Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9798 |
| ensemblid | ENSG00000182149.21 |
| hgncid | 28977 |
| symbol | IST1 |
| name | IST1 factor associated with ESCRT-III |
| refseq_nuc | NM_001270975.2 |
| refseq_prot | NP_001257904.1 |
| ensembl_nuc | ENST00000378799.11 |
| ensembl_prot | ENSP00000368076.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 71895531 |
| end | 71931199 |
| strand | + |
| ver | v1.2 |
| region | chr16:71895531-71931199 |
| region5000 | chr16:71890531-71936199 |
| regionname0 | IST1_chr16_71895531_71931199 |
| regionname5000 | IST1_chr16_71890531_71936199 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 366 | 218 | 58 | 53 | 77 | 11 | 18 | 61 | IST1_chr16_71890531_71936199 | IST1 | MLGSG others(361): Show |
chr16 | 71890531 | 71936199 |
| a0002 | 0/1 | 364 | 119 | 18 | 19 | 55 | 5 | 21 | 47 | IST1_chr16_71890531_71936199 | IST1 | MLGSG others(359): Show |
chr16 | 71890531 | 71936199 |
| a0003 | 0/0 | 368 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | MLGSG others(363): Show |
chr16 | 71890531 | 71936199 |
| a0004 | 0/0 | 364 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | MLGSG others(359): Show |
chr16 | 71890531 | 71936199 |
| a0005 | 0/0 | 366 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | MLGSG others(361): Show |
chr16 | 71890531 | 71936199 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1098 | 215 | 57 | 51 | 77 | 11 | 18 | IST1_chr16_71890531_71936199 | IST1 | ATGCT others(1093): Show |
chr16 | 71890531 | 71936199 | ||
| a0001c0007 | 0/0 | 1098 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATGCT others(1093): Show |
chr16 | 71890531 | 71936199 | ||
| a0001c0009 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATGCT others(1093): Show |
chr16 | 71890531 | 71936199 | ||
| a0001c0010 | 0/0 | 1098 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATGCT others(1093): Show |
chr16 | 71890531 | 71936199 | ||
| a0002c0002 | 0/0 | 1092 | 80 | 4 | 6 | 52 | 2 | 16 | IST1_chr16_71890531_71936199 | IST1 | ATGCT others(1087): Show |
chr16 | 71890531 | 71936199 | ||
| a0002c0003 | 0/1 | 1092 | 34 | 14 | 10 | 3 | 1 | 5 | IST1_chr16_71890531_71936199 | IST1 | ATGCT others(1087): Show |
chr16 | 71890531 | 71936199 | ||
| a0002c0005 | 0/0 | 1092 | 5 | 0 | 3 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATGCT others(1087): Show |
chr16 | 71890531 | 71936199 | ||
| a0003c0004 | 0/0 | 1104 | 12 | 12 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATGCT others(1099): Show |
chr16 | 71890531 | 71936199 | ||
| a0004c0006 | 0/0 | 1092 | 2 | 0 | 0 | 0 | 0 | 2 | IST1_chr16_71890531_71936199 | IST1 | ATGCT others(1087): Show |
chr16 | 71890531 | 71936199 | ||
| a0005c0008 | 0/0 | 1098 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | ATGCT others(1093): Show |
chr16 | 71890531 | 71936199 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4561 | 114 | 18 | 24 | 58 | 5 | 8 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0003 | 0/0 | 4561 | 31 | 29 | 2 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0004 | 0/0 | 4561 | 21 | 0 | 13 | 3 | 1 | 4 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0005 | 0/0 | 4561 | 18 | 1 | 6 | 5 | 2 | 4 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0007 | 0/0 | 4561 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0008 | 0/0 | 4561 | 8 | 0 | 0 | 7 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0009 | 0/0 | 4561 | 4 | 0 | 4 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0010 | 0/0 | 4561 | 2 | 0 | 0 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0011 | 0/0 | 4561 | 3 | 2 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0012 | 0/0 | 4561 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0013 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0014 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0015 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0019 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0022 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0023 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0024 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0025 | 0/0 | 4561 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0026 | 0/0 | 4561 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0001t0030 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0007t0001 | 0/0 | 4561 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0009t0005 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0001c0010t0001 | 0/0 | 4561 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| a0002c0002t0002 | 0/0 | 4549 | 76 | 4 | 6 | 49 | 2 | 15 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4544): Show |
chr16 | 71890531 | 71936199 |
| a0002c0002t0016 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4544): Show |
chr16 | 71890531 | 71936199 |
| a0002c0002t0017 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4544): Show |
chr16 | 71890531 | 71936199 |
| a0002c0002t0018 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4544): Show |
chr16 | 71890531 | 71936199 |
| a0002c0002t0031 | 0/0 | 4549 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4544): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0001 | 0/0 | 4555 | 12 | 5 | 4 | 0 | 0 | 3 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0002 | 0/0 | 4549 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4544): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0003 | 0/0 | 4555 | 7 | 7 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0004 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0005 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0007 | 0/1 | 4555 | 7 | 0 | 4 | 0 | 1 | 1 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0008 | 0/0 | 4555 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0010 | 0/0 | 4555 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0020 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0028 | 0/0 | 4555 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0002c0003t0029 | 0/0 | 4555 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0002c0005t0002 | 0/0 | 4549 | 5 | 0 | 3 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4544): Show |
chr16 | 71890531 | 71936199 |
| a0003c0004t0006 | 0/0 | 4559 | 11 | 11 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4554): Show |
chr16 | 71890531 | 71936199 |
| a0003c0004t0027 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4554): Show |
chr16 | 71890531 | 71936199 |
| a0004c0006t0007 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0004c0006t0021 | 0/0 | 4555 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4550): Show |
chr16 | 71890531 | 71936199 |
| a0005c0008t0001 | 0/0 | 4561 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | ATTTT others(4556): Show |
chr16 | 71890531 | 71936199 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 10 | 1 | 3 | 6 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0005 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0007g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0008g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0008g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0008g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0008g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0009g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0009g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0009g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0009g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0010g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0011g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0012g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0012g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0013g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0014g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0015g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0019g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0022g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0023g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0024g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0025g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0026g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0001t0030g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0007t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0009t0005g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0001c0010t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0001 | 0/0 | 10 | 0 | 2 | 6 | 0 | 2 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0016g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0017g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0018g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0002t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0007g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0007g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0007g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0007g0083 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0007g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0008g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0010g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0020g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0028g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0003t0029g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0005t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0005t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0005t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0002c0005t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0003c0004t0006g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0003c0004t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0003c0004t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0003c0004t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0003c0004t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0003c0004t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0003c0004t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0003c0004t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0003c0004t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0003c0004t0027g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0004c0006t0007g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0004c0006t0021g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| a0005c0008t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0053 | EUR | GBR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0019 | EUR | GBR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00323 | hp1 | a0002 | c0005 | t0002 | g0017 | EUR | FIN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0108 | EUR | FIN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00609 | hp1 | a0001 | c0001 | t0024 | g0151 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00609 | hp2 | a0001 | c0001 | t0008 | g0255 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0249 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00733 | hp1 | a0002 | c0003 | t0029 | g0082 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0060 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00741 | hp1 | a0001 | c0001 | t0014 | g0047 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01069 | hp2 | a0002 | c0005 | t0002 | g0113 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0050 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01071 | hp2 | a0002 | c0005 | t0002 | g0017 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01074 | hp1 | a0002 | c0003 | t0007 | g0008 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01074 | hp2 | a0002 | c0003 | t0007 | g0081 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0135 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0287 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0167 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0158 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0126 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0154 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01175 | hp1 | a0002 | c0003 | t0007 | g0084 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0257 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01243 | hp1 | a0002 | c0003 | t0001 | g0231 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0148 | AMR | PUR | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01256 | hp2 | a0001 | c0009 | t0005 | g0180 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0156 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01346 | hp1 | a0002 | c0005 | t0002 | g0102 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01346 | hp2 | a0001 | c0010 | t0001 | g0216 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01358 | hp1 | a0002 | c0003 | t0010 | g0020 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0059 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01361 | hp2 | a0002 | c0003 | t0007 | g0177 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01433 | hp2 | a0001 | c0001 | t0030 | g0013 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01515 | hp1 | a0001 | c0001 | t0011 | g0073 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0157 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01516 | hp2 | a0001 | c0001 | t0005 | g0162 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01517 | hp2 | a0001 | c0001 | t0010 | g0020 | EUR | IBS | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01884 | hp1 | a0002 | c0003 | t0003 | g0016 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01891 | hp1 | a0003 | c0004 | t0006 | g0077 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01891 | hp2 | a0001 | c0001 | t0023 | g0165 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0021 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01981 | hp2 | a0001 | c0001 | t0009 | g0052 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01993 | hp1 | a0001 | c0001 | t0009 | g0005 