873189 | G | A | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2592+1791G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16873189 | |||||||
| chr19:16873245 | G | A | 8 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2592+1847G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16873245 | |||||||
| chr19:16873448 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2592+2050A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16873448 | |||||||
| chr19:16873469 | A | G | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2592+2071A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16873469 | |||||||
| chr19:16873488 | G | A | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2592+2090G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16873488 | |||||||
| chr19:16873500 | A | G | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2592+2102A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16873500 | |||||||
| chr19:16873522 | T | TC | 23 | a0001c0001t0001g0239 a0001c0001t0002g0119 a0001c0001t0002g0133 others(20): Show |
23 | HG00438.hp2 HG01109.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.2592+2136dupC | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16873522 | ||||||
| chr19:16873522 | TC | T | 135 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0020 others(132): Show |
148 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.2592+2136delC | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16873522 | ||||||
| chr19:16873817 | C | G | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2593-2238C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16873817 | |||||||
| chr19:16873863 | C | T | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2593-2192C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16873863 | |||||||
| chr19:16874222 | A | T | 44 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(41): Show |
46 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.2593-1833A>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16874222 | |||||||
| chr19:16874257 | C | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2593-1798C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16874257 | |||||||
| chr19:16874296 | AGGTCTGG others(3): Show |
A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0312 |
2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2593-1753_2593-174 others(14): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16874296 | ||||||
| chr19:16874324 | G | T | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2593-1731G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16874324 | |||||||
| chr19:16874386 | GTTTGGTC others(50): Show |
G | 2 | a0001c0001t0006g0093 a0001c0001t0006g0094 |
2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.2593-1652_2593-159 others(61): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16874386 | ||||||
| chr19:16874497 | TTGATTTG others(3): Show |
T | 1 | a0001c0001t0001g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2593-1545_2593-153 others(14): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16874497 | ||||||
| chr19:16874634 | T | C | 104 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0022 others(101): Show |
113 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.2593-1421T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16874634 | |||||||
| chr19:16874647 | G | A | 30 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(27): Show |
32 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.2593-1408G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16874647 | |||||||
| chr19:16874742 | A | G | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2593-1313A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16874742 | |||||||
| chr19:16874816 | T | G | 119 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(116): Show |
131 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.2593-1239T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16874816 | |||||||
| chr19:16875095 | T | C | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2593-960T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16875095 | |||||||
| chr19:16875158 | GGGTCT | G | 3 | a0001c0001t0002g0039 a0001c0001t0002g0041 a0001c0012t0002g0040 |
3 | HG01346.hp2 HG01515.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.2593-880_2593-876d others(7): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875158 | ||||||
| chr19:16875158 | GGGTCTGG others(22): Show |
G | 1 | a0001c0001t0001g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2593-874_2593-846d others(31): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875158 | ||||||
| chr19:16875158 | GGGTCTGG others(56): Show |
G | 3 | a0001c0001t0002g0290 a0001c0001t0002g0291 a0001c0001t0002g0296 |
3 | HG00558.hp1 HG02027.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.2593-854_2593-792d others(65): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875158 | ||||||
| chr19:16875181 | T | TTGGTC | 3 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0002c0005t0001g0161 |
3 | HG01884.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2593-851_2593-847d others(7): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875181 | ||||||
| chr19:16875191 | CTGGTCTG others(22): Show |
C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0212 a0010c0009t0001g0193 |
3 | NA18966.hp1 NA18998.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.2593-846_2593-818d others(31): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875191 | ||||||
| chr19:16875286 | CTGGTCTG others(4): Show |
C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2593-757_2593-747d others(13): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875286 | ||||||
| chr19:16875378 | CTGGTCTG others(7): Show |
C | 4 | a0001c0004t0002g0124 a0001c0004t0002g0135 a0001c0004t0002g0142 others(1): Show |
4 | HG02109.hp1 HG02145.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2593-664_2593-651d others(16): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875378 | ||||||
| chr19:16875474 | TTGGTCTG others(9): Show |
T | 1 | a0001c0001t0017g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2593-567_2593-552d others(18): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875474 | ||||||
| chr19:16875524 | CTGGTCTG others(7): Show |
C | 2 | a0001c0001t0002g0295 a0001c0014t0001g0095 |
2 | HG01884.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.2593-504_2593-491d others(16): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875524 | ||||||
| chr19:16875552 | T | TTGGTC | 4 | a0001c0002t0003g0058 a0001c0002t0003g0059 a0001c0002t0003g0062 others(1): Show |
4 | HG00733.hp1 NA18945.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.2593-478_2593-474d others(7): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875552 | ||||||
| chr19:16875552 | TTGGTC | T | 9 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(6): Show |
9 | HG01884.hp2 HG02258.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2593-478_2593-474d others(7): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875552 | ||||||
| chr19:16875552 | TTGGTCTG others(3): Show |
T | 1 | a0001c0001t0002g0119 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2593-483_2593-474d others(12): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875552 | ||||||
| chr19:16875625 | C | CTGGTCTG others(36): Show |
