Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57508 |
| ensemblid | ENSG00000108506.14 |
| hgncid | 29241 |
| symbol | INTS2 |
| name | integrator complex subunit 2 |
| refseq_nuc | NM_001351695.2 |
| refseq_prot | NP_001338624.2 |
| ensembl_nuc | ENST00000251334.7 |
| ensembl_prot | ENSP00000251334.6 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 61865367 |
| end | 61927982 |
| strand | - |
| ver | v1.2 |
| region | chr17:61865367-61927982 |
| region5000 | chr17:61860367-61932982 |
| regionname0 | INTS2_chr17_61865367_61927982 |
| regionname5000 | INTS2_chr17_61860367_61932982 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1196 | 360 | 84 | 59 | 169 | 12 | 35 | 131 | INTS2_chr17_61860367_61932982 | INTS2 | MTECT others(1191): Show |
chr17 | 61860367 | 61932982 |
| a0002 | 0/0 | 1196 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | MTECT others(1191): Show |
chr17 | 61860367 | 61932982 |
| a0003 | 0/0 | 1196 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | MTECT others(1191): Show |
chr17 | 61860367 | 61932982 |
| a0004 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | MTECT others(1191): Show |
chr17 | 61860367 | 61932982 |
| a0005 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | MTECT others(1191): Show |
chr17 | 61860367 | 61932982 |
| a0006 | 0/0 | 1196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | MTECT others(1191): Show |
chr17 | 61860367 | 61932982 |
| a0007 | 0/1 | 1196 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | MTECT others(1191): Show |
chr17 | 61860367 | 61932982 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3588 | 303 | 79 | 54 | 130 | 12 | 27 | INTS2_chr17_61860367_61932982 | INTS2 | ATGAC others(3583): Show |
chr17 | 61860367 | 61932982 | ||
| a0001c0002 | 0/0 | 3588 | 51 | 1 | 5 | 37 | 0 | 8 | INTS2_chr17_61860367_61932982 | INTS2 | ATGAC others(3583): Show |
chr17 | 61860367 | 61932982 | ||
| a0001c0003 | 0/0 | 3588 | 4 | 4 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | ATGAC others(3583): Show |
chr17 | 61860367 | 61932982 | ||
| a0001c0004 | 0/0 | 3588 | 2 | 0 | 0 | 2 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | ATGAC others(3583): Show |
chr17 | 61860367 | 61932982 | ||
| a0002c0005 | 0/0 | 3588 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | ATGAC others(3583): Show |
chr17 | 61860367 | 61932982 | ||
| a0003c0009 | 0/0 | 3588 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | ATGAC others(3583): Show |
chr17 | 61860367 | 61932982 | ||
| a0004c0006 | 0/0 | 3588 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | ATGAC others(3583): Show |
chr17 | 61860367 | 61932982 | ||
| a0005c0007 | 0/0 | 3588 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | ATGAC others(3583): Show |
chr17 | 61860367 | 61932982 | ||
| a0006c0010 | 0/0 | 3588 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | ATGAC others(3583): Show |
chr17 | 61860367 | 61932982 | ||
| a0007c0008 | 0/1 | 3588 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | ATGAC others(3583): Show |
chr17 | 61860367 | 61932982 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6128 | 98 | 15 | 26 | 41 | 6 | 9 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0002 | 0/0 | 6128 | 89 | 11 | 8 | 65 | 2 | 3 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0003 | 0/0 | 6128 | 75 | 36 | 17 | 12 | 2 | 8 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0004 | 0/0 | 6129 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0005 | 0/0 | 6128 | 7 | 7 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0006 | 0/0 | 6129 | 5 | 0 | 0 | 5 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0007 | 0/0 | 6129 | 5 | 2 | 0 | 3 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0008 | 0/0 | 6128 | 4 | 0 | 0 | 0 | 0 | 4 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0010 | 0/0 | 6129 | 3 | 2 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0012 | 0/0 | 6128 | 2 | 0 | 0 | 0 | 0 | 2 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0013 | 0/0 | 6129 | 2 | 2 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0014 | 0/0 | 6128 | 2 | 2 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0015 | 0/0 | 6128 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0016 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0017 | 0/0 | 6128 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0018 | 0/0 | 6128 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0019 | 0/0 | 6129 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0020 | 0/0 | 6129 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0021 | 0/0 | 6129 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0022 | 0/0 | 6128 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0025 | 0/0 | 6128 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0001t0026 | 0/0 | 6128 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0002t0004 | 0/0 | 6129 | 42 | 1 | 5 | 29 | 0 | 7 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0001c0002t0009 | 0/0 | 6130 | 4 | 0 | 0 | 4 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6125): Show |
chr17 | 61860367 | 61932982 |
| a0001c0002t0011 | 0/0 | 6114 | 3 | 0 | 0 | 3 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6109): Show |
chr17 | 61860367 | 61932982 |
| a0001c0002t0027 | 0/0 | 6129 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0001c0002t0028 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6109): Show |
chr17 | 61860367 | 61932982 |
| a0001c0003t0002 | 0/0 | 6128 | 4 | 4 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0001c0004t0002 | 0/0 | 6128 | 2 | 0 | 0 | 2 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0002c0005t0001 | 0/0 | 6128 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0003c0009t0001 | 0/0 | 6128 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0004c0006t0024 | 0/0 | 6128 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0005c0007t0004 | 0/0 | 6129 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6124): Show |
chr17 | 61860367 | 61932982 |
| a0006c0010t0002 | 0/0 | 6128 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| a0007c0008t0023 | 0/1 | 6128 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | AGACC others(6123): Show |
chr17 | 61860367 | 61932982 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0007g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0007g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0007g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0008g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0008g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0008g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0008g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0010g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0012g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0013g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0013g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0014g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0014g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0016g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0017g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0018g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0019g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0020g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0021g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0022g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0025g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0001t0026g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0009g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0009g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0009g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0011g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0011g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0011g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0027g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0002t0028g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0003t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0003t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0003t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0004t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0001c0004t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0002c0005t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0003c0009t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0004c0006t0024g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0005c0007t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0006c0010t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| a0007c0008t0023g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0159 | EUR | GBR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00099 | hp2 | a0001 | c0001 | t0015 | g0001 | EUR | GBR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0162 | EUR | GBR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0087 | EUR | GBR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00423 | hp1 | a0001 | c0004 | t0002 | g0309 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00423 | hp2 | a0001 | c0002 | t0004 | g0075 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00438 | hp2 | a0001 | c0002 | t0004 | g0045 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0344 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0356 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0311 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0337 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00642 | hp1 | a0001 | c0002 | t0004 | g0042 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | CHS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01081 | hp2 | a0001 | c0002 | t0004 | g0061 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01099 | hp2 | a0001 | c0001 | t0026 | g0349 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0352 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0227 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0054 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01175 | hp1 | a0001 | c0002 | t0004 | g0066 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0354 | AMR | PUR | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01257 | hp2 | a0002 | c0005 | t0001 | g0086 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01346 | hp1 | a0001 | c0001 | t0018 | g0136 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0041 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0342 | AMR | CLM | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | IBS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0330 | EUR | IBS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0343 | EUR | IBS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0197 | EUR | IBS | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0248 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01928 | hp2 | a0001 | c0001 | t0025 | g0326 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0358 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0333 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0168 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02027 | hp1 | a0001 | c0001 | t0020 | g0245 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02055 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02055 | hp2 | a0001 | c0001 | t0013 | g0008 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02056 | hp1 | a0001 | c0002 | t0004 | g0078 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02071 | hp1 | a0001 | c0002 | t0028 | g0366 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02080 | hp1 | a0001 | c0002 | t0011 | g0363 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02132 | hp2 | a0001 | c0001 | t0021 | g0128 | EAS | KHV | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | CDX | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | CDX | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0015 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0073 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0056 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0347 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0091 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0335 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0359 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02735 | hp1 | a0001 | c0002 | t0027 | g0362 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0250 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02738 | hp2 | a0001 | c0001 | t0012 | g0205 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0216 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0328 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0057 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0350 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0351 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0346 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03486 | hp2 | a0001 | c0001 | t0022 | g0178 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0052 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0338 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03492 | hp2 | a0001 | c0001 | t0008 | g0339 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03540 | hp1 | a0001 | c0001 | t0016 | g0242 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | GWD | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0357 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | MSL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03710 | hp1 | a0001 | c0002 | t0004 | g0080 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0340 | SAS | PJL | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03831 | hp1 | a0001 | c0001 | t0008 | g0336 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0071 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03834 | hp2 | a0003 | c0009 | t0001 | g0140 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04184 | hp1 | a0001 | c0002 | t0004 | g0068 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04184 | hp2 | a0001 | c0001 | t0012 | g0207 | SAS | BEB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0226 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04199 | hp2 | a0001 | c0002 | t0004 | g0069 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG04228 | hp2 | a0001 | c0002 | t0004 | g0053 | SAS | STU | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0089 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18612 | hp1 | a0001 | c0001 | t0019 | g0104 | EAS | CHB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | CHB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18747 | hp1 | a0001 | c0002 | t0004 | g0043 | EAS | CHB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | CHB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18940 | hp1 | a0001 | c0002 | t0011 | g0364 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18941 | hp2 | a0004 | c0006 | t0024 | g0282 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18943 | hp2 | a0001 | c0002 | t0004 | g0361 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0050 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18948 | hp1 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18949 | hp1 | a0001 | c0001 | t0006 | g0196 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18950 | hp2 | a0001 | c0002 | t0004 | g0082 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18952 | hp1 | a0001 | c0002 | t0004 | g0055 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18956 | hp2 | a0001 | c0001 | t0017 | g0268 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18962 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18963 | hp1 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0319 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18965 | hp1 | a0001 | c0002 | t0004 | g0047 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18966 | hp2 | a0001 | c0002 | t0004 | g0058 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18967 | hp1 | a0001 | c0004 | t0002 | g0308 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18967 | hp2 | a0001 | c0002 | t0004 | g0079 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18968 | hp2 | a0005 | c0007 | t0004 | g0067 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18970 | hp1 | a0001 | c0002 | t0004 | g0059 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18972 | hp1 | a0001 | c0002 | t0004 | g0076 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18982 | hp2 | a0001 | c0002 | t0004 | g0072 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18985 | hp1 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18993 | hp2 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19007 | hp1 | a0001 | c0002 | t0004 | g0081 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0269 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19010 | hp1 | a0001 | c0002 | t0011 | g0365 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19010 | hp2 | a0001 | c0002 | t0009 | g0062 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19012 | hp1 | a0001 | c0002 | t0009 | g0046 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19030 | hp1 | a0001 | c0001 | t0013 | g0005 | AFR | LWK | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | LWK | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19054 | hp1 | a0001 | c0002 | t0009 | g0065 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19056 | hp2 | a0001 | c0002 | t0004 | g0280 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19058 | hp2 | a0001 | c0002 | t0009 | g0048 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19060 | hp2 | a0001 | c0002 | t0004 | g0084 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0355 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19074 | hp2 | a0001 | c0002 | t0004 | g0060 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19077 | hp2 | a0001 | c0002 | t0004 | g0085 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19079 | hp2 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19081 | hp2 | a0001 | c0002 | t0004 | g0049 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19082 | hp1 | a0001 | c0001 | t0006 | g0107 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19082 | hp2 | a0001 | c0002 | t0004 | g0074 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19084 | hp1 | a0001 | c0002 | t0004 | g0070 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19085 | hp2 | a0001 | c0002 | t0004 | g0083 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19090 | hp2 | a0006 | c0010 | t0002 | g0038 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19091 | hp2 | a0001 | c0002 | t0004 | g0064 | EAS | JPT | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0014 | AFR | YRI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0345 | AFR | ASW | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ASW | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0238 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02486 | hp1 | a0001 | c0001 | t0014 | g0144 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | USA | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | USA | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | USA | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0360 | AFR | LWK | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| NA21309 | hp2 | a0001 | c0003 | t0002 | g0013 | AFR | LWK | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| homoSapiens | chm13v2 | a0007 | c0008 | t0023 | g0131 | REF | REF | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0152 | REF | REF | INTS2_chr17_61860367_61932982 | INTS2 | chr17 | 61860367 | 61932982 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:61881042 | T | A | 1 | a0003 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.2219A>T | p.Asn740Ile | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/25 | 2566/6128 | 2219/3591 | 740/1196 | chr17 | 61881042 | |||
| chr17:61907425 | C | A | 1 | a0006 | 1 | NA19090.hp2 | missense_variant | MODERATE | c.1164G>T | p.Met388Ile | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/25 | 1511/6128 | 1164/3591 | 388/1196 | chr17 | 61907425 | |||
| chr17:61907499 | A | G | 1 | a0005 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1090T>C | p.Ser364Pro | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/25 | 1437/6128 | 1090/3591 | 364/1196 | chr17 | 61907499 | |||
| chr17:61907627 | C | T | 1 | a0004 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.962G>A | p.Arg321Lys | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/25 | 1309/6128 | 962/3591 | 321/1196 | chr17 | 61907627 | |||
| chr17:61925044 | C | T | 1 | a0002 | 1 | HG01257.hp2 | missense_variant | MODERATE | c.349G>A | p.Gly117Arg | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/25 | 696/6128 | 349/3591 | 117/1196 | chr17 | 61925044 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:61877919 | T | C | 1 | a0001c0003 | 4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
synonymous_variant | LOW | c.2424A>G | p.Leu808Leu | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/25 | 2771/6128 | 2424/3591 | 808/1196 | chr17 | 61877919 | |||