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0253 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02027 | hp1 | a0001 | c0001 | t0019 | g0198 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0058 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02132 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02145 | hp2 | a0002 | c0003 | t0003 | g0100 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0131 | EAS | CDX | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0045 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0159 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02258 | hp2 | a0003 | c0004 | t0006 | g0067 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02280 | hp1 | a0002 | c0003 | t0003 | g0016 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02280 | hp2 | a0002 | c0003 | t0001 | g0189 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0051 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02300 | hp1 | a0001 | c0001 | t0009 | g0038 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | PEL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02451 | hp1 | a0002 | c0003 | t0003 | g0096 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02451 | hp2 | a0002 | c0003 | t0028 | g0031 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02602 | hp1 | a0002 | c0003 | t0002 | g0145 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02602 | hp2 | a0002 | c0003 | t0007 | g0008 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02630 | hp2 | a0002 | c0003 | t0001 | g0213 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02683 | hp2 | a0004 | c0006 | t0021 | g0079 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0123 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0227 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02717 | hp2 | a0002 | c0003 | t0003 | g0097 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0116 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0171 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0260 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02809 | hp1 | a0002 | c0003 | t0003 | g0094 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0119 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0075 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0074 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0085 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02896 | hp2 | a0003 | c0004 | t0006 | g0072 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0066 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02922 | hp1 | a0001 | c0007 | t0001 | g0054 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02965 | hp2 | a0003 | c0004 | t0006 | g0007 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02970 | hp2 | a0003 | c0004 | t0006 | g0070 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0124 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0285 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03130 | hp1 | a0003 | c0004 | t0027 | g0078 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03139 | hp1 | a0002 | c0003 | t0003 | g0098 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0284 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0184 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03225 | hp1 | a0002 | c0003 | t0020 | g0064 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0183 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03239 | hp1 | a0004 | c0006 | t0007 | g0008 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0048 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0178 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03491 | hp2 | a0002 | c0002 | t0002 | g0182 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0181 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0019 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0274 | AFR | ESN | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0215 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03540 | hp2 | a0003 | c0004 | t0006 | g0071 | AFR | GWD | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0035 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0117 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0120 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0127 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03704 | hp2 | a0001 | c0001 | t0005 | g0021 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03831 | hp2 | a0005 | c0008 | t0001 | g0240 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0118 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0202 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0275 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0169 | SAS | BEB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0121 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG04199 | hp2 | a0002 | c0002 | t0018 | g0105 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG04204 | hp1 | a0001 | c0001 | t0025 | g0153 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0130 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG04228 | hp1 | a0001 | c0001 | t0005 | g0160 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | STU | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | YRI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18906 | hp2 | a0003 | c0004 | t0006 | g0007 | AFR | YRI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18951 | hp1 | a0001 | c0001 | t0008 | g0211 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18953 | hp2 | a0001 | c0001 | t0026 | g0155 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18957 | hp2 | a0002 | c0002 | t0016 | g0018 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0163 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18965 | hp2 | a0001 | c0001 | t0013 | g0208 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18966 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18968 | hp1 | a0001 | c0001 | t0005 | g0149 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18968 | hp2 | a0002 | c0003 | t0008 | g0222 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18971 | hp2 | a0002 | c0003 | t0005 | g0152 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18975 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18979 | hp2 | a0002 | c0002 | t0031 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18987 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18988 | hp1 | a0001 | c0001 | t0008 | g0273 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18990 | hp1 | a0002 | c0003 | t0004 | g0055 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19011 | hp1 | a0002 | c0002 | t0017 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0076 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19043 | hp1 | a0003 | c0004 | t0006 | g0007 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0164 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0170 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19089 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19091 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19240 | hp1 | a0003 | c0004 | t0006 | g0069 | AFR | YRI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | ASW | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ASW | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA20752 | hp1 | a0002 | c0003 | t0007 | g0080 | EUR | TSI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0107 | EUR | TSI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA20805 | hp1 | a0002 | c0005 | t0002 | g0103 | EUR | TSI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0061 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0110 | AMR | CLM | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02109 | hp2 | a0003 | c0004 | t0006 | g0068 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02486 | hp1 | a0001 | c0001 | t0015 | g0185 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0288 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | ACB | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | MSL | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG06807 | hp1 | a0001 | c0001 | t0022 | g0147 | AFR | USA | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| HG06807 | hp2 | a0003 | c0004 | t0006 | g0065 | AFR | USA | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | USA | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0128 | AFR | LWK | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0007 | g0083 | REF | REF | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0034 | REF | REF | IST1_chr16_71890531_71936199 | IST1 | chr16 | 71890531 | 71936199 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71921367 | G | A | 1 | a0004 | 2 | HG02683.hp2 HG03239.hp1 |
missense_variant | MODERATE | c.466G>A | p.Ala156Thr | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/10 | 540/4561 | 466/1101 | 156/366 | chr16 | 71921367 | |||
| chr16:71922608 | A | AATGCCC | 1 | a0003 | 12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
disruptive_inframe_insertion | MODERATE | c.705_710dupCATGCC | p.Pro237_Met238insMe others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/10 | 785/4561 | 711/1101 | 237/366 | INFO_REALIGN_3_PRIME | chr16 | 71922608 | ||
| chr16:71922608 | AATGCCC | A | 2 | a0002 a0004 |
120 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(117): Show |
disruptive_inframe_deletion | MODERATE | c.705_710delCATGCC | p.Met236_Pro237del | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/10 | 779/4561 | 705/1101 | 235/366 | INFO_REALIGN_3_PRIME | chr16 | 71922608 | ||
| chr16:71927632 | A | C | 1 | a0005 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.920A>C | p.Glu307Ala | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 994/4561 | 920/1101 | 307/366 | chr16 | 71927632 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71916547 | C | T | 3 | a0001c0010 a0002c0002 a0002c0005 |
86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
synonymous_variant | LOW | c.174C>T | p.His58His | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 3/10 | 248/4561 | 174/1101 | 58/366 | chr16 | 71916547 | |||
| chr16:71921411 | A | G | 1 | a0001c0009 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.510A>G | p.Ala170Ala | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/10 | 584/4561 | 510/1101 | 170/366 | chr16 | 71921411 | |||
| chr16:71922602 | G | A | 1 | a0002c0005 | 5 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
synonymous_variant | LOW | c.681G>A | p.Thr227Thr | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/10 | 755/4561 | 681/1101 | 227/366 | chr16 | 71922602 | |||
| chr16:71922662 | T | C | 1 | a0001c0007 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.741T>C | p.Tyr247Tyr | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/10 | 815/4561 | 741/1101 | 247/366 | chr16 | 71922662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71895555 | C | T | 2 | a0001c0001t0030 a0002c0002t0031 |
2 | HG01433.hp2 NA18979.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-50C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/10 | chr16 | 71895555 | |||||||
| chr16:71895574 | G | A | 3 | a0001c0001t0008 a0001c0001t0013 a0002c0003t0008 |
10 | HG00609.hp2 HG02083.hp1 HG02132.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-31G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/10 | 20067 | chr16 | 71895574 | ||||||
| chr16:71895585 | G | A | 1 | a0001c0001t0014 | 1 | HG00741.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/10 | 20056 | chr16 | 71895585 | ||||||
| chr16:71927862 | A | T | 2 | a0001c0001t0011 a0001c0001t0012 |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*49A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 49 | chr16 | 71927862 | ||||||
| chr16:71928003 | A | G | 21 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0010 others(18): Show |
58 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*190A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 190 | chr16 | 71928003 | ||||||
| chr16:71928053 | T | C | 1 | a0001c0001t0015 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*240T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 240 | chr16 | 71928053 | ||||||
| chr16:71928368 | A | G | 1 | a0002c0003t0029 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*555A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 555 | chr16 | 71928368 | ||||||
| chr16:71928416 | G | A | 1 | a0002c0002t0016 | 1 | NA18957.hp2 | 3_prime_UTR_variant | MODIFIER | c.*603G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 603 | chr16 | 71928416 | ||||||
| chr16:71928522 | G | A | 1 | a0002c0003t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*709G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 709 | chr16 | 71928522 | ||||||
| chr16:71928688 | G | C | 6 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0014 others(3): Show |
29 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*875G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 875 | chr16 | 71928688 | ||||||
| chr16:71928823 | A | G | 1 | a0002c0003t0028 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1010A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1010 | chr16 | 71928823 | ||||||
| chr16:71928966 | C | T | 1 | a0001c0001t0015 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1153C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1153 | chr16 | 71928966 | ||||||
| chr16:71928967 | TGTAGCTC others(1): Show |
T | 2 | a0003c0004t0006 a0003c0004t0027 |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1161_*1168delCAGT others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1161 | INFO_REALIGN_3_PRIME | chr16 | 71928967 | |||||
| chr16:71929000 | C | T | 1 | a0001c0001t0026 | 1 | NA18953.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1187C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1187 | chr16 | 71929000 | ||||||
| chr16:71929173 | G | C | 3 | a0001c0001t0022 a0001c0001t0023 a0002c0003t0028 |