1 | a0001c0001t0005g0178 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2593-412_2593-370d others(45): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875625 | ||||||
| chr19:16875643 | T | G | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2593-412T>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16875643 | |||||||
| chr19:16875644 | TTGGTC | T | 8 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2593-393_2593-389d others(7): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875644 | ||||||
| chr19:16875645 | T | C | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2593-410T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16875645 | |||||||
| chr19:16875646 | G | T | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2593-409G>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16875646 | |||||||
| chr19:16875649 | C | T | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2593-406C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16875649 | |||||||
| chr19:16875668 | TTGGTCTG others(3): Show |
T | 1 | a0001c0003t0002g0050 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2593-366_2593-357d others(12): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875668 | ||||||
| chr19:16875699 | G | A | 2 | a0001c0001t0004g0229 a0001c0001t0004g0262 |
2 | HG00280.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.2593-356G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16875699 | |||||||
| chr19:16875760 | TTGGTCTG others(27): Show |
T | 1 | a0001c0001t0005g0123 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2593-263_2593-230d others(36): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875760 | ||||||
| chr19:16875774 | TTGGTC | T | 6 | a0001c0001t0001g0261 a0001c0001t0002g0129 a0001c0001t0004g0222 others(3): Show |
7 | HG01243.hp1 NA18986.hp1 NA19055.hp1 others(4): Show |
intron_variant | MODIFIER | c.2593-253_2593-249d others(7): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875774 | ||||||
| chr19:16875856 | TTGGTC | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0001g0312 others(3): Show |
9 | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2593-171_2593-167d others(7): Show |
SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr19 | 16875856 | ||||||
| chr19:16875914 | T | C | 7 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0162 others(4): Show |
7 | HG01884.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2593-141T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16875914 | |||||||
| chr19:16875943 | C | T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(27): Show |
32 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.2593-112C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16875943 | |||||||
| chr19:16875949 | C | G | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2593-106C>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 14/18 | chr19 | 16875949 | |||||||
| chr19:16876257 | G | A | 2 | a0001c0002t0003g0089 a0001c0002t0003g0091 |
2 | NA18965.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2766+29G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 15/18 | chr19 | 16876257 | |||||||
| chr19:16876282 | G | A | 30 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0027 others(27): Show |
32 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.2766+54G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 15/18 | chr19 | 16876282 | |||||||
| chr19:16876330 | G | A | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2766+102G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 15/18 | chr19 | 16876330 | |||||||
| chr19:16876451 | C | T | 4 | a0001c0001t0004g0021 a0001c0001t0004g0216 a0001c0001t0004g0254 others(1): Show |
5 | NA18946.hp2 NA18950.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2767-35C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 15/18 | chr19 | 16876451 | |||||||
| chr19:16876620 | C | T | 4 | a0001c0001t0001g0162 a0001c0001t0001g0183 a0001c0001t0008g0122 others(1): Show |
4 | HG02258.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2859+42C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 16/18 | chr19 | 16876620 | |||||||
| chr19:16876667 | C | T | 13 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0001g0204 others(10): Show |
13 | HG01109.hp1 HG01496.hp2 HG01975.hp2 others(10): Show |
intron_variant | MODIFIER | c.2859+89C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 16/18 | chr19 | 16876667 | |||||||
| chr19:16876747 | C | T | 1 | a0001c0001t0012g0042 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2859+169C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 16/18 | chr19 | 16876747 | |||||||
| chr19:16876880 | G | A | 1 | a0001c0001t0016g0321 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2859+302G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 16/18 | chr19 | 16876880 | |||||||
| chr19:16877007 | G | A | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2859+429G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 16/18 | chr19 | 16877007 | |||||||
| chr19:16877241 | C | T | 1 | a0001c0014t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2860-304C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 16/18 | chr19 | 16877241 | |||||||
| chr19:16877390 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2860-155C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 16/18 | chr19 | 16877390 | |||||||
| chr19:16877416 | C | T | 1 | a0001c0001t0014g0043 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2860-129C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 16/18 | chr19 | 16877416 | |||||||
| chr19:16877645 | A | G | 199 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(196): Show |
221 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(218): Show |
splice_region_variant&intron_variant | LOW | c.2954+6A>G | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 17/18 | chr19 | 16877645 | |||||||
| chr19:16877665 | T | C | 241 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(238): Show |
265 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.2954+26T>C | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 17/18 | chr19 | 16877665 | |||||||
| chr19:16877674 | C | T | 1 | a0008c0019t0001g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2954+35C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 17/18 | chr19 | 16877674 | |||||||
| chr19:16877794 | G | A | 1 | a0001c0002t0003g0075 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2954+155G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 17/18 | chr19 | 16877794 | |||||||
| chr19:16877939 | G | A | 4 | a0001c0001t0002g0117 a0001c0001t0002g0118 a0001c0001t0002g0119 others(1): Show |
4 | HG02818.hp2 HG02895.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2955-244G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 17/18 | chr19 | 16877939 | |||||||
| chr19:16877975 | G | A | 121 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(118): Show |
134 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.2955-208G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 17/18 | chr19 | 16877975 | |||||||
| chr19:16877996 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2955-187G>A | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 17/18 | chr19 | 16877996 | |||||||
| chr19:16878050 | C | T | 1 | a0001c0002t0003g0092 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2955-133C>T | SIN3B | ENSG00000127511.10 | transcript | ENST00000248054.10 | protein_coding | 17/18 | chr19 | 16878050 |