| chr17:61877952 | A | T | 1 | a0001c0004 | 2 | HG00423.hp1 NA18967.hp1 |
synonymous_variant | LOW | c.2391T>A | p.Val797Val | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/25 | 2738/6128 | 2391/3591 | 797/1196 | chr17 | 61877952 | |||
| chr17:61891639 | T | C | 2 | a0001c0002 a0005c0007 |
52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
synonymous_variant | LOW | c.1749A>G | p.Gln583Gln | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/25 | 2096/6128 | 1749/3591 | 583/1196 | chr17 | 61891639 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:61865470 | C | T | 1 | a0001c0001t0025 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2087G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 2087 | chr17 | 61865470 | ||||||
| chr17:61865553 | G | C | 1 | a0001c0001t0021 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2004C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 2004 | chr17 | 61865553 | ||||||
| chr17:61865707 | T | TA | 10 | a0001c0001t0004 a0001c0001t0019 a0001c0001t0020 others(7): Show |
56 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1849dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1849 | chr17 | 61865707 | ||||||
| chr17:61865927 | C | T | 2 | a0001c0001t0005 a0001c0001t0013 |
9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1630G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1630 | chr17 | 61865927 | ||||||
| chr17:61865973 | G | A | 2 | a0001c0001t0020 a0001c0001t0021 |
2 | HG02027.hp1 HG02132.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1584C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1584 | chr17 | 61865973 | ||||||
| chr17:61866060 | T | A | 1 | a0001c0001t0026 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1497A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1497 | chr17 | 61866060 | ||||||
| chr17:61866092 | C | T | 1 | a0001c0001t0022 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1465 | chr17 | 61866092 | ||||||
| chr17:61866171 | T | C | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
3_prime_UTR_variant | MODIFIER | c.*1386A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1386 | chr17 | 61866171 | ||||||
| chr17:61866343 | G | C | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(7): Show |
109 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*1214C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1214 | chr17 | 61866343 | ||||||
| chr17:61866346 | G | A | 1 | a0001c0001t0012 | 2 | HG02738.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1211C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1211 | chr17 | 61866346 | ||||||
| chr17:61866359 | G | GA | 5 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0010 others(2): Show |
19 | HG00621.hp1 HG02055.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1197dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1197 | chr17 | 61866359 | ||||||
| chr17:61866375 | A | C | 1 | a0001c0001t0018 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1182T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1182 | chr17 | 61866375 | ||||||
| chr17:61866404 | G | A | 1 | a0001c0002t0028 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1153C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1153 | chr17 | 61866404 | ||||||
| chr17:61866451 | A | T | 1 | a0001c0001t0008 | 4 | HG03491.hp1 HG03492.hp2 HG03710.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1106T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 1106 | chr17 | 61866451 | ||||||
| chr17:61866920 | A | C | 1 | a0001c0001t0017 | 1 | NA18956.hp2 | 3_prime_UTR_variant | MODIFIER | c.*637T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 637 | chr17 | 61866920 | ||||||
| chr17:61867050 | G | A | 1 | a0001c0001t0014 | 2 | HG02486.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*507C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 507 | chr17 | 61867050 | ||||||
| chr17:61867108 | C | T | 1 | a0001c0001t0016 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*449G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 25/25 | 449 | chr17 | 61867108 | ||||||
| chr17:61927824 | G | C | 1 | a0001c0002t0027 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-189C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/25 | 1180 | chr17 | 61927824 | ||||||
| chr17:61927878 | AGAACCGG others(8): Show |
A | 2 | a0001c0002t0011 a0001c0002t0028 |
4 | HG02071.hp1 HG02080.hp1 NA18940.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-258_-244delCTACAG others(9): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/25 | 1235 | chr17 | 61927878 | ||||||
| chr17:61927920 | A | G | 1 | a0001c0001t0015 | 1 | HG00099.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-285T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/25 | chr17 | 61927920 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:61867817 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3421+16T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 24/24 | chr17 | 61867817 | |||||||
| chr17:61868111 | A | C | 7 | a0001c0001t0003g0164 a0001c0001t0003g0170 a0001c0001t0003g0172 others(4): Show |
7 | NA18951.hp1 NA18961.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.3245-102T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868111 | |||||||
| chr17:61868207 | A | G | 34 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(31): Show |
34 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.3245-198T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868207 | |||||||
| chr17:61868465 | T | C | 2 | a0001c0001t0003g0176 a0001c0001t0003g0237 |
2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3245-456A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868465 | |||||||
| chr17:61868863 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3244+171C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868863 | |||||||
| chr17:61868889 | G | A | 4 | a0001c0002t0009g0062 a0001c0002t0011g0363 a0001c0002t0011g0364 others(1): Show |
4 | HG02071.hp1 HG02080.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.3244+145C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868889 | |||||||
| chr17:61868997 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3244+37A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 23/24 | chr17 | 61868997 | |||||||
| chr17:61869643 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3030+94A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 21/24 | chr17 | 61869643 | |||||||
| chr17:61870055 | A | C | 1 | a0001c0001t0002g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2779-67T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870055 | |||||||
| chr17:61870176 | T | G | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2779-188A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870176 | |||||||
| chr17:61870264 | A | C | 2 | a0001c0001t0003g0223 a0001c0001t0015g0001 |
2 | HG00099.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2779-276T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870264 | |||||||
| chr17:61870503 | C | T | 1 | a0001c0001t0002g0265 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2779-515G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870503 | |||||||
| chr17:61870669 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2779-681A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870669 | |||||||
| chr17:61870792 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2779-804C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61870792 | |||||||
| chr17:61871282 | G | A | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2778+983C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871282 | |||||||
| chr17:61871392 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2778+873C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871392 | |||||||
| chr17:61871427 | A | C | 1 | a0001c0003t0002g0013 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2778+838T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871427 | |||||||
| chr17:61871655 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2778+610G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871655 | |||||||
| chr17:61871814 | G | A | 2 | a0001c0001t0005g0006 a0001c0001t0005g0010 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2778+451C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871814 | |||||||
| chr17:61871940 | C | CAA | 9 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2778+323_2778+324d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61871940 | |||||||
| chr17:61872126 | T | A | 45 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.2778+139A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61872126 | |||||||
| chr17:61872168 | T | C | 1 | a0001c0001t0003g0232 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2778+97A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 20/24 | chr17 | 61872168 | |||||||
| chr17:61872689 | A | T | 1 | a0001c0001t0002g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2583-229T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61872689 | |||||||
| chr17:61872730 | C | T | 2 | a0001c0001t0002g0267 a0001c0001t0002g0313 |
2 | NA18940.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2583-270G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61872730 | |||||||
| chr17:61872775 | A | G | 5 | a0001c0001t0007g0002 a0001c0003t0002g0012 a0001c0003t0002g0013 others(2): Show |
5 | HG02257.hp2 HG03540.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.2583-315T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61872775 | |||||||
| chr17:61873014 | T | C | 1 | a0001c0001t0014g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2583-554A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873014 | |||||||
| chr17:61873142 | T | C | 103 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(100): Show |
103 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.2583-682A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873142 | |||||||
| chr17:61873231 | A | G | 1 | a0001c0001t0003g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2583-771T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873231 | |||||||
| chr17:61873293 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0191 |
2 | HG01261.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2583-833C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873293 | |||||||
| chr17:61873367 | A | T | 2 | a0001c0001t0003g0179 a0001c0001t0003g0180 |
2 | HG02300.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2583-907T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873367 | |||||||
| chr17:61873419 | A | C | 1 | a0001c0001t0002g0337 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2583-959T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873419 | |||||||
| chr17:61873693 | T | C | 2 | a0001c0001t0003g0181 a0001c0001t0003g0182 |
2 | HG01109.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2582+1220A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61873693 | |||||||
| chr17:61874079 | C | T | 2 | a0001c0001t0003g0181 a0001c0001t0003g0182 |
2 | HG01109.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2582+834G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874079 | |||||||
| chr17:61874104 | T | C | 1 | a0001c0002t0011g0365 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2582+809A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874104 | |||||||
| chr17:61874121 | C | G | 1 | a0001c0001t0003g0225 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2582+792G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874121 | |||||||
| chr17:61874202 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2582+711G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874202 | |||||||
| chr17:61874452 | G | C | 30 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(27): Show |
30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2582+461C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874452 | |||||||
| chr17:61874457 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2582+456G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874457 | |||||||
| chr17:61874640 | T | C | 1 | a0001c0001t0003g0168 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2582+273A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 19/24 | chr17 | 61874640 | |||||||
| chr17:61875326 | T | C | 8 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0003g0175 others(5): Show |
8 | HG02257.hp1 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2457-288A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875326 | |||||||
| chr17:61875379 | G | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0150 a0001c0001t0001g0219 |
3 | HG03130.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2457-341C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875379 | |||||||
| chr17:61875605 | A | C | 4 | a0001c0001t0003g0173 a0001c0001t0003g0174 a0001c0001t0003g0234 others(1): Show |
4 | HG02257.hp1 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2457-567T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875605 | |||||||
| chr17:61875673 | C | T | 2 | a0001c0001t0003g0181 a0001c0001t0003g0182 |
2 | HG01109.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.2457-635G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875673 | |||||||
| chr17:61875755 | G | A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2457-717C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875755 | |||||||
| chr17:61875891 | A | G | 30 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(27): Show |
30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2457-853T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875891 | |||||||
| chr17:61875953 | G | C | 12 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0005g0003 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2457-915C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61875953 | |||||||
| chr17:61876029 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2457-991C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876029 | |||||||
| chr17:61876129 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2457-1091G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876129 | |||||||
| chr17:61876462 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2457-1424C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876462 | |||||||
| chr17:61876529 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2456+1358G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876529 | |||||||
| chr17:61876545 | C | T | 11 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0101 others(8): Show |
11 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.2456+1342G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876545 | |||||||
| chr17:61876812 | G | A | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2456+1075C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61876812 | |||||||
| chr17:61877014 | T | C | 1 | a0001c0001t0002g0264 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2456+873A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61877014 | |||||||
| chr17:61877169 | T | C | 22 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 others(19): Show |
22 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.2456+718A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61877169 | |||||||
| chr17:61877221 | A | C | 1 | a0001c0001t0003g0229 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2456+666T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61877221 | |||||||
| chr17:61877349 | G | A | 1 | a0001c0002t0004g0056 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2456+538C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 18/24 | chr17 | 61877349 | |||||||
| chr17:61878526 | C | T | 45 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.2255-438G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878526 | |||||||
| chr17:61878637 | A | AT | 42 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
42 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.2255-550dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878637 | |||||||
| chr17:61878833 | G | C | 52 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(49): Show |
52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.2255-745C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878833 | |||||||
| chr17:61878854 | C | A | 1 | a0001c0001t0003g0169 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2255-766G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878854 | |||||||
| chr17:61878921 | A | G | 42 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
42 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.2255-833T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878921 | |||||||
| chr17:61878931 | C | CA | 80 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(77): Show |
80 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2255-844dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878931 | |||||||
| chr17:61878931 | C | CAA | 100 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0098 others(97): Show |
100 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(97): Show |
intron_variant | MODIFIER | c.2255-845_2255-844d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878931 | |||||||
| chr17:61878931 | C | CAAA | 73 | a0001c0001t0001g0100 a0001c0001t0001g0188 a0001c0001t0001g0189 others(70): Show |
73 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.2255-846_2255-844d others(5): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878931 | |||||||
| chr17:61878931 | C | CAAAA | 26 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0145 others(23): Show |
26 | HG00140.hp2 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2255-847_2255-844d others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878931 | |||||||
| chr17:61878944 | A | AAAAAAAA others(3): Show |
10 | a0001c0001t0003g0021 a0001c0001t0003g0023 a0001c0001t0003g0025 others(7): Show |
10 | HG01891.hp1 HG02257.hp1 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.2255-857_2255-856i others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878944 | |||||||
| chr17:61878944 | A | AAAAAAAA others(2): Show |
23 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(20): Show |
23 | HG00639.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.2255-857_2255-856i others(11): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878944 | |||||||
| chr17:61878944 | A | AAAAAAAA others(1): Show |
8 | a0001c0001t0003g0243 a0001c0001t0005g0003 a0001c0001t0005g0004 others(5): Show |
8 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2255-857_2255-856i others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878944 | |||||||
| chr17:61878944 | A | C | 1 | a0001c0001t0003g0234 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2255-856T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61878944 | |||||||
| chr17:61879071 | C | CT | 49 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0099 others(46): Show |
49 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.2255-984dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | |||||||
| chr17:61879071 | C | CTT | 8 | a0001c0001t0001g0153 a0001c0001t0002g0314 a0001c0001t0002g0333 others(5): Show |
8 | HG00140.hp2 HG01099.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.2255-985_2255-984d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | |||||||
| chr17:61879071 | CT | C | 134 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0145 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2255-984delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | |||||||
| chr17:61879071 | CTT | C | 16 | a0001c0001t0002g0328 a0001c0001t0002g0334 a0001c0001t0002g0346 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2255-985_2255-984d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | |||||||
| chr17:61879071 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2255-995_2255-984d others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | |||||||
| chr17:61879071 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2255-998_2255-984d others(17): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879071 | |||||||
| chr17:61879200 | G | C | 13 | a0001c0001t0003g0151 a0001c0001t0003g0155 a0001c0001t0003g0156 others(10): Show |
13 | HG01074.hp2 HG01106.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.2255-1112C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879200 | |||||||
| chr17:61879457 | A | G | 1 | a0001c0001t0002g0335 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2255-1369T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879457 | |||||||
| chr17:61879875 | T | G | 1 | a0001c0002t0004g0047 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2254+1132A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879875 | |||||||
| chr17:61879887 | A | C | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2254+1120T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61879887 | |||||||