3 | HG01891.hp2 HG02451.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1360G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1360 | chr16 | 71929173 | ||||||
| chr16:71929283 | C | T | 15 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0010 others(12): Show |
39 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1470C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1470 | chr16 | 71929283 | ||||||
| chr16:71929563 | G | A | 1 | a0001c0001t0013 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1750G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1750 | chr16 | 71929563 | ||||||
| chr16:71929579 | C | T | 2 | a0001c0001t0023 a0002c0003t0028 |
2 | HG01891.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1766C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1766 | chr16 | 71929579 | ||||||
| chr16:71929584 | G | A | 2 | a0003c0004t0006 a0003c0004t0027 |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1771G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1771 | chr16 | 71929584 | ||||||
| chr16:71929620 | C | A | 1 | a0002c0003t0020 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1807C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1807 | chr16 | 71929620 | ||||||
| chr16:71929788 | A | G | 1 | a0001c0001t0009 | 4 | HG01981.hp2 HG01993.hp1 HG02293.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1975A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 1975 | chr16 | 71929788 | ||||||
| chr16:71930018 | T | C | 1 | a0002c0002t0017 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2205T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2205 | chr16 | 71930018 | ||||||
| chr16:71930021 | C | T | 15 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0010 others(12): Show |
39 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2208C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2208 | chr16 | 71930021 | ||||||
| chr16:71930025 | A | G | 2 | a0001c0001t0003 a0002c0003t0003 |
38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2212A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2212 | chr16 | 71930025 | ||||||
| chr16:71930188 | G | A | 1 | a0001c0001t0025 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2375 | chr16 | 71930188 | ||||||
| chr16:71930272 | T | C | 2 | a0001c0001t0003 a0002c0003t0003 |
38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2459T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2459 | chr16 | 71930272 | ||||||
| chr16:71930399 | C | T | 7 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0025 others(4): Show |
25 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2586C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2586 | chr16 | 71930399 | ||||||
| chr16:71930409 | A | C | 1 | a0001c0001t0019 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2596A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2596 | chr16 | 71930409 | ||||||
| chr16:71930412 | A | G | 1 | a0001c0001t0012 | 2 | HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2599A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2599 | chr16 | 71930412 | ||||||
| chr16:71930458 | CAT | C | 7 | a0002c0002t0002 a0002c0002t0016 a0002c0002t0017 others(4): Show |
86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2646_*2647delAT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2646 | chr16 | 71930458 | ||||||
| chr16:71930535 | A | T | 1 | a0002c0002t0018 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2722A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2722 | chr16 | 71930535 | ||||||
| chr16:71930725 | A | G | 1 | a0003c0004t0027 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2912A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 2912 | chr16 | 71930725 | ||||||
| chr16:71930902 | C | T | 18 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0011 others(15): Show |
54 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3089C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 3089 | chr16 | 71930902 | ||||||
| chr16:71930969 | G | T | 1 | a0001c0001t0022 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3156G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 3156 | chr16 | 71930969 | ||||||
| chr16:71931072 | GTTTA | G | 7 | a0002c0002t0002 a0002c0002t0016 a0002c0002t0017 others(4): Show |
86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3263_*3266delATTT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 10/10 | 3263 | INFO_REALIGN_3_PRIME | chr16 | 71931072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:71895675 | G | C | 1 | a0002c0003t0028g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+86G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895675 | |||||||
| chr16:71895729 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-16+140G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895729 | |||||||
| chr16:71895748 | C | T | 13 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0280 others(10): Show |
15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+159C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895748 | |||||||
| chr16:71895860 | C | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-16+271C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895860 | |||||||
| chr16:71895956 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-16+367C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895956 | |||||||
| chr16:71895992 | A | T | 2 | a0002c0002t0002g0183 a0002c0002t0002g0184 |
2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-16+403A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71895992 | |||||||
| chr16:71896094 | G | C | 16 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(13): Show |
18 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-16+505G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896094 | |||||||
| chr16:71896137 | G | T | 1 | a0003c0004t0027g0078 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-16+548G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896137 | |||||||
| chr16:71896202 | C | A | 7 | a0002c0003t0007g0008 a0002c0003t0007g0080 a0002c0003t0007g0081 others(4): Show |
8 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+613C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896202 | |||||||
| chr16:71896230 | G | T | 2 | a0002c0002t0002g0181 a0002c0002t0002g0182 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-16+641G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896230 | |||||||
| chr16:71896579 | C | G | 1 | a0001c0001t0005g0279 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-16+990C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896579 | |||||||
| chr16:71896904 | A | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-16+1315A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71896904 | |||||||
| chr16:71896975 | G | GA | 256 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(253): Show |
304 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(301): Show |
intron_variant | MODIFIER | c.-16+1397dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71896975 | ||||||
| chr16:71897008 | T | C | 6 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0085 others(3): Show |
8 | HG00738.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+1419T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897008 | |||||||
| chr16:71897129 | C | T | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(224): Show |
270 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.-16+1540C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897129 | |||||||
| chr16:71897172 | C | CT | 11 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0276 others(8): Show |
11 | HG00735.hp1 HG01109.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+1603dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71897172 | ||||||
| chr16:71897172 | CT | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(198): Show |
246 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.-16+1603delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71897172 | ||||||
| chr16:71897185 | T | C | 1 | a0001c0001t0015g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+1596T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897185 | |||||||
| chr16:71897204 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-16+1615G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897204 | |||||||
| chr16:71897223 | T | A | 1 | a0002c0005t0002g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-16+1634T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897223 | |||||||
| chr16:71897223 | T | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(171): Show |
211 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-16+1634T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897223 | |||||||
| chr16:71897316 | G | A | 227 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(224): Show |
270 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.-16+1727G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897316 | |||||||
| chr16:71897324 | G | C | 1 | a0001c0001t0001g0024 | 2 | HG02615.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-16+1735G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897324 | |||||||
| chr16:71897330 | C | T | 1 | a0001c0001t0005g0279 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-16+1741C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897330 | |||||||
| chr16:71897382 | T | C | 1 | a0001c0001t0015g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+1793T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897382 | |||||||
| chr16:71897632 | G | A | 33 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0029 others(30): Show |
38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.-16+2043G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897632 | |||||||
| chr16:71897674 | G | A | 1 | a0001c0001t0004g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-16+2085G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897674 | |||||||
| chr16:71897701 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-16+2112T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897701 | |||||||
| chr16:71897903 | C | T | 4 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0058 others(1): Show |
4 | HG02071.hp2 NA18941.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+2314C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897903 | |||||||
| chr16:71897940 | A | G | 1 | a0001c0001t0023g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-16+2351A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71897940 | |||||||
| chr16:71898092 | T | C | 18 | a0002c0002t0002g0009 a0002c0002t0002g0104 a0002c0002t0002g0106 others(15): Show |
21 | HG00323.hp1 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-16+2503T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898092 | |||||||
| chr16:71898143 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-16+2554G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898143 | |||||||
| chr16:71898152 | A | G | 1 | a0002c0003t0028g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+2563A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898152 | |||||||
| chr16:71898314 | T | A | 1 | a0001c0001t0003g0280 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-16+2725T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898314 | |||||||
| chr16:71898370 | G | GA | 168 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(165): Show |
205 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.-16+2799dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71898370 | ||||||
| chr16:71898370 | G | GAA | 6 | a0001c0001t0003g0089 a0002c0002t0002g0170 a0002c0002t0002g0171 others(3): Show |
6 | HG01175.hp2 HG02738.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+2798_-16+2799d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71898370 | ||||||
| chr16:71898432 | C | G | 16 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(13): Show |
18 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-16+2843C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898432 | |||||||
| chr16:71898441 | T | C | 1 | a0001c0001t0022g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-16+2852T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898441 | |||||||
| chr16:71898534 | A | G | 1 | a0002c0003t0001g0257 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-16+2945A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898534 | |||||||
| chr16:71898626 | A | G | 7 | a0002c0003t0007g0008 a0002c0003t0007g0080 a0002c0003t0007g0081 others(4): Show |
8 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+3037A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898626 | |||||||
| chr16:71898662 | TA | T | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(249): Show |
300 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.-16+3089delA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71898662 | ||||||
| chr16:71898674 | A | C | 1 | a0002c0003t0028g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+3085A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898674 | |||||||
| chr16:71898681 | A | T | 1 | a0002c0003t0001g0257 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-16+3092A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898681 | |||||||
| chr16:71898736 | T | A | 1 | a0003c0004t0006g0065 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-16+3147T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898736 | |||||||
| chr16:71898771 | G | A | 6 | a0001c0001t0003g0089 a0001c0001t0003g0090 a0001c0001t0003g0091 others(3): Show |
6 | HG01884.hp2 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+3182G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898771 | |||||||
| chr16:71898808 | C | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG03017.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-16+3219C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898808 | |||||||
| chr16:71898834 | G | A | 1 | a0001c0001t0015g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+3245G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898834 | |||||||