| chr17:61880075 | G | A | 1 | a0001c0001t0003g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2254+932C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880075 | |||||||
| chr17:61880169 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2254+838C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880169 | |||||||
| chr17:61880239 | G | A | 2 | a0001c0001t0002g0262 a0001c0001t0002g0264 |
2 | HG00673.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2254+768C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880239 | |||||||
| chr17:61880261 | T | C | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2254+746A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880261 | |||||||
| chr17:61880709 | G | A | 1 | a0001c0002t0004g0056 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2254+298C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880709 | |||||||
| chr17:61880787 | G | C | 95 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(92): Show |
95 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2254+220C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880787 | |||||||
| chr17:61880819 | A | G | 1 | a0001c0001t0022g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2254+188T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880819 | |||||||
| chr17:61880902 | T | C | 111 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0145 others(108): Show |
111 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.2254+105A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880902 | |||||||
| chr17:61880929 | T | C | 9 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2254+78A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 17/24 | chr17 | 61880929 | |||||||
| chr17:61881274 | G | T | 115 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0145 others(112): Show |
115 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.2090-103C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61881274 | |||||||
| chr17:61881351 | C | A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2090-180G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61881351 | |||||||
| chr17:61881426 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0222 |
2 | HG03490.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.2090-255C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61881426 | |||||||
| chr17:61882185 | A | C | 45 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.2090-1014T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882185 | |||||||
| chr17:61882228 | C | T | 109 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(106): Show |
109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.2090-1057G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882228 | |||||||
| chr17:61882404 | G | C | 81 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(78): Show |
81 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.2090-1233C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882404 | |||||||
| chr17:61882500 | A | G | 2 | a0001c0001t0002g0344 a0001c0001t0002g0353 |
2 | HG00438.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.2090-1329T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882500 | |||||||
| chr17:61882601 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2090-1430G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882601 | |||||||
| chr17:61882741 | G | A | 1 | a0001c0001t0002g0265 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2090-1570C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882741 | |||||||
| chr17:61882809 | A | C | 1 | a0001c0001t0016g0242 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2090-1638T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61882809 | |||||||
| chr17:61883056 | C | T | 250 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.2089+1845G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883056 | |||||||
| chr17:61883311 | G | C | 16 | a0001c0001t0002g0095 a0001c0001t0002g0184 a0001c0001t0002g0265 others(13): Show |
16 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.2089+1590C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883311 | |||||||
| chr17:61883343 | T | A | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2089+1558A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883343 | |||||||
| chr17:61883378 | C | T | 363 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0096 others(360): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.2089+1523G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883378 | |||||||
| chr17:61883390 | C | A | 363 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0096 others(360): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.2089+1511G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883390 | |||||||
| chr17:61883406 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0135 a0001c0001t0003g0091 |
3 | HG01358.hp2 HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2089+1495C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883406 | |||||||
| chr17:61883523 | G | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0214 a0001c0001t0001g0221 others(1): Show |
4 | HG02896.hp2 HG02897.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.2089+1378C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883523 | |||||||
| chr17:61883604 | T | C | 2 | a0001c0001t0003g0157 a0001c0001t0003g0160 |
2 | HG00408.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2089+1297A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61883604 | |||||||
| chr17:61884001 | G | GA | 51 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(48): Show |
51 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.2089+899dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884001 | |||||||
| chr17:61884001 | GA | G | 48 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(45): Show |
48 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.2089+899delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884001 | |||||||
| chr17:61884152 | T | C | 30 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(27): Show |
30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2089+749A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884152 | |||||||
| chr17:61884554 | A | T | 1 | a0001c0001t0003g0358 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2089+347T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884554 | |||||||
| chr17:61884555 | A | T | 95 | a0001c0001t0001g0097 a0001c0001t0001g0256 a0001c0001t0001g0259 others(92): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(92): Show |
intron_variant | MODIFIER | c.2089+346T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884555 | |||||||
| chr17:61884556 | T | A | 18 | a0001c0001t0001g0212 a0001c0001t0002g0274 a0001c0001t0003g0016 others(15): Show |
18 | HG00639.hp1 HG00642.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.2089+345A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 16/24 | chr17 | 61884556 | |||||||
| chr17:61885113 | A | G | 1 | a0001c0002t0004g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1985-108T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885113 | |||||||
| chr17:61885155 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1985-150G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885155 | |||||||
| chr17:61885223 | T | C | 42 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
42 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1985-218A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885223 | |||||||
| chr17:61885359 | T | C | 250 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1985-354A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885359 | |||||||
| chr17:61885360 | G | T | 1 | a0001c0001t0002g0350 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1985-355C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885360 | |||||||
| chr17:61885414 | C | CT | 42 | a0001c0001t0001g0111 a0001c0001t0001g0188 a0001c0001t0001g0213 others(39): Show |
42 | HG00639.hp1 HG00733.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.1985-410dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885414 | |||||||
| chr17:61885414 | CT | C | 94 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(91): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(91): Show |
intron_variant | MODIFIER | c.1985-410delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885414 | |||||||
| chr17:61885428 | T | C | 110 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(107): Show |
110 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1985-423A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885428 | |||||||
| chr17:61885603 | A | G | 42 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
42 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1985-598T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885603 | |||||||
| chr17:61885714 | G | A | 1 | a0001c0001t0020g0245 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1985-709C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885714 | |||||||
| chr17:61885721 | C | A | 3 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1985-716G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885721 | |||||||
| chr17:61885723 | A | AT | 44 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0111 others(41): Show |
44 | HG00642.hp1 HG01109.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.1985-719dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885723 | |||||||
| chr17:61885723 | AT | A | 134 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(131): Show |
134 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.1985-719delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885723 | |||||||
| chr17:61885761 | G | A | 1 | a0001c0001t0003g0155 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1985-756C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885761 | |||||||
| chr17:61885950 | G | A | 1 | a0001c0001t0003g0025 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1985-945C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61885950 | |||||||
| chr17:61886192 | A | T | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1985-1187T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886192 | |||||||
| chr17:61886251 | A | G | 51 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(48): Show |
51 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1985-1246T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886251 | |||||||
| chr17:61886356 | G | A | 109 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(106): Show |
109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1985-1351C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886356 | |||||||
| chr17:61886418 | A | C | 152 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(149): Show |
152 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.1985-1413T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886418 | |||||||
| chr17:61886550 | C | T | 105 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(102): Show |
105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1985-1545G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886550 | |||||||
| chr17:61886553 | C | A | 22 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(19): Show |
22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1985-1548G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886553 | |||||||
| chr17:61886658 | A | C | 1 | a0001c0001t0026g0349 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1985-1653T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886658 | |||||||
| chr17:61886733 | G | A | 22 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(19): Show |
22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1985-1728C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61886733 | |||||||
| chr17:61887065 | C | T | 1 | a0001c0002t0004g0045 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1985-2060G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887065 | |||||||
| chr17:61887183 | A | T | 3 | a0001c0003t0002g0012 a0001c0003t0002g0014 a0001c0003t0002g0015 |
3 | HG02257.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1985-2178T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887183 | |||||||
| chr17:61887338 | T | C | 145 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(142): Show |
145 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.1985-2333A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887338 | |||||||
| chr17:61887405 | C | G | 1 | a0001c0001t0003g0249 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1984+2381G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887405 | |||||||
| chr17:61887438 | G | A | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1984+2348C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887438 | |||||||
| chr17:61887458 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1984+2328C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887458 | |||||||
| chr17:61887466 | C | G | 1 | a0001c0001t0002g0297 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1984+2320G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887466 | |||||||
| chr17:61887482 | C | CA | 27 | a0001c0001t0001g0100 a0001c0001t0001g0133 a0001c0001t0001g0241 others(24): Show |
27 | HG00140.hp2 HG00597.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1984+2303dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887482 | |||||||
| chr17:61887482 | CA | C | 6 | a0001c0001t0001g0126 a0001c0001t0001g0143 a0001c0001t0001g0211 others(3): Show |
6 | HG01243.hp1 HG01255.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1984+2303delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887482 | |||||||
| chr17:61887722 | A | G | 7 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1984+2064T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887722 | |||||||
| chr17:61887746 | G | C | 2 | a0001c0001t0005g0006 a0001c0001t0005g0010 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1984+2040C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887746 | |||||||
| chr17:61887775 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1984+2011C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887775 | |||||||
| chr17:61887790 | C | T | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1984+1996G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887790 | |||||||
| chr17:61887815 | G | A | 4 | a0001c0001t0002g0329 a0001c0001t0002g0334 a0001c0001t0002g0346 others(1): Show |
4 | HG02717.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1984+1971C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61887815 | |||||||
| chr17:61888235 | T | C | 6 | a0001c0001t0001g0102 a0001c0001t0001g0119 a0001c0001t0001g0121 others(3): Show |
6 | HG00280.hp2 HG01071.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.1984+1551A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888235 | |||||||
| chr17:61888389 | A | G | 1 | a0001c0001t0002g0266 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1984+1397T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888389 | |||||||
| chr17:61888556 | T | TGTGC | 8 | a0001c0001t0002g0288 a0001c0001t0002g0329 a0001c0001t0002g0334 others(5): Show |
8 | HG01109.hp2 HG02717.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.1984+1226_1984+122 others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888556 | |||||||
| chr17:61888556 | T | TGTGCGTG others(5): Show |
1 | a0001c0001t0003g0179 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1984+1229_1984+123 others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888556 | |||||||
| chr17:61888564 | C | CGT | 3 | a0001c0001t0001g0112 a0001c0001t0001g0147 a0001c0001t0006g0210 |
3 | HG01168.hp2 NA18959.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1984+1220_1984+122 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | |||||||
| chr17:61888564 | C | CGTGCGTG others(5): Show |
25 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(22): Show |
25 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1984+1221_1984+122 others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | |||||||
| chr17:61888564 | C | CGTGCGTG others(7): Show |
1 | a0001c0001t0003g0176 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1984+1221_1984+122 others(18): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | |||||||
| chr17:61888564 | C | CGTGCGTG others(9): Show |
1 | a0001c0001t0003g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1984+1221_1984+122 others(20): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | |||||||
| chr17:61888564 | C | CGTGCGTG others(3): Show |
2 | a0001c0001t0003g0025 a0001c0001t0003g0091 |
2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1984+1221_1984+122 others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | |||||||
| chr17:61888564 | CGT | C | 5 | a0001c0001t0001g0139 a0001c0001t0003g0032 a0001c0001t0003g0230 others(2): Show |
5 | HG02698.hp2 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1984+1220_1984+122 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888564 | |||||||
| chr17:61888566 | T | TGC | 141 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(138): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.1984+1219_1984+122 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888566 | |||||||
| chr17:61888566 | T | TGCGTGC | 12 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0005g0003 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1984+1219_1984+122 others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888566 | |||||||
| chr17:61888568 | T | C | 63 | a0001c0001t0001g0141 a0001c0001t0002g0288 a0001c0001t0002g0329 others(60): Show |
63 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1984+1218A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888568 | |||||||
| chr17:61888570 | T | C | 102 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(99): Show |
102 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1984+1216A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888570 | |||||||
| chr17:61888572 | T | C | 2 | a0001c0001t0002g0345 a0001c0001t0002g0354 |
2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1984+1214A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888572 | |||||||
| chr17:61888574 | T | C | 1 | a0001c0001t0022g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1984+1212A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888574 | |||||||
| chr17:61888681 | T | C | 1 | a0001c0001t0002g0327 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1984+1105A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888681 | |||||||
| chr17:61888790 | C | T | 1 | a0001c0002t0004g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1984+996G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888790 | |||||||
| chr17:61888810 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1984+976C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61888810 | |||||||
| chr17:61889020 | C | CAAAAACA | 22 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(19): Show |
22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1984+759_1984+765d others(9): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889020 | |||||||
| chr17:61889020 | C | CAAAAACA others(7): Show |
9 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1984+752_1984+765d others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889020 | |||||||
| chr17:61889020 | CAAAAACA | C | 51 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(48): Show |
51 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1984+759_1984+765d others(9): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889020 | |||||||
| chr17:61889020 | CAAAAACA others(7): Show |
C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1984+752_1984+765d others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889020 | |||||||
| chr17:61889067 | A | C | 12 | a0001c0001t0002g0095 a0001c0001t0002g0265 a0001c0001t0002g0270 others(9): Show |
12 | HG00423.hp1 HG00621.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.1984+719T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889067 | |||||||
| chr17:61889069 | C | A | 108 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(105): Show |
108 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1984+717G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889069 | |||||||
| chr17:61889091 | C | CT | 109 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(106): Show |
109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1984+694dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889091 | |||||||
| chr17:61889275 | CG | C | 51 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(48): Show |
51 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1984+510delC | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889275 | |||||||
| chr17:61889380 | A | T | 241 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1984+406T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889380 | |||||||
| chr17:61889443 | T | G | 42 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(39): Show |
42 | HG00639.hp1 HG01891.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.1984+343A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889443 | |||||||
| chr17:61889483 | C | T | 1 | a0001c0001t0003g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1984+303G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889483 | |||||||
| chr17:61889625 | G | T | 1 | a0001c0001t0018g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1984+161C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 15/24 | chr17 | 61889625 | |||||||
| chr17:61889901 | G | T | 1 | a0001c0001t0003g0088 | 1 | HG02717.hp2 | splice_region_variant&intron_variant | LOW | c.1876-7C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61889901 | |||||||
| chr17:61889929 | T | C | 8 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0332 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1876-35A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61889929 | |||||||
| chr17:61890026 | T | C | 105 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(102): Show |
105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1876-132A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890026 | |||||||
| chr17:61890033 | G | A | 7 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1876-139C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890033 | |||||||
| chr17:61890312 | C | T | 1 | a0001c0002t0011g0363 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1876-418G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890312 | |||||||
| chr17:61890343 | G | A | 1 | a0001c0002t0011g0363 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1876-449C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890343 | |||||||
| chr17:61890418 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1876-524A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890418 | |||||||
| chr17:61890441 | C | A | 1 | a0001c0001t0002g0337 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1876-547G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890441 | |||||||
| chr17:61890490 | A | T | 1 | a0001c0002t0004g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1876-596T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890490 | |||||||
| chr17:61890491 | T | C | 1 | a0001c0002t0004g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1876-597A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890491 | |||||||
| chr17:61890494 | C | T | 1 | a0001c0002t0004g0076 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1876-600G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890494 | |||||||
| chr17:61890513 | G | A | 1 | a0001c0002t0004g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1876-619C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890513 | |||||||
| chr17:61890579 | C | T | 97 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(94): Show |
97 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(94): Show |
intron_variant | MODIFIER | c.1876-685G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890579 | |||||||
| chr17:61890609 | C | CA | 90 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0105 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1876-716dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890609 | |||||||
| chr17:61890609 | C | CAA | 16 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0158 others(13): Show |
16 | HG01978.hp1 HG02055.hp2 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1876-717_1876-716d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890609 | |||||||
| chr17:61890609 | CA | C | 128 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(125): Show |
128 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1876-716delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890609 | |||||||
| chr17:61890756 | T | A | 22 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(19): Show |
22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1875+757A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890756 | |||||||
| chr17:61890789 | C | T | 1 | a0001c0003t0002g0013 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1875+724G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890789 | |||||||
| chr17:61890864 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1875+649C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890864 | |||||||
| chr17:61890961 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1875+552A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890961 | |||||||
| chr17:61890983 | C | CA | 164 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0097 others(161): Show |
164 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1875+529dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890983 | |||||||
| chr17:61890983 | CA | C | 30 | a0001c0001t0002g0034 a0001c0001t0002g0095 a0001c0001t0002g0261 others(27): Show |
30 | HG01099.hp2 HG01515.hp2 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.1875+529delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890983 | |||||||
| chr17:61890983 | CAAAAAAA others(8): Show |
C | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1875+515_1875+529d others(17): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61890983 | |||||||
| chr17:61891012 | G | A | 2 | a0001c0001t0002g0296 a0001c0001t0007g0002 |
2 | HG03579.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1875+501C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891012 | |||||||
| chr17:61891091 | C | T | 52 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(49): Show |
52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1875+422G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891091 | |||||||
| chr17:61891190 | G | A | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1875+323C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891190 | |||||||
| chr17:61891210 | A | C | 64 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0005g0003 others(61): Show |
64 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1875+303T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891210 | |||||||
| chr17:61891219 | C | T | 2 | a0001c0001t0005g0006 a0001c0001t0005g0010 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1875+294G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891219 | |||||||
| chr17:61891249 | T | A | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1875+264A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891249 | |||||||
| chr17:61891260 | T | C | 151 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(148): Show |
151 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.1875+253A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891260 | |||||||
| chr17:61891464 | G | A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1875+49C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 14/24 | chr17 | 61891464 | |||||||
| chr17:61891871 | A | T | 143 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(140): Show |
143 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1699-182T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61891871 | |||||||
| chr17:61891920 | C | A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1699-231G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61891920 | |||||||
| chr17:61891924 | T | TTAATCTA others(321): Show |
1 | a0005c0007t0004g0067 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1699-236_1699-235i others(330): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61891924 | |||||||
| chr17:61892019 | G | A | 3 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1699-330C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892019 | |||||||
| chr17:61892172 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1699-483G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892172 | |||||||
| chr17:61892397 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1699-708G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892397 | |||||||
| chr17:61892444 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1699-755C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892444 | |||||||
| chr17:61892557 | C | T | 2 | a0001c0001t0003g0179 a0001c0001t0003g0180 |
2 | HG02300.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1699-868G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892557 | |||||||
| chr17:61892562 | T | C | 6 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | NA18612.hp1 NA18946.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.1699-873A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892562 | |||||||
| chr17:61892583 | G | A | 14 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0243 others(11): Show |
14 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1699-894C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892583 | |||||||
| chr17:61892586 | G | T | 2 | a0001c0001t0003g0019 a0001c0001t0003g0027 |
2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1699-897C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892586 | |||||||
| chr17:61892590 | A | C | 1 | a0001c0001t0002g0348 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1699-901T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892590 | |||||||
| chr17:61892720 | G | A | 1 | a0001c0001t0003g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1699-1031C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892720 | |||||||
| chr17:61892789 | TA | T | 9 | a0001c0001t0001g0112 a0001c0001t0002g0266 a0001c0001t0002g0303 others(6): Show |
9 | HG01074.hp2 HG01515.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1698+975delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892789 | |||||||
| chr17:61892854 | G | A | 5 | a0001c0001t0003g0169 a0001c0003t0002g0012 a0001c0003t0002g0013 others(2): Show |
5 | HG01978.hp1 HG02257.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1698+911C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892854 | |||||||
| chr17:61892953 | C | CA | 17 | a0001c0001t0001g0094 a0001c0001t0001g0098 a0001c0001t0001g0110 others(14): Show |
17 | HG01167.hp1 HG02622.hp1 HG02738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1698+811dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892953 | |||||||
| chr17:61892953 | CA | C | 222 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(219): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1698+811delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892953 | |||||||
| chr17:61892953 | CAA | C | 8 | a0001c0001t0002g0303 a0001c0001t0002g0342 a0001c0001t0002g0343 others(5): Show |
8 | HG01074.hp2 HG01099.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1698+810_1698+811d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892953 | |||||||
| chr17:61892984 | G | A | 1 | a0001c0001t0003g0089 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1698+781C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892984 | |||||||
| chr17:61892991 | C | CT | 45 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.1698+773dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61892991 | |||||||
| chr17:61893004 | T | C | 30 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(27): Show |
30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1698+761A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893004 | |||||||
| chr17:61893148 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1698+617A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893148 | |||||||
| chr17:61893154 | A | G | 250 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(247): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1698+611T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893154 | |||||||
| chr17:61893236 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1698+529A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893236 | |||||||
| chr17:61893347 | G | A | 4 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0166 others(1): Show |
4 | HG02280.hp2 HG03490.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.1698+418C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893347 | |||||||
| chr17:61893347 | G | C | 7 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1698+418C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893347 | |||||||
| chr17:61893435 | C | T | 22 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(19): Show |
22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1698+330G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893435 | |||||||
| chr17:61893476 | A | G | 30 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(27): Show |
30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1698+289T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893476 | |||||||
| chr17:61893546 | T | C | 45 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.1698+219A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893546 | |||||||
| chr17:61893554 | G | A | 1 | a0001c0002t0004g0069 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1698+211C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893554 | |||||||
| chr17:61893691 | T | C | 3 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1698+74A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893691 | |||||||
| chr17:61893706 | A | T | 144 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0352 others(141): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1698+59T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 13/24 | chr17 | 61893706 | |||||||
| chr17:61894402 | T | C | 30 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(27): Show |
30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1564-503A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894402 | |||||||
| chr17:61894621 | G | A | 104 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(101): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1563+694C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894621 | |||||||
| chr17:61894773 | A | G | 2 | a0001c0001t0003g0032 a0001c0001t0003g0252 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1563+542T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894773 | |||||||
| chr17:61894810 | T | C | 108 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(105): Show |
108 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1563+505A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894810 | |||||||
| chr17:61894839 | T | TTA | 30 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(27): Show |
30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1563+475_1563+476i others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894839 | |||||||
| chr17:61894839 | TA | T | 161 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(158): Show |
161 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1563+475delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894839 | |||||||
| chr17:61894912 | T | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1563+403A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894912 | |||||||
| chr17:61894930 | T | C | 3 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1563+385A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61894930 | |||||||
| chr17:61895116 | C | G | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1563+199G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 12/24 | chr17 | 61895116 | |||||||
| chr17:61895516 | T | G | 1 | a0001c0001t0003g0230 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1495-133A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61895516 | |||||||
| chr17:61895718 | G | A | 242 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1495-335C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61895718 | |||||||
| chr17:61895891 | T | C | 3 | a0001c0001t0001g0102 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG01071.hp2 HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1495-508A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61895891 | |||||||
| chr17:61895894 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1495-511T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61895894 | |||||||
| chr17:61895998 | T | A | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(43): Show |
46 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1495-615A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61895998 | |||||||
| chr17:61896097 | G | A | 1 | a0001c0001t0002g0314 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1495-714C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896097 | |||||||
| chr17:61896100 | C | T | 7 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1495-717G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896100 | |||||||
| chr17:61896124 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1495-741G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896124 | |||||||
| chr17:61896171 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1495-788G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896171 | |||||||
| chr17:61896195 | G | A | 53 | a0001c0001t0006g0107 a0001c0002t0004g0039 a0001c0002t0004g0040 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1495-812C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896195 | |||||||
| chr17:61896239 | C | CA | 18 | a0001c0001t0001g0092 a0001c0001t0002g0275 a0001c0001t0002g0278 others(15): Show |
18 | HG00621.hp1 HG00621.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1495-857dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896239 | |||||||
| chr17:61896251 | AC | A | 43 | a0001c0001t0002g0341 a0001c0001t0003g0051 a0001c0001t0003g0052 others(40): Show |
43 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(40): Show |
intron_variant | MODIFIER | c.1495-869delG | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896251 | |||||||
| chr17:61896252 | C | A | 208 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(205): Show |
208 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.1495-869G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896252 | |||||||
| chr17:61896256 | A | C | 1 | a0001c0002t0004g0082 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1495-873T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896256 | |||||||
| chr17:61896260 | A | C | 1 | a0001c0001t0003g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1495-877T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896260 | |||||||
| chr17:61896471 | C | T | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1494+998G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896471 | |||||||
| chr17:61896805 | A | G | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+664T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896805 | |||||||
| chr17:61896856 | C | A | 45 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.1494+613G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896856 | |||||||
| chr17:61896933 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1494+536G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61896933 | |||||||
| chr17:61897027 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1494+442A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61897027 | |||||||
| chr17:61897290 | A | G | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(43): Show |
46 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1494+179T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61897290 | |||||||
| chr17:61897348 | T | G | 30 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(27): Show |
30 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1494+121A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 11/24 | chr17 | 61897348 | |||||||
| chr17:61897944 | C | T | 1 | a0001c0002t0009g0062 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1308-205G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61897944 | |||||||
| chr17:61898011 | T | C | 109 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(106): Show |
109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1308-272A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898011 | |||||||
| chr17:61898088 | T | C | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308-349A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898088 | |||||||
| chr17:61898093 | A | G | 2 | a0001c0001t0005g0007 a0001c0001t0005g0011 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1308-354T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898093 | |||||||
| chr17:61898406 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1308-667G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898406 | |||||||
| chr17:61898407 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1308-668T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898407 | |||||||
| chr17:61898408 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1308-669G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898408 | |||||||
| chr17:61898578 | G | A | 9 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1308-839C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898578 | |||||||
| chr17:61898602 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1308-863A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898602 | |||||||