| chr16:71898897 | G | A | 1 | a0001c0001t0005g0148 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-16+3308G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898897 | |||||||
| chr16:71898964 | CA | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-16+3394delA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71898964 | ||||||
| chr16:71898964 | CAA | C | 7 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0256 others(4): Show |
7 | HG01256.hp1 HG01891.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+3393_-16+3394d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71898964 | ||||||
| chr16:71898980 | A | C | 2 | a0001c0001t0001g0252 a0001c0001t0015g0185 |
2 | HG02486.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-16+3391A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71898980 | |||||||
| chr16:71899084 | C | A | 1 | a0002c0003t0028g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+3495C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899084 | |||||||
| chr16:71899188 | T | A | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(229): Show |
277 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.-16+3599T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899188 | |||||||
| chr16:71899310 | G | A | 1 | a0003c0004t0027g0078 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-16+3721G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899310 | |||||||
| chr16:71899349 | C | T | 1 | a0002c0002t0002g0144 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-16+3760C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899349 | |||||||
| chr16:71899744 | C | G | 3 | a0001c0001t0004g0013 a0001c0001t0004g0053 a0001c0001t0030g0013 |
3 | HG00099.hp1 HG00639.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-16+4155C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899744 | |||||||
| chr16:71899913 | C | T | 2 | a0002c0003t0001g0260 a0002c0003t0001g0275 |
2 | HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-16+4324C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899913 | |||||||
| chr16:71899915 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | NA18977.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-16+4326C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899915 | |||||||
| chr16:71899938 | A | G | 1 | a0002c0003t0001g0274 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-16+4349A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899938 | |||||||
| chr16:71899980 | G | C | 1 | a0002c0003t0020g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-16+4391G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71899980 | |||||||
| chr16:71899996 | C | CA | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(195): Show |
239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.-16+4427dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71899996 | ||||||
| chr16:71899996 | C | CAA | 16 | a0001c0001t0001g0188 a0001c0001t0001g0196 a0001c0001t0001g0197 others(13): Show |
16 | HG01175.hp1 HG02027.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-16+4426_-16+4427d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71899996 | ||||||
| chr16:71900166 | C | CA | 169 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(166): Show |
206 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.-16+4592dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900166 | ||||||
| chr16:71900166 | CA | C | 19 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0280 others(16): Show |
21 | HG01109.hp1 HG01515.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-16+4592delA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900166 | ||||||
| chr16:71900202 | C | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-16+4613C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900202 | |||||||
| chr16:71900230 | G | A | 5 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+4641G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900230 | |||||||
| chr16:71900327 | C | CT | 78 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0032 others(75): Show |
92 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.-16+4761dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900327 | ||||||
| chr16:71900327 | C | CTT | 27 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0244 others(24): Show |
31 | HG00438.hp1 HG00738.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.-16+4760_-16+4761d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900327 | ||||||
| chr16:71900327 | CT | C | 59 | a0001c0001t0001g0125 a0001c0001t0001g0201 a0001c0001t0001g0261 others(56): Show |
75 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-16+4761delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900327 | ||||||
| chr16:71900327 | CTTTTTTT others(5): Show |
C | 36 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(33): Show |
40 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.-16+4750_-16+4761d others(14): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900327 | ||||||
| chr16:71900516 | A | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-16+4927A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900516 | |||||||
| chr16:71900524 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-16+4935G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900524 | |||||||
| chr16:71900566 | G | C | 6 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0085 others(3): Show |
8 | HG00738.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+4977G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900566 | |||||||
| chr16:71900673 | A | ATT | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(256): Show |
307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-16+5085_-16+5086i others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71900673 | ||||||
| chr16:71900673 | A | T | 1 | a0001c0001t0015g0185 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+5084A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900673 | |||||||
| chr16:71900695 | G | A | 1 | a0002c0002t0002g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-16+5106G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900695 | |||||||
| chr16:71900748 | T | C | 1 | a0001c0001t0005g0279 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-16+5159T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900748 | |||||||
| chr16:71900790 | C | T | 5 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+5201C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71900790 | |||||||
| chr16:71901307 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(223): Show |
269 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.-16+5718G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901307 | |||||||
| chr16:71901434 | C | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0192 a0001c0001t0001g0193 others(5): Show |
9 | HG00408.hp2 HG00621.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+5845C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901434 | |||||||
| chr16:71901435 | G | T | 1 | a0001c0001t0001g0195 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-16+5846G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901435 | |||||||
| chr16:71901511 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-16+5922C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901511 | |||||||
| chr16:71901529 | A | T | 6 | a0002c0003t0003g0016 a0002c0003t0003g0094 a0002c0003t0003g0096 others(3): Show |
7 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+5940A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901529 | |||||||
| chr16:71901562 | G | C | 20 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0085 others(17): Show |
23 | HG00738.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-16+5973G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901562 | |||||||
| chr16:71901636 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-16+6047C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901636 | |||||||
| chr16:71901691 | T | C | 3 | a0001c0001t0022g0147 a0001c0001t0023g0165 a0002c0003t0028g0031 |
3 | HG01891.hp2 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-16+6102T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901691 | |||||||
| chr16:71901698 | G | T | 1 | a0002c0003t0028g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+6109G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901698 | |||||||
| chr16:71901919 | A | G | 1 | a0001c0001t0011g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-16+6330A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71901919 | |||||||
| chr16:71902126 | A | G | 2 | a0002c0002t0002g0009 a0002c0002t0002g0109 |
4 | HG02523.hp1 NA18948.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+6537A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902126 | |||||||
| chr16:71902246 | T | C | 1 | a0002c0002t0002g0117 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-16+6657T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902246 | |||||||
| chr16:71902271 | T | G | 3 | a0001c0001t0005g0149 a0001c0001t0005g0150 a0001c0001t0024g0151 |
3 | HG00609.hp1 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-16+6682T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902271 | |||||||
| chr16:71902339 | G | A | 4 | a0001c0001t0003g0282 a0001c0001t0003g0283 a0001c0001t0003g0286 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+6750G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902339 | |||||||
| chr16:71902350 | A | G | 69 | a0001c0001t0001g0125 a0002c0002t0002g0001 a0002c0002t0002g0003 others(66): Show |
86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-16+6761A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902350 | |||||||
| chr16:71902476 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-16+6887G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902476 | |||||||
| chr16:71902540 | G | T | 1 | a0003c0004t0027g0078 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-16+6951G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902540 | |||||||
| chr16:71902559 | C | T | 1 | a0001c0001t0005g0164 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-16+6970C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902559 | |||||||
| chr16:71902571 | A | T | 4 | a0001c0001t0005g0149 a0001c0001t0005g0150 a0001c0001t0005g0163 others(1): Show |
4 | HG00609.hp1 NA18964.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+6982A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902571 | |||||||
| chr16:71902578 | A | G | 16 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(13): Show |
18 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-16+6989A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902578 | |||||||
| chr16:71902678 | G | T | 1 | a0001c0001t0005g0279 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-16+7089G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902678 | |||||||
| chr16:71902743 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0223 |
3 | HG00741.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-16+7154C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902743 | |||||||
| chr16:71902830 | A | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(172): Show |
212 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.-16+7241A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71902830 | |||||||
| chr16:71903028 | T | A | 10 | a0003c0004t0006g0007 a0003c0004t0006g0065 a0003c0004t0006g0067 others(7): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-16+7439T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903028 | |||||||
| chr16:71903332 | C | T | 2 | a0002c0003t0007g0081 a0002c0003t0029g0082 |
2 | HG00733.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-16+7743C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903332 | |||||||
| chr16:71903370 | T | A | 143 | a0001c0001t0001g0125 a0001c0001t0003g0014 a0001c0001t0003g0015 others(140): Show |
170 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.-16+7781T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903370 | |||||||
| chr16:71903372 | T | A | 1 | a0002c0002t0002g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-16+7783T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903372 | |||||||
| chr16:71903381 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-16+7792G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903381 | |||||||
| chr16:71903593 | C | T | 1 | a0002c0002t0002g0109 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-16+8004C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903593 | |||||||
| chr16:71903652 | G | A | 1 | a0002c0002t0002g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-16+8063G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903652 | |||||||
| chr16:71903819 | G | C | 1 | a0002c0003t0001g0227 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-16+8230G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71903819 | |||||||
| chr16:71904014 | T | A | 3 | a0001c0001t0005g0164 a0001c0001t0025g0153 a0002c0003t0005g0152 |
3 | HG04204.hp1 NA18971.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-16+8425T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904014 | |||||||
| chr16:71904211 | C | T | 1 | a0002c0002t0002g0136 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-16+8622C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904211 | |||||||
| chr16:71904421 | C | T | 1 | a0001c0001t0025g0153 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-16+8832C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904421 | |||||||
| chr16:71904423 | G | A | 1 | a0002c0002t0002g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-16+8834G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904423 | |||||||
| chr16:71904438 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-16+8849G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904438 | |||||||