| chr17:61898650 | G | A | 8 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0332 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1308-911C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898650 | |||||||
| chr17:61898675 | G | C | 4 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0013g0005 others(1): Show |
4 | HG02055.hp2 HG02818.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1308-936C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898675 | |||||||
| chr17:61898716 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1308-977G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898716 | |||||||
| chr17:61898739 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0148 a0001c0001t0001g0217 others(1): Show |
4 | HG01099.hp1 HG01243.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308-1000C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61898739 | |||||||
| chr17:61899166 | C | A | 3 | a0001c0001t0003g0175 a0001c0001t0003g0235 a0001c0001t0003g0236 |
3 | HG02809.hp1 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1308-1427G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899166 | |||||||
| chr17:61899179 | T | C | 8 | a0001c0001t0002g0261 a0001c0001t0002g0267 a0001c0001t0002g0273 others(5): Show |
8 | HG02129.hp1 HG02155.hp2 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1308-1440A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899179 | |||||||
| chr17:61899200 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1308-1461C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899200 | |||||||
| chr17:61899231 | A | T | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1308-1492T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899231 | |||||||
| chr17:61899416 | A | G | 9 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1308-1677T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899416 | |||||||
| chr17:61899482 | C | A | 3 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1308-1743G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899482 | |||||||
| chr17:61899606 | A | G | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1308-1867T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899606 | |||||||
| chr17:61899813 | A | G | 105 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(102): Show |
105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1308-2074T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899813 | |||||||
| chr17:61899839 | G | A | 1 | a0001c0002t0004g0058 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1308-2100C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899839 | |||||||
| chr17:61899908 | T | C | 1 | a0001c0001t0018g0136 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1308-2169A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899908 | |||||||
| chr17:61899910 | TA | T | 254 | a0001c0001t0001g0111 a0001c0001t0001g0123 a0001c0001t0001g0129 others(251): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1308-2172delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899910 | |||||||
| chr17:61899927 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1308-2188A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61899927 | |||||||
| chr17:61900205 | A | G | 3 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1308-2466T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900205 | |||||||
| chr17:61900323 | C | T | 1 | a0001c0002t0004g0054 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1308-2584G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900323 | |||||||
| chr17:61900434 | T | C | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308-2695A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900434 | |||||||
| chr17:61900673 | A | C | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308-2934T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900673 | |||||||
| chr17:61900702 | A | T | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1308-2963T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900702 | |||||||
| chr17:61900756 | G | A | 5 | a0001c0001t0002g0289 a0001c0001t0002g0303 a0001c0001t0002g0304 others(2): Show |
5 | HG01993.hp1 NA18945.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308-3017C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900756 | |||||||
| chr17:61900812 | G | C | 105 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(102): Show |
105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1308-3073C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900812 | |||||||
| chr17:61900851 | G | A | 3 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1308-3112C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61900851 | |||||||
| chr17:61901015 | C | T | 104 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(101): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1308-3276G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901015 | |||||||
| chr17:61901061 | G | C | 1 | a0001c0002t0004g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1308-3322C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901061 | |||||||
| chr17:61901204 | A | C | 1 | a0001c0001t0003g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1307+3256T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901204 | |||||||
| chr17:61901363 | G | T | 108 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(105): Show |
108 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.1307+3097C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901363 | |||||||
| chr17:61901435 | T | G | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1307+3025A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901435 | |||||||
| chr17:61901491 | G | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1307+2969C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901491 | |||||||
| chr17:61901577 | C | CT | 62 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0125 others(59): Show |
62 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1307+2882dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | C | CTT | 34 | a0001c0001t0001g0103 a0001c0001t0001g0240 a0001c0001t0001g0241 others(31): Show |
34 | HG00438.hp1 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1307+2881_1307+288 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | C | CTTT | 9 | a0001c0001t0002g0264 a0001c0001t0002g0327 a0001c0001t0002g0330 others(6): Show |
9 | HG01081.hp1 HG01243.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1307+2880_1307+288 others(7): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CT | C | 29 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(26): Show |
29 | HG01070.hp1 HG01255.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1307+2882delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTT | C | 11 | a0001c0001t0001g0097 a0001c0001t0003g0016 a0001c0001t0003g0023 others(8): Show |
11 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1307+2881_1307+288 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTT | C | 6 | a0001c0001t0003g0017 a0001c0001t0003g0019 a0001c0001t0003g0020 others(3): Show |
6 | HG02451.hp1 HG02896.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307+2880_1307+288 others(7): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTT | C | 7 | a0001c0001t0002g0033 a0001c0001t0002g0035 a0001c0001t0002g0037 others(4): Show |
7 | HG02257.hp2 NA18993.hp1 NA19074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1307+2877_1307+288 others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(1): Show |
C | 7 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 others(4): Show |
7 | HG02145.hp1 HG02717.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1307+2875_1307+288 others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(2): Show |
C | 35 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0151 others(32): Show |
35 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.1307+2874_1307+288 others(13): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0187 |
3 | HG00140.hp1 NA18942.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.1307+2873_1307+288 others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0254 |
2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1307+2872_1307+288 others(15): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(5): Show |
C | 54 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0096 others(51): Show |
54 | HG00280.hp2 HG00558.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.1307+2871_1307+288 others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0202 a0001c0001t0002g0262 others(1): Show |
4 | HG00673.hp2 HG01346.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307+2870_1307+288 others(17): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0002g0284 a0001c0001t0002g0285 |
2 | HG02040.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1307+2869_1307+288 others(18): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1307+2866_1307+288 others(21): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(11): Show |
C | 2 | a0001c0002t0004g0044 a0001c0002t0004g0053 |
2 | HG04228.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1307+2865_1307+288 others(22): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(12): Show |
C | 51 | a0001c0001t0001g0111 a0001c0001t0006g0107 a0001c0002t0004g0039 others(48): Show |
51 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.1307+2864_1307+288 others(23): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901577 | CTTTTTTT others(13): Show |
C | 2 | a0001c0001t0002g0263 a0001c0002t0004g0078 |
2 | HG02056.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1307+2863_1307+288 others(24): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901577 | |||||||
| chr17:61901615 | T | C | 3 | a0001c0001t0002g0348 a0001c0001t0003g0243 a0001c0001t0003g0244 |
3 | HG02280.hp1 HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1307+2845A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901615 | |||||||
| chr17:61901631 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1307+2829C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901631 | |||||||
| chr17:61901775 | T | C | 1 | a0001c0001t0003g0182 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1307+2685A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901775 | |||||||
| chr17:61901786 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0214 a0001c0001t0001g0221 |
3 | HG02896.hp2 HG02897.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1307+2674G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901786 | |||||||
| chr17:61901817 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1307+2643G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901817 | |||||||
| chr17:61901873 | C | T | 3 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0016g0242 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1307+2587G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901873 | |||||||
| chr17:61901877 | C | T | 1 | a0001c0001t0002g0295 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1307+2583G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901877 | |||||||
| chr17:61901929 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1307+2531C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61901929 | |||||||
| chr17:61902151 | G | A | 19 | a0001c0001t0002g0330 a0001c0001t0002g0331 a0001c0001t0002g0333 others(16): Show |
19 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.1307+2309C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902151 | |||||||
| chr17:61902491 | C | A | 1 | a0001c0001t0005g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1307+1969G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902491 | |||||||
| chr17:61902518 | A | G | 1 | a0001c0001t0002g0263 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1307+1942T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902518 | |||||||
| chr17:61902567 | T | C | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1307+1893A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902567 | |||||||
| chr17:61902643 | G | T | 8 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0332 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1307+1817C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902643 | |||||||
| chr17:61902709 | T | TA | 22 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 others(19): Show |
22 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1307+1750dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902709 | |||||||
| chr17:61902858 | T | TA | 15 | a0001c0001t0001g0194 a0001c0001t0002g0095 a0001c0001t0002g0275 others(12): Show |
15 | HG01978.hp2 HG02056.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1307+1601dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902858 | |||||||
| chr17:61902858 | TA | T | 99 | a0001c0001t0001g0111 a0001c0001t0001g0123 a0001c0001t0001g0208 others(96): Show |
99 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(96): Show |
intron_variant | MODIFIER | c.1307+1601delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902858 | |||||||
| chr17:61902913 | T | A | 2 | a0001c0001t0001g0097 a0003c0009t0001g0140 |
2 | HG03017.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1307+1547A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902913 | |||||||
| chr17:61902937 | C | A | 12 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0005g0003 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1307+1523G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902937 | |||||||
| chr17:61902980 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1307+1480G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902980 | |||||||
| chr17:61902991 | C | T | 1 | a0001c0001t0002g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1307+1469G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61902991 | |||||||
| chr17:61903021 | C | T | 1 | a0001c0001t0014g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1307+1439G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903021 | |||||||
| chr17:61903162 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1307+1298C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903162 | |||||||
| chr17:61903174 | G | GA | 37 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0135 others(34): Show |
37 | HG00621.hp1 HG00621.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.1307+1285dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903174 | |||||||
| chr17:61903174 | GA | G | 45 | a0001c0001t0006g0107 a0001c0001t0007g0002 a0001c0002t0004g0039 others(42): Show |
45 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1307+1285delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903174 | |||||||
| chr17:61903220 | A | AT | 106 | a0001c0001t0001g0117 a0001c0001t0002g0033 a0001c0001t0002g0034 others(103): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.1307+1239dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903220 | |||||||
| chr17:61903262 | C | T | 4 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0193 others(1): Show |
4 | NA18994.hp1 NA19011.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307+1198G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903262 | |||||||
| chr17:61903398 | G | A | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307+1062C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903398 | |||||||
| chr17:61903612 | T | C | 2 | a0001c0002t0004g0061 a0001c0002t0004g0073 |
2 | HG01081.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1307+848A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903612 | |||||||
| chr17:61903665 | C | CA | 6 | a0001c0001t0001g0189 a0001c0001t0003g0021 a0001c0001t0003g0091 others(3): Show |
6 | HG02300.hp1 HG02630.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307+794dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903665 | |||||||
| chr17:61903665 | CA | C | 15 | a0001c0001t0001g0138 a0001c0001t0001g0214 a0001c0001t0002g0273 others(12): Show |
15 | HG02300.hp2 HG02735.hp1 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1307+794delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903665 | |||||||
| chr17:61903809 | G | C | 8 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0332 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1307+651C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61903809 | |||||||
| chr17:61904173 | T | C | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307+287A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61904173 | |||||||
| chr17:61904379 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0239 |
2 | HG02083.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.1307+81G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61904379 | |||||||
| chr17:61904405 | T | C | 1 | a0001c0002t0004g0070 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1307+55A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 9/24 | chr17 | 61904405 | |||||||
| chr17:61904627 | G | C | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1182-42C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61904627 | |||||||
| chr17:61904724 | G | A | 45 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.1182-139C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61904724 | |||||||
| chr17:61904946 | A | AT | 24 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(21): Show |
24 | HG00558.hp2 HG01934.hp2 HG01975.hp2 others(21): Show |
intron_variant | MODIFIER | c.1182-362dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61904946 | |||||||
| chr17:61904946 | AT | A | 123 | a0001c0001t0001g0106 a0001c0001t0002g0305 a0001c0001t0002g0334 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(120): Show |
intron_variant | MODIFIER | c.1182-362delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61904946 | |||||||
| chr17:61905160 | C | T | 52 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(49): Show |
52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1182-575G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905160 | |||||||
| chr17:61905225 | G | C | 1 | a0001c0002t0004g0070 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1182-640C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905225 | |||||||
| chr17:61905337 | T | C | 1 | a0001c0002t0011g0364 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1182-752A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905337 | |||||||
| chr17:61905359 | C | T | 52 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(49): Show |
52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1182-774G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905359 | |||||||
| chr17:61905513 | G | C | 1 | a0001c0001t0025g0326 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1182-928C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905513 | |||||||
| chr17:61905595 | G | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1182-1010C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905595 | |||||||
| chr17:61905695 | TTA | T | 5 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 others(2): Show |
5 | HG01109.hp2 HG01952.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1182-1112_1182-111 others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905695 | |||||||
| chr17:61905700 | T | C | 2 | a0001c0001t0003g0177 a0001c0001t0010g0238 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1182-1115A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905700 | |||||||
| chr17:61905754 | A | G | 1 | a0001c0001t0003g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1182-1169T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905754 | |||||||
| chr17:61905963 | C | G | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1182-1378G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905963 | |||||||
| chr17:61905965 | GGGATTAC others(6): Show |
G | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1182-1393_1182-138 others(17): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61905965 | |||||||
| chr17:61906001 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1181+1407G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906001 | |||||||
| chr17:61906364 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1181+1044G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906364 | |||||||
| chr17:61906507 | C | T | 1 | a0001c0001t0002g0299 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1181+901G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906507 | |||||||
| chr17:61906691 | A | C | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(43): Show |
46 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.1181+717T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906691 | |||||||
| chr17:61906830 | C | CA | 7 | a0001c0001t0001g0098 a0001c0001t0001g0141 a0001c0001t0006g0107 others(4): Show |
7 | HG02486.hp2 HG03834.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181+577dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906830 | |||||||