| chr16:71904469 | C | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(100): Show |
123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-16+8880C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904469 | |||||||
| chr16:71904539 | G | A | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(222): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.-16+8950G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904539 | |||||||
| chr16:71904684 | C | T | 2 | a0001c0001t0003g0289 a0001c0001t0003g0290 |
2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-16+9095C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904684 | |||||||
| chr16:71904743 | C | G | 1 | a0001c0001t0004g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-16+9154C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904743 | |||||||
| chr16:71904926 | T | C | 1 | a0002c0002t0002g0120 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-16+9337T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904926 | |||||||
| chr16:71904936 | G | A | 1 | a0002c0003t0005g0152 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-16+9347G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71904936 | |||||||
| chr16:71905007 | T | A | 3 | a0001c0001t0001g0219 a0002c0003t0001g0260 a0002c0003t0001g0275 |
3 | HG01981.hp1 HG02738.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-16+9418T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905007 | |||||||
| chr16:71905163 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-16+9574G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905163 | |||||||
| chr16:71905251 | G | T | 5 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+9662G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905251 | |||||||
| chr16:71905292 | C | T | 5 | a0001c0001t0003g0089 a0001c0001t0003g0090 a0001c0001t0003g0091 others(2): Show |
5 | HG01884.hp2 HG02965.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-16+9703C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905292 | |||||||
| chr16:71905333 | C | T | 1 | a0002c0002t0002g0136 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-16+9744C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905333 | |||||||
| chr16:71905402 | C | CAG | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.-16+9814_-16+9815d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71905402 | ||||||
| chr16:71905410 | C | G | 1 | a0002c0003t0005g0152 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-16+9821C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905410 | |||||||
| chr16:71905417 | T | A | 1 | a0001c0001t0001g0250 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-16+9828T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905417 | |||||||
| chr16:71905610 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-15-10016C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905610 | |||||||
| chr16:71905778 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-15-9848C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905778 | |||||||
| chr16:71905892 | A | T | 1 | a0001c0001t0005g0162 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-15-9734A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905892 | |||||||
| chr16:71905958 | C | G | 1 | a0002c0003t0028g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-15-9668C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71905958 | |||||||
| chr16:71906002 | C | CT | 11 | a0001c0001t0001g0037 a0001c0001t0001g0246 a0001c0001t0003g0014 others(8): Show |
13 | HG00738.hp1 HG01496.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15-9606dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71906002 | ||||||
| chr16:71906002 | C | CTT | 69 | a0001c0001t0001g0125 a0001c0001t0001g0242 a0002c0002t0002g0001 others(66): Show |
86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-15-9607_-15-9606d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71906002 | ||||||
| chr16:71906053 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-15-9573G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906053 | |||||||
| chr16:71906108 | A | T | 1 | a0001c0001t0003g0088 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-15-9518A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906108 | |||||||
| chr16:71906128 | C | G | 1 | a0002c0003t0008g0222 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-15-9498C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906128 | |||||||
| chr16:71906128 | C | T | 1 | a0002c0002t0002g0136 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-15-9498C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906128 | |||||||
| chr16:71906144 | C | T | 1 | a0001c0001t0022g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15-9482C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906144 | |||||||
| chr16:71906161 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-15-9465G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906161 | |||||||
| chr16:71906193 | C | T | 2 | a0002c0002t0002g0183 a0002c0002t0002g0184 |
2 | HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-15-9433C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906193 | |||||||
| chr16:71906348 | C | T | 6 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0085 others(3): Show |
8 | HG00738.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-9278C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906348 | |||||||
| chr16:71906411 | G | C | 2 | a0002c0002t0002g0122 a0002c0002t0002g0173 |
2 | NA18983.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-15-9215G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906411 | |||||||
| chr16:71906922 | T | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(256): Show |
307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-15-8704T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71906922 | |||||||
| chr16:71907037 | A | T | 1 | a0002c0003t0001g0045 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-15-8589A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907037 | |||||||
| chr16:71907187 | CT | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(199): Show |
243 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.-15-8425delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71907187 | ||||||
| chr16:71907187 | CTT | C | 6 | a0001c0001t0001g0210 a0001c0001t0001g0233 a0001c0001t0001g0277 others(3): Show |
6 | HG03490.hp2 NA18950.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-8426_-15-8425d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71907187 | ||||||
| chr16:71907280 | A | AT | 38 | a0001c0001t0001g0063 a0001c0001t0001g0241 a0001c0001t0003g0014 others(35): Show |
43 | HG00738.hp1 HG01081.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.-15-8331dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71907280 | ||||||
| chr16:71907356 | C | T | 52 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(49): Show |
58 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-15-8270C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907356 | |||||||
| chr16:71907379 | G | A | 6 | a0002c0002t0002g0116 a0002c0002t0002g0121 a0002c0002t0002g0123 others(3): Show |
6 | HG02698.hp1 HG02735.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-8247G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907379 | |||||||
| chr16:71907523 | C | T | 4 | a0001c0001t0003g0030 a0001c0001t0003g0281 a0001c0001t0003g0284 others(1): Show |
5 | HG02109.hp1 HG02486.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-8103C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907523 | |||||||
| chr16:71907554 | G | T | 3 | a0001c0001t0004g0013 a0001c0001t0004g0053 a0001c0001t0030g0013 |
3 | HG00099.hp1 HG00639.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-15-8072G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907554 | |||||||
| chr16:71907563 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-15-8063C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907563 | |||||||
| chr16:71907733 | T | A | 6 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(3): Show |
6 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-7893T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907733 | |||||||
| chr16:71907795 | A | T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-15-7831A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907795 | |||||||
| chr16:71907847 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-15-7779C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907847 | |||||||
| chr16:71907883 | G | A | 16 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(13): Show |
18 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15-7743G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907883 | |||||||
| chr16:71907896 | C | G | 16 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(13): Show |
18 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15-7730C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907896 | |||||||
| chr16:71907965 | A | T | 1 | a0002c0003t0007g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15-7661A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907965 | |||||||
| chr16:71907966 | G | T | 1 | a0002c0003t0007g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-15-7660G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907966 | |||||||
| chr16:71907994 | G | A | 1 | a0002c0002t0002g0116 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-15-7632G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71907994 | |||||||
| chr16:71908005 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-15-7621T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908005 | |||||||
| chr16:71908009 | A | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(204): Show |
249 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.-15-7617A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908009 | |||||||
| chr16:71908027 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-15-7599G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908027 | |||||||
| chr16:71908051 | T | G | 1 | a0002c0003t0020g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-15-7575T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908051 | |||||||
| chr16:71908126 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-15-7500T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908126 | |||||||
| chr16:71908158 | G | A | 1 | a0002c0003t0020g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-15-7468G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908158 | |||||||
| chr16:71908296 | C | CT | 68 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(65): Show |
87 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.-15-7308dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | ||||||
| chr16:71908296 | C | CTT | 137 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0125 others(134): Show |
163 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.-15-7309_-15-7308d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | ||||||
| chr16:71908296 | C | CTTT | 20 | a0001c0001t0001g0191 a0001c0001t0001g0220 a0001c0001t0001g0221 others(17): Show |
20 | HG01109.hp1 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-7310_-15-7308d others(5): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | ||||||
| chr16:71908296 | C | CTTTT | 30 | a0001c0001t0001g0238 a0001c0001t0005g0019 a0001c0001t0005g0021 others(27): Show |
34 | HG00140.hp1 HG00423.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.-15-7311_-15-7308d others(6): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | ||||||
| chr16:71908296 | C | CTTTTT | 7 | a0001c0001t0005g0150 a0001c0001t0005g0160 a0001c0001t0005g0161 others(4): Show |
7 | HG00609.hp1 HG00733.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-7312_-15-7308d others(7): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | ||||||
| chr16:71908296 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0063 a0001c0007t0001g0054 |
4 | HG02055.hp2 HG02717.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-7318_-15-7308d others(13): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71908296 | ||||||
| chr16:71908328 | C | G | 1 | a0002c0003t0007g0177 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-15-7298C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908328 | |||||||
| chr16:71908373 | C | A | 1 | a0001c0001t0022g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15-7253C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908373 | |||||||
| chr16:71908403 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.-15-7223G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908403 | |||||||
| chr16:71908527 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-15-7099C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908527 | |||||||
| chr16:71908536 | C | T | 33 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0029 others(30): Show |
38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-7090C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908536 | |||||||
| chr16:71908685 | A | C | 13 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0280 others(10): Show |
15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15-6941A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908685 | |||||||
| chr16:71908711 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-15-6915T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908711 | |||||||
| chr16:71908746 | G | T | 7 | a0002c0002t0002g0003 a0002c0002t0002g0114 a0002c0002t0002g0115 others(4): Show |
11 | NA18949.hp2 NA18951.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-6880G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71908746 | |||||||
| chr16:71909095 | C | CT | 40 | a0001c0001t0001g0063 a0001c0001t0001g0252 a0001c0001t0003g0029 others(37): Show |
44 | HG01070.hp1 HG01071.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-15-6511dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71909095 | ||||||
| chr16:71909095 | C | CTT | 25 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0200 others(22): Show |
28 | HG00738.hp1 HG01433.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.-15-6512_-15-6511d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71909095 | ||||||
| chr16:71909095 | C | CTTTT | 71 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(68): Show |
90 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-15-6514_-15-6511d others(6): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71909095 | ||||||
| chr16:71909095 | C | CTTTTT | 15 | a0001c0001t0001g0186 a0001c0001t0001g0193 a0001c0001t0001g0203 others(12): Show |
15 | HG00609.hp2 HG00741.hp2 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15-6515_-15-6511d others(7): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71909095 | ||||||
| chr16:71909204 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-15-6422T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909204 | |||||||
| chr16:71909266 | G | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-15-6360G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909266 | |||||||
| chr16:71909355 | C | T | 2 | a0002c0002t0002g0132 a0002c0002t0002g0179 |
2 | NA18946.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-15-6271C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909355 | |||||||
| chr16:71909406 | C | T | 34 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(31): Show |
38 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-6220C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909406 | |||||||
| chr16:71909511 | C | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(256): Show |
307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.-15-6115C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909511 | |||||||
| chr16:71909608 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-15-6018A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909608 | |||||||
| chr16:71909653 | A | G | 68 | a0001c0001t0001g0125 a0002c0002t0002g0001 a0002c0002t0002g0003 others(65): Show |
85 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-15-5973A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909653 | |||||||
| chr16:71909691 | C | T | 33 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0029 others(30): Show |
38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-5935C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909691 | |||||||
| chr16:71909878 | C | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(100): Show |
123 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-15-5748C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909878 | |||||||
| chr16:71909965 | C | T | 7 | a0002c0002t0002g0116 a0002c0002t0002g0121 a0002c0002t0002g0123 others(4): Show |
7 | HG02165.hp1 HG02698.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-5661C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71909965 | |||||||
| chr16:71910037 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-15-5589T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910037 | |||||||
| chr16:71910044 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-15-5582A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910044 | |||||||
| chr16:71910094 | T | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0200 others(12): Show |
16 | HG01433.hp1 HG02257.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15-5532T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910094 | |||||||
| chr16:71910124 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-15-5502G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910124 | |||||||
| chr16:71910168 | G | A | 10 | a0003c0004t0006g0007 a0003c0004t0006g0065 a0003c0004t0006g0067 others(7): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15-5458G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910168 | |||||||
| chr16:71910322 | A | G | 3 | a0003c0004t0006g0065 a0003c0004t0006g0069 a0003c0004t0027g0078 |
3 | HG03130.hp1 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-15-5304A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910322 | |||||||
| chr16:71910377 | C | T | 1 | a0001c0001t0022g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-15-5249C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910377 | |||||||
| chr16:71910561 | G | T | 1 | a0002c0002t0002g0107 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-15-5065G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910561 | |||||||
| chr16:71910605 | C | CA | 33 | a0001c0001t0003g0282 a0001c0001t0005g0019 a0001c0001t0005g0021 others(30): Show |
37 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.-15-5008dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71910605 | ||||||
| chr16:71910763 | A | T | 10 | a0003c0004t0006g0007 a0003c0004t0006g0065 a0003c0004t0006g0067 others(7): Show |
12 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15-4863A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910763 | |||||||
| chr16:71910828 | GA | G | 20 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0085 others(17): Show |
23 | HG00738.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15-4794delA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71910828 | ||||||
| chr16:71910943 | T | G | 1 | a0002c0002t0002g0146 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-15-4683T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910943 | |||||||
| chr16:71910989 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15-4637A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71910989 | |||||||
| chr16:71911008 | G | A | 3 | a0001c0001t0004g0033 a0001c0001t0004g0046 a0001c0001t0004g0061 |
3 | HG00642.hp1 HG00738.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.-15-4618G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911008 | |||||||
| chr16:71911045 | G | T | 1 | a0001c0001t0001g0251 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15-4581G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911045 | |||||||
| chr16:71911069 | G | A | 4 | a0001c0001t0001g0063 a0002c0002t0002g0023 a0002c0002t0002g0140 others(1): Show |
5 | HG03098.hp1 NA18943.hp1 NA19064.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-4557G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911069 | |||||||
| chr16:71911089 | A | G | 1 | a0003c0004t0006g0070 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15-4537A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911089 | |||||||
| chr16:71911219 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-15-4407T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911219 | |||||||
| chr16:71911264 | C | T | 1 | a0002c0003t0020g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-15-4362C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911264 | |||||||
| chr16:71911344 | A | T | 1 | a0001c0001t0005g0161 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-15-4282A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911344 | |||||||
| chr16:71911358 | T | A | 2 | a0002c0002t0002g0141 a0002c0002t0002g0170 |
2 | NA19072.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-15-4268T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911358 | |||||||
| chr16:71911358 | T | TA | 247 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(244): Show |
294 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.-15-4260dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911358 | ||||||
| chr16:71911366 | A | AC | 6 | a0001c0001t0003g0089 a0001c0001t0003g0090 a0001c0001t0003g0091 others(3): Show |
6 | HG01884.hp2 HG02965.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-4259dupC | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911366 | ||||||
| chr16:71911375 | A | G | 36 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(33): Show |
40 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.-15-4251A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911375 | |||||||
| chr16:71911438 | C | G | 20 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0033 others(17): Show |
23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15-4188C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911438 | |||||||
| chr16:71911710 | A | AT | 8 | a0001c0001t0001g0037 a0001c0001t0003g0086 a0001c0001t0003g0090 others(5): Show |
8 | HG00735.hp1 HG01361.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-3892dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911710 | ||||||
| chr16:71911710 | AT | A | 31 | a0001c0001t0001g0063 a0001c0001t0001g0234 a0001c0001t0001g0252 others(28): Show |
35 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.-15-3892delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911710 | ||||||
| chr16:71911710 | ATT | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(194): Show |
238 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.-15-3893_-15-3892d others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911710 | ||||||
| chr16:71911710 | ATTT | A | 6 | a0001c0001t0001g0251 a0001c0001t0001g0256 a0001c0001t0005g0154 others(3): Show |
6 | HG00639.hp1 HG01169.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-3894_-15-3892d others(5): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71911710 | ||||||
| chr16:71911874 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-15-3752G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911874 | |||||||
| chr16:71911944 | G | C | 51 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(48): Show |
57 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.-15-3682G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71911944 | |||||||
| chr16:71912000 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-15-3626C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912000 | |||||||
| chr16:71912214 | T | G | 1 | a0001c0001t0001g0226 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-15-3412T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912214 | |||||||
| chr16:71912486 | C | G | 20 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0033 others(17): Show |
23 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15-3140C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912486 | |||||||
| chr16:71912526 | C | T | 5 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-3100C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912526 | |||||||
| chr16:71912635 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-15-2991A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912635 | |||||||
| chr16:71912647 | G | A | 4 | a0001c0001t0004g0056 a0001c0001t0004g0057 a0001c0001t0004g0058 others(1): Show |
4 | HG02071.hp2 NA18941.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-2979G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912647 | |||||||
| chr16:71912775 | G | A | 1 | a0002c0002t0002g0117 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-15-2851G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71912775 | |||||||
| chr16:71913278 | C | CT | 17 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(14): Show |
19 | HG01515.hp1 HG01891.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-15-2337dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71913278 | ||||||
| chr16:71913388 | T | C | 1 | a0001c0001t0004g0061 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-15-2238T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913388 | |||||||
| chr16:71913435 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-15-2191C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913435 | |||||||
| chr16:71913777 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-15-1849A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913777 | |||||||
| chr16:71913831 | G | A | 35 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(32): Show |
39 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.-15-1795G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913831 | |||||||
| chr16:71913894 | C | T | 3 | a0001c0001t0022g0147 a0001c0001t0023g0165 a0002c0003t0028g0031 |
3 | HG01891.hp2 HG02451.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-15-1732C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913894 | |||||||
| chr16:71913965 | C | T | 20 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0085 others(17): Show |
23 | HG00738.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15-1661C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71913965 | |||||||
| chr16:71914100 | G | A | 69 | a0001c0010t0001g0216 a0002c0002t0002g0001 a0002c0002t0002g0003 others(66): Show |
86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-15-1526G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914100 | |||||||
| chr16:71914115 | G | GTTGT | 258 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.-15-1505_-15-1502d others(6): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71914115 | ||||||
| chr16:71914138 | A | G | 20 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0085 others(17): Show |
23 | HG00738.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-15-1488A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914138 | |||||||
| chr16:71914140 | T | C | 69 | a0001c0010t0001g0216 a0002c0002t0002g0001 a0002c0002t0002g0003 others(66): Show |
86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-15-1486T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914140 | |||||||
| chr16:71914170 | C | CT | 18 | a0001c0001t0001g0006 a0001c0001t0001g0042 a0001c0001t0001g0043 others(15): Show |
20 | HG00099.hp2 HG00621.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-1440dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 71914170 | ||||||
| chr16:71914392 | C | T | 1 | a0001c0001t0004g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-15-1234C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914392 | |||||||
| chr16:71914452 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15-1174A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914452 | |||||||