| chr17:61906830 | CA | C | 233 | a0001c0001t0001g0117 a0001c0001t0002g0033 a0001c0001t0002g0034 others(230): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1181+577delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906830 | |||||||
| chr17:61906910 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1181+498C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906910 | |||||||
| chr17:61906943 | G | A | 5 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 others(2): Show |
5 | HG01109.hp2 HG01952.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181+465C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906943 | |||||||
| chr17:61906963 | C | CA | 139 | a0001c0001t0001g0094 a0001c0001t0001g0098 a0001c0001t0001g0099 others(136): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.1181+444dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906963 | |||||||
| chr17:61906963 | C | CAA | 17 | a0001c0001t0001g0204 a0001c0001t0003g0051 a0001c0001t0003g0161 others(14): Show |
17 | HG00438.hp2 HG01175.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1181+443_1181+444d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906963 | |||||||
| chr17:61906963 | C | CAAA | 26 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(23): Show |
26 | HG00639.hp1 HG02055.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1181+442_1181+444d others(5): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906963 | |||||||
| chr17:61906963 | C | CAAAAAA | 85 | a0001c0001t0001g0117 a0001c0001t0002g0033 a0001c0001t0002g0034 others(82): Show |
85 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1181+439_1181+444d others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906963 | |||||||
| chr17:61906963 | C | CAAAAAAA | 22 | a0001c0001t0002g0037 a0001c0001t0002g0095 a0001c0001t0002g0264 others(19): Show |
22 | HG00140.hp2 HG00423.hp1 HG00621.hp1 others(19): Show |
intron_variant | MODIFIER | c.1181+438_1181+444d others(9): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906963 | |||||||
| chr17:61906985 | C | A | 2 | a0001c0001t0003g0358 a0001c0001t0007g0002 |
2 | HG01975.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1181+423G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61906985 | |||||||
| chr17:61907095 | C | T | 1 | a0001c0001t0002g0321 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1181+313G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61907095 | |||||||
| chr17:61907167 | T | A | 2 | a0001c0002t0004g0049 a0001c0002t0009g0048 |
2 | NA19058.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.1181+241A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61907167 | |||||||
| chr17:61907285 | C | A | 1 | a0001c0001t0008g0340 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1181+123G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 8/24 | chr17 | 61907285 | |||||||
| chr17:61907670 | T | A | 1 | a0001c0001t0012g0207 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.955-36A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61907670 | |||||||
| chr17:61907865 | A | T | 1 | a0006c0010t0002g0038 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.955-231T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61907865 | |||||||
| chr17:61907970 | G | A | 1 | a0001c0001t0003g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.955-336C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61907970 | |||||||
| chr17:61908329 | C | T | 45 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.955-695G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908329 | |||||||
| chr17:61908424 | C | A | 2 | a0001c0001t0003g0032 a0001c0001t0003g0252 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.955-790G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908424 | |||||||
| chr17:61908473 | A | C | 4 | a0001c0001t0008g0336 a0001c0001t0008g0338 a0001c0001t0008g0339 others(1): Show |
4 | HG03491.hp1 HG03492.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.955-839T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908473 | |||||||
| chr17:61908502 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.955-868A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908502 | |||||||
| chr17:61908569 | T | C | 1 | a0001c0001t0002g0301 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.955-935A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908569 | |||||||
| chr17:61908814 | T | TAAAATCA others(305): Show |
1 | a0001c0002t0011g0363 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.955-1181_955-1180i others(314): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908814 | |||||||
| chr17:61908814 | T | TAAAATCA others(305): Show |
42 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(39): Show |
42 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.955-1181_955-1180i others(314): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908814 | |||||||
| chr17:61908814 | T | TAAAATCA others(306): Show |
9 | a0001c0002t0004g0056 a0001c0002t0004g0058 a0001c0002t0004g0066 others(6): Show |
9 | HG01175.hp1 HG02056.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.955-1181_955-1180i others(315): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908814 | |||||||
| chr17:61908860 | A | T | 1 | a0001c0001t0006g0093 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.955-1226T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908860 | |||||||
| chr17:61908915 | TGTTGTCT others(18): Show |
T | 1 | a0001c0001t0001g0209 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.955-1306_955-1282d others(27): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908915 | |||||||
| chr17:61908961 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.955-1327A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61908961 | |||||||
| chr17:61909121 | C | CT | 46 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(43): Show |
46 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.955-1488dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909121 | |||||||
| chr17:61909435 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.955-1801C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909435 | |||||||
| chr17:61909554 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.955-1920G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909554 | |||||||
| chr17:61909611 | T | A | 1 | a0001c0002t0011g0365 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.954+1909A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909611 | |||||||
| chr17:61909632 | C | T | 52 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(49): Show |
52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.954+1888G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909632 | |||||||
| chr17:61909769 | G | A | 1 | a0001c0001t0002g0311 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.954+1751C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909769 | |||||||
| chr17:61909779 | T | C | 1 | a0001c0001t0014g0144 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.954+1741A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909779 | |||||||
| chr17:61909802 | C | T | 2 | a0001c0001t0005g0007 a0001c0001t0005g0011 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.954+1718G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909802 | |||||||
| chr17:61909811 | G | A | 110 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(107): Show |
110 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.954+1709C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909811 | |||||||
| chr17:61909815 | A | ATATATAC others(3): Show |
20 | a0001c0001t0002g0261 a0001c0001t0002g0267 a0001c0001t0002g0271 others(17): Show |
20 | HG00558.hp1 HG02071.hp2 HG02129.hp1 others(17): Show |
intron_variant | MODIFIER | c.954+1704_954+1705i others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909815 | |||||||
| chr17:61909815 | A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0209 a0001c0001t0002g0296 |
2 | NA18991.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.954+1704_954+1705i others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909815 | |||||||
| chr17:61909815 | ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.954+1693_954+1704d others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909815 | |||||||
| chr17:61909816 | T | TATATAC | 81 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(78): Show |
81 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.954+1703_954+1704i others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909816 | |||||||
| chr17:61909817 | G | A | 6 | a0001c0001t0002g0312 a0001c0001t0002g0331 a0001c0001t0002g0360 others(3): Show |
6 | HG01081.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+1703C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909817 | |||||||
| chr17:61909818 | T | TATAC | 6 | a0001c0001t0002g0312 a0001c0001t0002g0331 a0001c0001t0002g0360 others(3): Show |
6 | HG01081.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+1701_954+1702i others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909818 | |||||||
| chr17:61909819 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.954+1701C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909819 | |||||||
| chr17:61909821 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.954+1699C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909821 | |||||||
| chr17:61909823 | A | ACATGTG | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+1696_954+1697i others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | |||||||
| chr17:61909823 | A | ATG | 3 | a0001c0001t0001g0147 a0001c0001t0001g0204 a0001c0001t0001g0215 |
3 | HG01168.hp2 HG01358.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.954+1695_954+1696d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | |||||||
| chr17:61909823 | A | G | 90 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(87): Show |
90 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.954+1697T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | |||||||
| chr17:61909823 | ATG | A | 33 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0103 others(30): Show |
33 | HG00280.hp1 HG00544.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.954+1695_954+1696d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | |||||||
| chr17:61909823 | ATGTG | A | 108 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0102 others(105): Show |
108 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.954+1693_954+1696d others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | |||||||
| chr17:61909823 | ATGTGTG | A | 13 | a0001c0001t0003g0020 a0001c0001t0003g0023 a0001c0001t0003g0028 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.954+1691_954+1696d others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | |||||||
| chr17:61909823 | ATGTGTGT others(1): Show |
A | 59 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0001t0003g0016 others(56): Show |
59 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(56): Show |
intron_variant | MODIFIER | c.954+1689_954+1696d others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | |||||||
| chr17:61909823 | ATGTGTGT others(3): Show |
A | 5 | a0001c0001t0001g0257 a0001c0001t0005g0003 a0001c0001t0005g0004 others(2): Show |
5 | HG02004.hp2 HG02055.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.954+1687_954+1696d others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909823 | |||||||
| chr17:61909824 | T | C | 18 | a0001c0001t0001g0209 a0001c0001t0002g0261 a0001c0001t0002g0262 others(15): Show |
18 | HG00558.hp1 HG00673.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.954+1696A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909824 | |||||||
| chr17:61909826 | T | TAC | 64 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(61): Show |
64 | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.954+1693_954+1694i others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909826 | |||||||
| chr17:61909827 | G | A | 21 | a0001c0001t0002g0095 a0001c0001t0002g0330 a0001c0001t0002g0335 others(18): Show |
21 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.954+1693C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909827 | |||||||
| chr17:61909828 | T | C | 17 | a0001c0001t0002g0095 a0001c0001t0002g0330 a0001c0001t0002g0335 others(14): Show |
17 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.954+1692A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909828 | |||||||
| chr17:61909829 | G | A | 6 | a0001c0001t0002g0312 a0001c0001t0002g0331 a0001c0001t0002g0360 others(3): Show |
6 | HG01081.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+1691C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909829 | |||||||
| chr17:61909830 | T | C | 6 | a0001c0001t0002g0312 a0001c0001t0002g0331 a0001c0001t0002g0360 others(3): Show |
6 | HG01081.hp1 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+1690A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909830 | |||||||
| chr17:61909835 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.954+1685C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909835 | |||||||
| chr17:61909836 | T | C | 1 | a0001c0001t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.954+1684A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909836 | |||||||
| chr17:61909915 | T | A | 9 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0332 others(6): Show |
9 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.954+1605A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61909915 | |||||||
| chr17:61910006 | T | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.954+1514A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910006 | |||||||
| chr17:61910200 | C | T | 9 | a0001c0002t0004g0050 a0001c0002t0004g0058 a0001c0002t0004g0063 others(6): Show |
9 | NA18945.hp2 NA18948.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.954+1320G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910200 | |||||||
| chr17:61910369 | G | A | 1 | a0001c0001t0002g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.954+1151C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910369 | |||||||
| chr17:61910417 | G | A | 110 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(107): Show |
110 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.954+1103C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910417 | |||||||
| chr17:61910453 | T | TGAG | 5 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 others(2): Show |
5 | HG01109.hp2 HG01952.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.954+1066_954+1067i others(5): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910453 | |||||||
| chr17:61910511 | G | A | 1 | a0001c0002t0004g0049 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.954+1009C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910511 | |||||||
| chr17:61910553 | T | C | 4 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0166 others(1): Show |
4 | HG02280.hp2 HG03490.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.954+967A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910553 | |||||||
| chr17:61910583 | C | A | 45 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0088 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.954+937G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910583 | |||||||
| chr17:61910591 | C | CA | 105 | a0001c0001t0001g0117 a0001c0001t0001g0189 a0001c0001t0001g0209 others(102): Show |
105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.954+928dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910591 | |||||||
| chr17:61910591 | C | CAA | 11 | a0001c0001t0001g0213 a0001c0001t0002g0272 a0001c0001t0002g0279 others(8): Show |
11 | HG01106.hp1 HG01175.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.954+927_954+928dup others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910591 | |||||||
| chr17:61910645 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.954+875G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910645 | |||||||
| chr17:61910756 | A | C | 1 | a0001c0001t0002g0312 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.954+764T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910756 | |||||||
| chr17:61910767 | TATA | T | 8 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0332 others(5): Show |
8 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.954+750_954+752del others(3): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910767 | |||||||
| chr17:61910885 | G | A | 1 | a0001c0002t0004g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.954+635C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 7/24 | chr17 | 61910885 | |||||||
| chr17:61911765 | A | C | 109 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(106): Show |
109 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.781-72T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 6/24 | chr17 | 61911765 | |||||||
| chr17:61912212 | T | A | 1 | a0001c0004t0002g0308 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.650-142A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912212 | |||||||
| chr17:61912217 | A | G | 1 | a0001c0004t0002g0308 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.650-147T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912217 | |||||||
| chr17:61912220 | A | G | 1 | a0001c0004t0002g0308 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.650-150T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912220 | |||||||
| chr17:61912221 | A | T | 1 | a0001c0004t0002g0308 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.650-151T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912221 | |||||||
| chr17:61912339 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.650-269C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912339 | |||||||
| chr17:61912373 | CG | C | 224 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0098 others(221): Show |
224 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.650-304delC | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912373 | |||||||
| chr17:61912373 | CGG | C | 99 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0103 others(96): Show |
99 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.650-305_650-304del others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912373 | |||||||
| chr17:61912375 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.650-305C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912375 | |||||||
| chr17:61912384 | G | C | 1 | a0001c0002t0028g0366 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.650-314C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912384 | |||||||
| chr17:61912385 | G | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.650-315C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912385 | |||||||
| chr17:61912385 | G | T | 22 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(19): Show |
22 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.650-315C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912385 | |||||||
| chr17:61912391 | G | A | 3 | a0001c0002t0004g0061 a0001c0002t0004g0068 a0001c0002t0004g0073 |
3 | HG01081.hp2 HG02258.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.650-321C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912391 | |||||||
| chr17:61912415 | G | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.650-345C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912415 | |||||||
| chr17:61912520 | C | G | 110 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(107): Show |
110 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.650-450G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912520 | |||||||
| chr17:61912681 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.650-611A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912681 | |||||||
| chr17:61912706 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.650-636A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912706 | |||||||
| chr17:61912789 | T | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.650-719A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912789 | |||||||
| chr17:61912865 | T | C | 363 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0096 others(360): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.650-795A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912865 | |||||||
| chr17:61912907 | C | A | 1 | a0001c0001t0003g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.650-837G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912907 | |||||||
| chr17:61912946 | C | A | 1 | a0001c0001t0007g0351 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.650-876G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912946 | |||||||
| chr17:61912946 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.650-876G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912946 | |||||||
| chr17:61912953 | A | G | 253 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.650-883T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912953 | |||||||
| chr17:61912968 | C | G | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.650-898G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61912968 | |||||||