| chr16:71914582 | G | C | 1 | a0001c0001t0004g0033 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-15-1044G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914582 | |||||||
| chr16:71914731 | T | C | 1 | a0002c0002t0002g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-15-895T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914731 | |||||||
| chr16:71914990 | T | C | 5 | a0002c0002t0002g0107 a0002c0005t0002g0017 a0002c0005t0002g0102 others(2): Show |
6 | HG00323.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-636T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71914990 | |||||||
| chr16:71915260 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(102): Show |
125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.-15-366C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71915260 | |||||||
| chr16:71915363 | C | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(171): Show |
211 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.-15-263C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71915363 | |||||||
| chr16:71915387 | C | G | 1 | a0002c0002t0002g0172 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-15-239C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71915387 | |||||||
| chr16:71915538 | T | A | 6 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(3): Show |
6 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-88T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 1/9 | chr16 | 71915538 | |||||||
| chr16:71915951 | C | T | 1 | a0001c0001t0008g0211 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.88+223C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71915951 | |||||||
| chr16:71916127 | C | T | 1 | a0002c0002t0002g0104 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.89-335C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71916127 | |||||||
| chr16:71916298 | A | G | 24 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(21): Show |
27 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.89-164A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71916298 | |||||||
| chr16:71916390 | G | A | 30 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(27): Show |
34 | HG00140.hp1 HG01074.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.89-72G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71916390 | |||||||
| chr16:71916390 | G | C | 1 | a0002c0003t0001g0213 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.89-72G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71916390 | |||||||
| chr16:71916419 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.89-43A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 2/9 | chr16 | 71916419 | |||||||
| chr16:71916736 | C | CCCAA | 6 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(3): Show |
6 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.269+95_269+98dupCC others(2): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr16 | 71916736 | ||||||
| chr16:71916989 | G | A | 13 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0280 others(10): Show |
15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.270-58G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 3/9 | chr16 | 71916989 | |||||||
| chr16:71917191 | G | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(98): Show |
121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.357+57G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917191 | |||||||
| chr16:71917194 | A | G | 1 | a0002c0002t0002g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.357+60A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917194 | |||||||
| chr16:71917205 | C | A | 1 | a0002c0002t0002g0183 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.357+71C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917205 | |||||||
| chr16:71917303 | T | TAGAAC | 3 | a0001c0001t0001g0206 a0001c0001t0001g0229 a0001c0001t0001g0251 |
3 | HG00140.hp2 HG02735.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.357+172_357+176dup others(5): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 71917303 | ||||||
| chr16:71917345 | A | C | 13 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0280 others(10): Show |
15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.357+211A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917345 | |||||||
| chr16:71917454 | G | C | 5 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.357+320G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917454 | |||||||
| chr16:71917454 | G | T | 14 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0200 others(11): Show |
15 | HG01433.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.357+320G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917454 | |||||||
| chr16:71917638 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.357+504G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917638 | |||||||
| chr16:71917942 | A | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
230 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.357+808A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917942 | |||||||
| chr16:71917969 | T | C | 4 | a0002c0003t0001g0227 a0002c0003t0001g0231 a0002c0003t0001g0260 others(1): Show |
4 | HG01243.hp1 HG02698.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+835T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71917969 | |||||||
| chr16:71918014 | G | A | 4 | a0001c0001t0004g0012 a0001c0001t0004g0044 a0001c0001t0004g0050 others(1): Show |
5 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.357+880G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918014 | |||||||
| chr16:71918041 | G | C | 1 | a0005c0008t0001g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.357+907G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918041 | |||||||
| chr16:71918214 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.357+1080A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918214 | |||||||
| chr16:71918340 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0218 a0001c0001t0019g0198 |
4 | HG00408.hp1 HG02027.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+1206A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918340 | |||||||
| chr16:71918417 | CT | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(259): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.357+1300delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 71918417 | ||||||
| chr16:71918451 | G | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(222): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.357+1317G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918451 | |||||||
| chr16:71918606 | C | T | 23 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(20): Show |
25 | HG00140.hp1 HG01168.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.357+1472C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918606 | |||||||
| chr16:71918668 | G | A | 1 | a0001c0001t0004g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.357+1534G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918668 | |||||||
| chr16:71918711 | G | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(250): Show |
301 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.357+1577G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918711 | |||||||
| chr16:71918828 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.357+1694C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71918828 | |||||||
| chr16:71919119 | G | A | 48 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(45): Show |
54 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.358-1620G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919119 | |||||||
| chr16:71919153 | G | C | 1 | a0001c0001t0023g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-1586G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919153 | |||||||
| chr16:71919226 | T | G | 1 | a0001c0001t0001g0241 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.358-1513T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919226 | |||||||
| chr16:71919334 | GTTTTC | G | 35 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(32): Show |
39 | HG00140.hp1 HG00733.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.358-1399_358-1395d others(7): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 71919334 | ||||||
| chr16:71919404 | G | C | 1 | a0001c0001t0001g0201 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.358-1335G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919404 | |||||||
| chr16:71919446 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.358-1293C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919446 | |||||||
| chr16:71919468 | C | T | 1 | a0002c0002t0002g0108 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.358-1271C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919468 | |||||||
| chr16:71919722 | C | T | 2 | a0001c0001t0012g0066 a0001c0001t0012g0074 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.358-1017C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919722 | |||||||
| chr16:71919819 | T | C | 1 | a0002c0002t0002g0127 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.358-920T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919819 | |||||||
| chr16:71919938 | T | G | 13 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0280 others(10): Show |
15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.358-801T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919938 | |||||||
| chr16:71919981 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.358-758G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71919981 | |||||||
| chr16:71920257 | A | C | 1 | a0001c0001t0003g0015 | 2 | HG00738.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.358-482A>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920257 | |||||||
| chr16:71920310 | A | G | 1 | a0002c0002t0002g0124 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.358-429A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920310 | |||||||
| chr16:71920416 | CAA | C | 13 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0280 others(10): Show |
15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.358-322_358-321del others(2): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920416 | |||||||
| chr16:71920433 | A | G | 2 | a0001c0001t0005g0154 a0001c0001t0005g0158 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.358-306A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920433 | |||||||
| chr16:71920545 | C | A | 2 | a0001c0001t0003g0095 a0001c0001t0003g0101 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.358-194C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920545 | |||||||
| chr16:71920547 | C | T | 5 | a0001c0001t0011g0073 a0001c0001t0011g0075 a0001c0001t0011g0076 others(2): Show |
5 | HG01515.hp1 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-192C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920547 | |||||||
| chr16:71920630 | G | A | 1 | a0001c0001t0023g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.358-109G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 4/9 | chr16 | 71920630 | |||||||
| chr16:71920880 | C | G | 1 | a0001c0001t0001g0209 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.441+58C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 5/9 | chr16 | 71920880 | |||||||
| chr16:71920922 | G | T | 9 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0085 others(6): Show |
12 | HG00738.hp1 HG01884.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+100G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 5/9 | chr16 | 71920922 | |||||||
| chr16:71920978 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0199 others(1): Show |
4 | HG02071.hp1 HG02165.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+156C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 5/9 | chr16 | 71920978 | |||||||
| chr16:71921182 | C | T | 69 | a0002c0002t0002g0001 a0002c0002t0002g0003 a0002c0002t0002g0009 others(66): Show |
86 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.442-161C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 5/9 | chr16 | 71921182 | |||||||
| chr16:71921336 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA19086.hp1 | splice_region_variant&intron_variant | LOW | c.442-7C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 5/9 | chr16 | 71921336 | |||||||
| chr16:71921497 | T | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
230 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.552+44T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71921497 | |||||||
| chr16:71921523 | C | CAT | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
308 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.552+71_552+72dupAT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr16 | 71921523 | ||||||
| chr16:71921769 | C | G | 1 | a0001c0001t0022g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.552+316C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71921769 | |||||||
| chr16:71921892 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.552+439C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71921892 | |||||||
| chr16:71921954 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.552+501G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71921954 | |||||||
| chr16:71921980 | A | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0199 others(1): Show |
4 | HG02071.hp1 HG02165.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.553-494A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71921980 | |||||||
| chr16:71922187 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.553-287G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 6/9 | chr16 | 71922187 | |||||||
| chr16:71922685 | GTATA | G | 72 | a0001c0001t0001g0252 a0001c0001t0015g0185 a0002c0002t0002g0001 others(69): Show |
89 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.759+10_759+13delTA others(2): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr16 | 71922685 | ||||||
| chr16:71922689 | A | AAGTGTG | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(101): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.759+9_759+10insAGT others(3): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922689 | |||||||
| chr16:71922690 | T | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(101): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.759+10T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922690 | |||||||
| chr16:71922693 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(101): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.759+13A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922693 | |||||||
| chr16:71922694 | A | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(101): Show |
124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.759+14A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922694 | |||||||
| chr16:71922800 | A | G | 1 | a0002c0002t0002g0118 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.759+120A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922800 | |||||||
| chr16:71922831 | C | G | 3 | a0001c0001t0010g0020 a0001c0001t0010g0157 a0002c0003t0010g0020 |
3 | HG01358.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.759+151C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71922831 | |||||||
| chr16:71923068 | G | T | 1 | a0001c0001t0023g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.760-220G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 7/9 | chr16 | 71923068 | |||||||
| chr16:71923578 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.852+198A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71923578 | |||||||
| chr16:71923784 | AGATT | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0214 |
3 | HG02615.hp2 HG02895.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.852+408_852+411del others(4): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr16 | 71923784 | ||||||
| chr16:71923821 | G | A | 1 | a0005c0008t0001g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.852+441G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71923821 | |||||||
| chr16:71923822 | C | A | 1 | a0005c0008t0001g0240 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.852+442C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71923822 | |||||||
| chr16:71923823 | C | T | 2 | a0002c0002t0002g0106 a0002c0002t0002g0112 |
2 | NA18959.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.852+443C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71923823 | |||||||
| chr16:71923850 | T | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
126 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.852+470T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71923850 | |||||||
| chr16:71924020 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.852+640A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924020 | |||||||
| chr16:71924040 | T | G | 6 | a0002c0003t0003g0016 a0002c0003t0003g0094 a0002c0003t0003g0096 others(3): Show |
7 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.852+660T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924040 | |||||||
| chr16:71924122 | C | G | 18 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0033 others(15): Show |
21 | HG00642.hp1 HG00735.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.853-647C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924122 | |||||||
| chr16:71924149 | A | G | 52 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(49): Show |
58 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.853-620A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924149 | |||||||
| chr16:71924205 | C | T | 6 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0085 others(3): Show |
8 | HG00738.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.853-564C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924205 | |||||||
| chr16:71924336 | G | A | 13 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0280 others(10): Show |
15 | HG01109.hp1 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.853-433G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924336 | |||||||
| chr16:71924543 | A | G | 1 | a0001c0001t0023g0165 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.853-226A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924543 | |||||||
| chr16:71924662 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.853-107G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 8/9 | chr16 | 71924662 | |||||||
| chr16:71924861 | C | G | 1 | a0001c0001t0004g0048 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.901+44C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71924861 | |||||||
| chr16:71924863 | T | A | 1 | a0001c0001t0001g0207 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.901+46T>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71924863 | |||||||
| chr16:71924877 | A | G | 1 | a0001c0001t0004g0046 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.901+60A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71924877 | |||||||
| chr16:71924942 | T | C | 1 | a0002c0002t0002g0172 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.901+125T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71924942 | |||||||
| chr16:71925011 | A | AT | 36 | a0001c0001t0001g0032 a0001c0001t0001g0197 a0001c0001t0001g0258 others(33): Show |
39 | HG01168.hp1 HG01169.hp2 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.901+213dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71925011 | ||||||
| chr16:71925011 | AT | A | 10 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0042 others(7): Show |
10 | HG00099.hp2 HG01496.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.901+213delT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71925011 | ||||||
| chr16:71925052 | G | T | 1 | a0001c0001t0001g0263 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.901+235G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925052 | |||||||
| chr16:71925059 | C | T | 1 | a0002c0003t0028g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.901+242C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925059 | |||||||
| chr16:71925096 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.901+279T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925096 | |||||||
| chr16:71925097 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.901+280C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925097 | |||||||
| chr16:71925111 | C | T | 1 | a0002c0002t0002g0278 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.901+294C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925111 | |||||||
| chr16:71925175 | G | C | 33 | a0001c0001t0005g0019 a0001c0001t0005g0021 a0001c0001t0005g0148 others(30): Show |
37 | HG00140.hp1 HG00609.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.901+358G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925175 | |||||||
| chr16:71925215 | G | A | 2 | a0002c0002t0002g0181 a0002c0002t0002g0182 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.901+398G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925215 | |||||||
| chr16:71925284 | G | T | 1 | a0002c0002t0002g0173 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.901+467G>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925284 | |||||||
| chr16:71925316 | A | AT | 15 | a0001c0001t0001g0269 a0001c0001t0003g0288 a0001c0001t0004g0035 others(12): Show |
15 | HG00621.hp2 HG01123.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.901+517dupT | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71925316 | ||||||
| chr16:71925316 | A | ATT | 14 | a0001c0001t0001g0024 a0001c0001t0001g0188 a0001c0001t0001g0200 others(11): Show |
15 | HG01433.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.901+516_901+517dup others(2): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71925316 | ||||||
| chr16:71925339 | C | G | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.901+522C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925339 | |||||||
| chr16:71925410 | G | A | 1 | a0002c0003t0001g0249 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.901+593G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925410 | |||||||
| chr16:71925497 | G | A | 1 | a0001c0001t0003g0285 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.901+680G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925497 | |||||||
| chr16:71925699 | TGTA | T | 33 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0029 others(30): Show |
38 | HG00738.hp1 HG01109.hp1 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.901+883_901+885del others(3): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925699 | |||||||
| chr16:71925748 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.901+931A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925748 | |||||||
| chr16:71925758 | G | A | 8 | a0002c0003t0007g0008 a0002c0003t0007g0080 a0002c0003t0007g0081 others(5): Show |
9 | HG00733.hp1 HG01074.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.901+941G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925758 | |||||||
| chr16:71925776 | C | T | 1 | a0001c0001t0004g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.901+959C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925776 | |||||||
| chr16:71925824 | A | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(227): Show |
273 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(270): Show |
intron_variant | MODIFIER | c.901+1007A>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925824 | |||||||
| chr16:71925830 | T | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(259): Show |
310 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.901+1013T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925830 | |||||||
| chr16:71925845 | C | T | 72 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0002c0002t0002g0001 others(69): Show |
89 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.901+1028C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925845 | |||||||
| chr16:71925907 | T | C | 1 | a0001c0010t0001g0216 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.901+1090T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925907 | |||||||
| chr16:71925908 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.901+1091G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925908 | |||||||
| chr16:71925948 | A | T | 1 | a0002c0002t0002g0173 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.901+1131A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71925948 | |||||||
| chr16:71926154 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.901+1337C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926154 | |||||||
| chr16:71926214 | G | A | 1 | a0002c0003t0020g0064 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.901+1397G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926214 | |||||||
| chr16:71926329 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0197 a0001c0001t0001g0258 others(1): Show |
4 | HG00438.hp2 NA18955.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.902-1285T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926329 | |||||||
| chr16:71926346 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.902-1268C>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926346 | |||||||
| chr16:71926347 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.902-1267A>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926347 | |||||||
| chr16:71926348 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.902-1266T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926348 | |||||||
| chr16:71926415 | C | G | 1 | a0002c0002t0002g0172 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.902-1199C>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926415 | |||||||
| chr16:71926539 | G | A | 3 | a0002c0002t0002g0009 a0002c0002t0002g0109 a0002c0002t0002g0166 |
5 | HG02083.hp2 HG02523.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.902-1075G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926539 | |||||||
| chr16:71926710 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.902-904T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926710 | |||||||
| chr16:71926927 | C | T | 1 | a0002c0002t0002g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.902-687C>T | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926927 | |||||||
| chr16:71926983 | T | G | 1 | a0001c0001t0001g0270 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.902-631T>G | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71926983 | |||||||
| chr16:71927343 | G | C | 24 | a0001c0001t0004g0005 a0001c0001t0004g0012 a0001c0001t0004g0013 others(21): Show |
27 | HG00099.hp1 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.902-271G>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71927343 | |||||||
| chr16:71927436 | T | C | 263 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
311 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(308): Show |
intron_variant | MODIFIER | c.902-178T>C | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71927436 | |||||||
| chr16:71927486 | C | CA | 94 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0003g0286 others(91): Show |
113 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.902-112dupA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71927486 | ||||||
| chr16:71927486 | C | CAA | 12 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0280 others(9): Show |
14 | HG01109.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.902-113_902-112dup others(2): Show |
IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71927486 | ||||||
| chr16:71927486 | CA | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(88): Show |
110 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.902-112delA | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr16 | 71927486 | ||||||
| chr16:71927591 | G | A | 1 | a0001c0001t0026g0155 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.902-23G>A | IST1 | ENSG00000182149.21 | transcript | ENST00000378799.11 | protein_coding | 9/9 | chr16 | 71927591 |