| chr17:61913045 | C | T | 3 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0016g0242 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.650-975G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913045 | |||||||
| chr17:61913112 | C | T | 1 | a0001c0002t0004g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.650-1042G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913112 | |||||||
| chr17:61913248 | G | A | 52 | a0001c0002t0004g0039 a0001c0002t0004g0040 a0001c0002t0004g0041 others(49): Show |
52 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.650-1178C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913248 | |||||||
| chr17:61913283 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.650-1213C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913283 | |||||||
| chr17:61913342 | C | CA | 9 | a0001c0001t0001g0241 a0001c0001t0002g0315 a0001c0001t0003g0031 others(6): Show |
9 | HG00597.hp1 HG01175.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.650-1273dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913342 | |||||||
| chr17:61913362 | A | AG | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.650-1293dupC | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913362 | |||||||
| chr17:61913373 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.650-1303C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913373 | |||||||
| chr17:61913382 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.650-1312C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913382 | |||||||
| chr17:61913462 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.650-1392T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61913462 | |||||||
| chr17:61914048 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.650-1978A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914048 | |||||||
| chr17:61914106 | A | G | 1 | a0001c0001t0002g0297 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.650-2036T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914106 | |||||||
| chr17:61914338 | C | T | 1 | a0001c0001t0002g0334 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.650-2268G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914338 | |||||||
| chr17:61914515 | C | T | 1 | a0002c0005t0001g0086 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.650-2445G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914515 | |||||||
| chr17:61914571 | C | T | 78 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(75): Show |
78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.650-2501G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914571 | |||||||
| chr17:61914573 | G | A | 6 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0145 others(3): Show |
6 | HG02622.hp1 HG02922.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.650-2503C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914573 | |||||||
| chr17:61914692 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.650-2622C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914692 | |||||||
| chr17:61914702 | C | CA | 47 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0154 others(44): Show |
47 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.650-2633dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | |||||||
| chr17:61914702 | C | CAA | 6 | a0001c0001t0001g0145 a0001c0001t0001g0150 a0001c0001t0001g0193 others(3): Show |
6 | HG02602.hp2 HG03130.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.650-2634_650-2633d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | |||||||
| chr17:61914702 | C | CAAAAAAA others(3): Show |
2 | a0001c0003t0002g0012 a0001c0003t0002g0013 |
2 | HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.650-2642_650-2633d others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | |||||||
| chr17:61914702 | C | CAAAAAAA others(4): Show |
7 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0332 others(4): Show |
7 | HG02257.hp2 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.650-2643_650-2633d others(13): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | |||||||
| chr17:61914702 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0002g0334 a0001c0001t0002g0347 a0001c0001t0002g0348 others(1): Show |
4 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.650-2644_650-2633d others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | |||||||
| chr17:61914702 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.650-2645_650-2633d others(15): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | |||||||
| chr17:61914702 | CA | C | 13 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0002g0095 others(10): Show |
13 | HG00558.hp2 HG01167.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.650-2633delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914702 | |||||||
| chr17:61914873 | C | CA | 9 | a0001c0001t0001g0105 a0001c0001t0001g0189 a0001c0001t0001g0254 others(6): Show |
9 | HG01192.hp2 HG01346.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.650-2804dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61914873 | |||||||
| chr17:61915067 | G | A | 104 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(101): Show |
104 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.650-2997C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915067 | |||||||
| chr17:61915165 | C | T | 2 | a0001c0001t0003g0032 a0001c0001t0003g0252 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.650-3095G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915165 | |||||||
| chr17:61915195 | G | A | 44 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(41): Show |
44 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.650-3125C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915195 | |||||||
| chr17:61915333 | G | A | 2 | a0001c0001t0005g0007 a0001c0001t0005g0011 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.650-3263C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915333 | |||||||
| chr17:61915341 | A | AAAAT | 70 | a0001c0001t0001g0109 a0001c0001t0001g0117 a0001c0001t0001g0186 others(67): Show |
70 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.650-3275_650-3272d others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | |||||||
| chr17:61915341 | A | AAAATAAA others(1): Show |
8 | a0001c0001t0003g0023 a0001c0001t0003g0025 a0001c0001t0003g0026 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.650-3279_650-3272d others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | |||||||
| chr17:61915341 | A | AAAATAAA others(5): Show |
11 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(8): Show |
11 | HG00639.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.650-3283_650-3272d others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | |||||||
| chr17:61915341 | A | AAAATAAA others(9): Show |
1 | a0001c0001t0003g0016 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.650-3287_650-3272d others(18): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | |||||||
| chr17:61915341 | A | T | 1 | a0001c0001t0001g0202 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.650-3271T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | |||||||
| chr17:61915341 | AAAAT | A | 105 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(102): Show |
105 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.650-3275_650-3272d others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915341 | |||||||
| chr17:61915414 | A | T | 205 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(202): Show |
205 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.650-3344T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915414 | |||||||
| chr17:61915489 | G | A | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.650-3419C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915489 | |||||||
| chr17:61915536 | A | AC | 4 | a0001c0001t0002g0287 a0001c0001t0002g0307 a0001c0001t0002g0323 others(1): Show |
4 | HG02083.hp1 HG02132.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.650-3467_650-3466i others(3): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915536 | |||||||
| chr17:61915536 | A | C | 101 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(98): Show |
101 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.650-3466T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915536 | |||||||
| chr17:61915547 | G | A | 21 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(18): Show |
21 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.650-3477C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915547 | |||||||
| chr17:61915655 | TA | T | 249 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0096 others(246): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.650-3586delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915655 | |||||||
| chr17:61915661 | A | T | 1 | a0001c0002t0004g0050 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.650-3591T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915661 | |||||||
| chr17:61915688 | G | A | 15 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0332 others(12): Show |
15 | HG02109.hp2 HG02258.hp1 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.650-3618C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915688 | |||||||
| chr17:61915724 | G | A | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.650-3654C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915724 | |||||||
| chr17:61915781 | G | C | 3 | a0001c0002t0004g0074 a0001c0002t0004g0079 a0001c0002t0004g0081 |
3 | NA18967.hp2 NA19007.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.649+3619C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915781 | |||||||
| chr17:61915796 | C | T | 7 | a0001c0002t0004g0044 a0001c0002t0004g0045 a0001c0002t0004g0047 others(4): Show |
7 | HG00438.hp2 NA18963.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.649+3604G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915796 | |||||||
| chr17:61915801 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.649+3599C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915801 | |||||||
| chr17:61915807 | G | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.649+3593C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915807 | |||||||
| chr17:61915816 | T | TA | 127 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0097 others(124): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(124): Show |
intron_variant | MODIFIER | c.649+3583dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915816 | |||||||
| chr17:61915816 | T | TAA | 12 | a0001c0001t0001g0094 a0001c0001t0001g0111 a0001c0001t0001g0145 others(9): Show |
12 | HG01978.hp1 HG02630.hp1 HG02738.hp2 others(9): Show |
intron_variant | MODIFIER | c.649+3582_649+3583d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915816 | |||||||
| chr17:61915816 | TA | T | 12 | a0001c0001t0001g0129 a0001c0001t0002g0305 a0001c0001t0002g0332 others(9): Show |
12 | HG01167.hp2 HG02145.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.649+3583delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915816 | |||||||
| chr17:61915816 | TAAAAAAA others(4): Show |
T | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.649+3573_649+3583d others(13): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915816 | |||||||
| chr17:61915817 | A | G | 2 | a0001c0001t0003g0176 a0001c0001t0003g0237 |
2 | HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.649+3583T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61915817 | |||||||
| chr17:61916204 | G | C | 1 | a0001c0001t0007g0351 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.649+3196C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916204 | |||||||
| chr17:61916385 | G | A | 205 | a0001c0001t0001g0209 a0001c0001t0002g0033 a0001c0001t0002g0034 others(202): Show |
205 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.649+3015C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916385 | |||||||
| chr17:61916411 | T | C | 1 | a0002c0005t0001g0086 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.649+2989A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916411 | |||||||
| chr17:61916460 | C | A | 3 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0016g0242 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.649+2940G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916460 | |||||||
| chr17:61916772 | T | C | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.649+2628A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916772 | |||||||
| chr17:61916983 | G | A | 10 | a0001c0001t0002g0328 a0001c0001t0002g0329 a0001c0001t0002g0332 others(7): Show |
10 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.649+2417C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61916983 | |||||||
| chr17:61917262 | C | T | 21 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(18): Show |
21 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.649+2138G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61917262 | |||||||
| chr17:61917796 | TA | T | 5 | a0001c0001t0002g0330 a0001c0001t0002g0333 a0001c0001t0002g0335 others(2): Show |
5 | HG00140.hp2 HG01099.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.649+1603delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61917796 | |||||||
| chr17:61918099 | T | C | 9 | a0001c0001t0003g0157 a0001c0001t0003g0160 a0001c0001t0003g0164 others(6): Show |
9 | HG00408.hp1 NA18951.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.649+1301A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918099 | |||||||
| chr17:61918254 | T | C | 1 | a0001c0001t0005g0009 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.649+1146A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918254 | |||||||
| chr17:61918311 | G | A | 2 | a0001c0001t0005g0007 a0001c0001t0005g0011 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.649+1089C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918311 | |||||||
| chr17:61918543 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.649+857C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918543 | |||||||
| chr17:61918631 | A | G | 106 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(103): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.649+769T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918631 | |||||||
| chr17:61918818 | G | C | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.649+582C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918818 | |||||||
| chr17:61918906 | T | C | 2 | a0001c0002t0004g0064 a0001c0002t0004g0077 |
2 | NA19079.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.649+494A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918906 | |||||||
| chr17:61918916 | C | A | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.649+484G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918916 | |||||||
| chr17:61918923 | G | GT | 37 | a0001c0001t0001g0111 a0001c0001t0001g0113 a0001c0001t0001g0116 others(34): Show |
37 | HG00140.hp1 HG00438.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.649+476dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918923 | |||||||
| chr17:61918923 | GT | G | 97 | a0001c0001t0001g0146 a0001c0001t0001g0192 a0001c0001t0001g0204 others(94): Show |
97 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.649+476delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918923 | |||||||
| chr17:61918945 | G | A | 1 | a0001c0001t0003g0358 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.649+455C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918945 | |||||||
| chr17:61918994 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.649+406C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61918994 | |||||||
| chr17:61919155 | C | A | 4 | a0001c0002t0004g0082 a0001c0002t0004g0083 a0001c0002t0004g0084 others(1): Show |
4 | NA18950.hp2 NA19060.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.649+245G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61919155 | |||||||
| chr17:61919215 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.649+185C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 5/24 | chr17 | 61919215 | |||||||
| chr17:61919573 | C | T | 2 | a0001c0001t0002g0328 a0001c0001t0002g0332 |
2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.536-60G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61919573 | |||||||
| chr17:61919821 | T | C | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0036 others(1): Show |
4 | HG02027.hp2 NA18993.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.536-308A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61919821 | |||||||
| chr17:61919990 | G | A | 10 | a0001c0001t0003g0032 a0001c0001t0003g0173 a0001c0001t0003g0174 others(7): Show |
10 | HG02257.hp1 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.536-477C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61919990 | |||||||
| chr17:61920052 | A | G | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.536-539T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920052 | |||||||
| chr17:61920120 | A | G | 20 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(17): Show |
20 | HG00558.hp2 HG02083.hp2 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.536-607T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920120 | |||||||
| chr17:61920180 | C | CT | 62 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0098 others(59): Show |
62 | HG00639.hp1 HG00642.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.536-668dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920180 | |||||||
| chr17:61920180 | C | CTT | 85 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(82): Show |
85 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.536-669_536-668dup others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920180 | |||||||
| chr17:61920180 | C | CTTT | 13 | a0001c0001t0002g0036 a0001c0001t0002g0261 a0001c0001t0002g0267 others(10): Show |
13 | HG00558.hp1 HG00597.hp2 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.536-670_536-668dup others(3): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920180 | |||||||
| chr17:61920198 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.536-685A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920198 | |||||||
| chr17:61920200 | C | T | 7 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0003g0179 others(4): Show |
7 | HG01346.hp2 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.536-687G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920200 | |||||||
| chr17:61920280 | C | T | 1 | a0001c0001t0002g0300 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.536-767G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920280 | |||||||
| chr17:61920486 | C | CT | 39 | a0001c0001t0001g0096 a0001c0001t0001g0102 a0001c0001t0001g0108 others(36): Show |
39 | HG00280.hp2 HG01071.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.536-974dupA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920486 | |||||||
| chr17:61920486 | CT | C | 150 | a0001c0001t0001g0124 a0001c0001t0001g0129 a0001c0001t0001g0130 others(147): Show |
150 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.536-974delA | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920486 | |||||||
| chr17:61920486 | CTT | C | 21 | a0001c0001t0002g0035 a0001c0001t0002g0261 a0001c0001t0002g0266 others(18): Show |
21 | HG00544.hp1 HG00639.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.536-975_536-974del others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920486 | |||||||
| chr17:61920499 | T | G | 16 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.536-986A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920499 | |||||||
| chr17:61920504 | T | G | 16 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.536-991A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920504 | |||||||
| chr17:61920526 | C | T | 53 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0002t0004g0039 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.536-1013G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920526 | |||||||
| chr17:61920580 | C | A | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.536-1067G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920580 | |||||||
| chr17:61920622 | G | A | 26 | a0001c0001t0002g0287 a0001c0001t0002g0288 a0001c0001t0002g0289 others(23): Show |
26 | HG00673.hp1 HG01928.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.535+1103C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920622 | |||||||
| chr17:61920789 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+936A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920789 | |||||||
| chr17:61920791 | A | G | 1 | a0001c0001t0003g0358 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.535+934T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920791 | |||||||
| chr17:61920793 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+932T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920793 | |||||||
| chr17:61920796 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+929G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920796 | |||||||
| chr17:61920802 | CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+906_535+922del others(17): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920802 | |||||||
| chr17:61920821 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+904G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920821 | |||||||
| chr17:61920826 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+899A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920826 | |||||||
| chr17:61920828 | T | A | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+897A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920828 | |||||||
| chr17:61920831 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+894T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920831 | |||||||
| chr17:61920832 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+893G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920832 | |||||||
| chr17:61920833 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+892T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920833 | |||||||
| chr17:61920841 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+884T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920841 | |||||||
| chr17:61920846 | A | T | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+879T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920846 | |||||||
| chr17:61920847 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+878G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920847 | |||||||
| chr17:61920848 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+877T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920848 | |||||||
| chr17:61920865 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+860C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920865 | |||||||
| chr17:61920872 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+853A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920872 | |||||||
| chr17:61920876 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+849G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920876 | |||||||
| chr17:61920877 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+848G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920877 | |||||||
| chr17:61920878 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+847T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920878 | |||||||
| chr17:61920909 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+816G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920909 | |||||||
| chr17:61920910 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+815T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920910 | |||||||
| chr17:61920929 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+796A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920929 | |||||||
| chr17:61920933 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.535+792G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61920933 | |||||||
| chr17:61921373 | C | A | 102 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0096 others(99): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.535+352G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61921373 | |||||||
| chr17:61921492 | T | C | 2 | a0001c0001t0002g0344 a0001c0001t0002g0353 |
2 | HG00438.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.535+233A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61921492 | |||||||
| chr17:61921591 | C | G | 7 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
7 | NA18949.hp1 NA18952.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.535+134G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61921591 | |||||||
| chr17:61921670 | G | A | 9 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.535+55C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 4/24 | chr17 | 61921670 | |||||||
| chr17:61922029 | T | C | 106 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(103): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.433-202A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922029 | |||||||
| chr17:61922352 | TAGCTACT others(1): Show |
T | 93 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(90): Show |
93 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.433-533_433-526del others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922352 | |||||||
| chr17:61922383 | G | T | 1 | a0001c0001t0003g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.433-556C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922383 | |||||||
| chr17:61922444 | G | T | 21 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(18): Show |
21 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.433-617C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922444 | |||||||
| chr17:61922467 | CA | C | 95 | a0001c0001t0001g0097 a0001c0001t0001g0129 a0001c0001t0001g0130 others(92): Show |
95 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.433-641delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922467 | |||||||
| chr17:61922511 | C | CAT | 20 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0105 others(17): Show |
20 | HG00408.hp2 HG00597.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.433-686_433-685dup others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | C | CATAT | 14 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0143 others(11): Show |
14 | HG00280.hp1 HG01168.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.433-688_433-685dup others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | C | CATATAT | 17 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0212 others(14): Show |
17 | HG00642.hp2 HG00733.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-690_433-685dup others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | C | CATATATA others(1): Show |
30 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0098 others(27): Show |
30 | HG01074.hp1 HG01167.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.433-692_433-685dup others(8): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | C | CATATATA others(3): Show |
49 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(46): Show |
49 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.433-694_433-685dup others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | C | CATATATA others(5): Show |
34 | a0001c0001t0001g0097 a0001c0001t0001g0115 a0001c0001t0001g0116 others(31): Show |
34 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.433-696_433-685dup others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | C | CATATATA others(7): Show |
23 | a0001c0001t0001g0102 a0001c0001t0001g0112 a0001c0001t0001g0113 others(20): Show |
23 | HG00140.hp2 HG01081.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.433-698_433-685dup others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | C | CATATATA others(9): Show |
15 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0197 others(12): Show |
15 | HG00621.hp2 HG01516.hp2 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.433-700_433-685dup others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | C | CATATATA others(11): Show |
13 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0195 others(10): Show |
13 | HG00621.hp1 HG00673.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.433-702_433-685dup others(18): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | C | CATATATA others(13): Show |
4 | a0001c0001t0002g0287 a0001c0001t0002g0288 a0001c0001t0002g0289 others(1): Show |
4 | HG01993.hp1 HG02083.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-704_433-685dup others(20): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | C | CATATATA others(15): Show |
2 | a0001c0001t0002g0184 a0001c0001t0002g0310 |
2 | NA18985.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.433-706_433-685dup others(22): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | CAT | C | 8 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-686_433-685del others(2): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | CATAT | C | 3 | a0001c0001t0002g0306 a0001c0001t0002g0307 a0001c0001t0005g0007 |
3 | HG02132.hp1 HG03453.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.433-688_433-685del others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | CATATAT | C | 3 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0352 |
3 | HG01106.hp1 HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.433-690_433-685del others(6): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | CATATATA others(3): Show |
C | 4 | a0001c0001t0001g0222 a0001c0002t0004g0066 a0001c0002t0011g0363 others(1): Show |
4 | HG01175.hp1 HG02080.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-694_433-685del others(10): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | CATATATA others(5): Show |
C | 58 | a0001c0001t0001g0154 a0001c0001t0003g0051 a0001c0001t0003g0052 others(55): Show |
58 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.433-696_433-685del others(12): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | CATATATA others(7): Show |
C | 29 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0163 others(26): Show |
29 | HG00099.hp2 HG00140.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.433-698_433-685del others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | CATATATA others(9): Show |
C | 2 | a0001c0001t0002g0286 a0001c0001t0025g0326 |
2 | HG01928.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.433-700_433-685del others(16): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | CATATATA others(11): Show |
C | 6 | a0001c0001t0002g0344 a0001c0001t0002g0353 a0001c0003t0002g0012 others(3): Show |
6 | HG00438.hp1 HG00597.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-702_433-685del others(18): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922511 | CATATATA others(13): Show |
C | 21 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(18): Show |
21 | HG00639.hp1 HG01109.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.433-704_433-685del others(20): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922511 | |||||||
| chr17:61922543 | T | TATATATA others(7): Show |
1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.433-717_433-716ins others(14): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922543 | |||||||
| chr17:61922547 | C | T | 6 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | NA18612.hp1 NA18946.hp1 NA18994.hp1 others(3): Show |
intron_variant | MODIFIER | c.433-720G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922547 | |||||||
| chr17:61922548 | G | A | 214 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(211): Show |
214 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.433-721C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922548 | |||||||
| chr17:61922611 | T | C | 28 | a0001c0001t0002g0095 a0001c0001t0002g0287 a0001c0001t0002g0288 others(25): Show |
28 | HG00673.hp1 HG01928.hp2 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.433-784A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922611 | |||||||
| chr17:61922676 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.433-849T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922676 | |||||||
| chr17:61922747 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.433-920C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61922747 | |||||||
| chr17:61923079 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.433-1252T>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923079 | |||||||
| chr17:61923098 | T | A | 2 | a0001c0001t0005g0007 a0001c0001t0005g0011 |
2 | HG02145.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.433-1271A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923098 | |||||||
| chr17:61923145 | T | C | 2 | a0001c0001t0002g0035 a0006c0010t0002g0038 |
2 | NA19074.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.433-1318A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923145 | |||||||
| chr17:61923214 | G | A | 3 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0016g0242 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.433-1387C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923214 | |||||||
| chr17:61923215 | T | C | 3 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0016g0242 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.433-1388A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923215 | |||||||
| chr17:61923263 | A | G | 3 | a0001c0001t0003g0243 a0001c0001t0003g0244 a0001c0001t0016g0242 |
3 | HG02280.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.433-1436T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923263 | |||||||
| chr17:61923273 | C | T | 1 | a0001c0001t0002g0261 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.433-1446G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923273 | |||||||
| chr17:61923278 | C | T | 9 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(6): Show |
9 | HG02451.hp1 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-1451G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923278 | |||||||
| chr17:61923280 | A | G | 1 | a0001c0001t0003g0025 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-1453T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923280 | |||||||
| chr17:61923288 | T | C | 106 | a0001c0001t0001g0097 a0001c0001t0001g0239 a0001c0001t0002g0033 others(103): Show |
106 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.433-1461A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923288 | |||||||
| chr17:61923305 | G | A | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0240 others(1): Show |
4 | HG00408.hp2 HG00597.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-1478C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923305 | |||||||
| chr17:61923401 | C | CGGGAGGC others(10): Show |
1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.432+1543_432+1559d others(19): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923401 | |||||||
| chr17:61923409 | G | A | 1 | a0001c0001t0003g0187 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.432+1552C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923409 | |||||||
| chr17:61923425 | C | T | 9 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(6): Show |
9 | HG01070.hp1 HG01255.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.432+1536G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923425 | |||||||
| chr17:61923450 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.432+1511G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923450 | |||||||
| chr17:61923477 | C | CA | 121 | a0001c0001t0001g0094 a0001c0001t0001g0188 a0001c0001t0001g0189 others(118): Show |
121 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.432+1483dupT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923477 | |||||||
| chr17:61923477 | C | CAA | 14 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0002g0327 others(11): Show |
14 | HG00733.hp1 HG00733.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.432+1482_432+1483d others(4): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923477 | |||||||
| chr17:61923477 | CA | C | 7 | a0001c0001t0001g0096 a0001c0001t0003g0091 a0001c0002t0004g0039 others(4): Show |
7 | HG00642.hp1 HG01433.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+1483delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923477 | |||||||
| chr17:61923665 | G | A | 4 | a0001c0003t0002g0012 a0001c0003t0002g0013 a0001c0003t0002g0014 others(1): Show |
4 | HG02257.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+1296C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923665 | |||||||
| chr17:61923674 | T | TGTG | 53 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0002t0004g0039 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.432+1284_432+1286d others(5): Show |
INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923674 | |||||||
| chr17:61923686 | G | T | 106 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(103): Show |
106 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.432+1275C>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923686 | |||||||
| chr17:61923689 | T | G | 1 | a0001c0002t0004g0081 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.432+1272A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923689 | |||||||
| chr17:61923750 | G | A | 4 | a0001c0002t0004g0082 a0001c0002t0004g0083 a0001c0002t0004g0084 others(1): Show |
4 | NA18950.hp2 NA19060.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+1211C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923750 | |||||||
| chr17:61923945 | G | A | 1 | a0001c0001t0010g0250 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.432+1016C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61923945 | |||||||
| chr17:61924030 | A | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0006g0093 |
3 | NA18985.hp1 NA19005.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.432+931T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924030 | |||||||
| chr17:61924244 | T | C | 1 | a0001c0001t0003g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.432+717A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924244 | |||||||
| chr17:61924293 | T | A | 2 | a0001c0001t0003g0032 a0001c0001t0003g0252 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.432+668A>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924293 | |||||||
| chr17:61924483 | A | G | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.432+478T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924483 | |||||||
| chr17:61924546 | C | T | 75 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(72): Show |
75 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.432+415G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924546 | |||||||
| chr17:61924556 | T | G | 8 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.432+405A>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924556 | |||||||
| chr17:61924600 | C | T | 1 | a0001c0001t0003g0091 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.432+361G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924600 | |||||||
| chr17:61924617 | G | A | 108 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(105): Show |
108 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.432+344C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924617 | |||||||
| chr17:61924679 | A | G | 3 | a0001c0001t0003g0088 a0001c0001t0003g0089 a0001c0001t0003g0090 |
3 | HG02717.hp2 HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.432+282T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924679 | |||||||
| chr17:61924698 | G | A | 1 | a0001c0001t0002g0355 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.432+263C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924698 | |||||||
| chr17:61924722 | A | C | 1 | a0001c0001t0004g0087 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.432+239T>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924722 | |||||||
| chr17:61924937 | G | A | 4 | a0001c0002t0004g0082 a0001c0002t0004g0083 a0001c0002t0004g0084 others(1): Show |
4 | NA18950.hp2 NA19060.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+24C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 3/24 | chr17 | 61924937 | |||||||
| chr17:61925433 | C | T | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.294-334G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925433 | |||||||
| chr17:61925526 | G | C | 1 | a0001c0001t0007g0356 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.294-427C>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925526 | |||||||
| chr17:61925737 | C | T | 53 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0002t0004g0039 others(50): Show |
53 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.293+615G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925737 | |||||||
| chr17:61925820 | T | C | 1 | a0001c0001t0003g0357 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.293+532A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925820 | |||||||
| chr17:61925882 | C | G | 6 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(3): Show |
6 | HG02027.hp2 NA18993.hp1 NA19063.hp2 others(3): Show |
intron_variant | MODIFIER | c.293+470G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925882 | |||||||
| chr17:61925957 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.293+395G>A | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925957 | |||||||
| chr17:61925966 | C | A | 1 | a0001c0001t0003g0358 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.293+386G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61925966 | |||||||
| chr17:61926033 | GA | G | 16 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(13): Show |
16 | HG00639.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.293+318delT | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61926033 | |||||||
| chr17:61926095 | C | A | 1 | a0001c0001t0003g0359 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.293+257G>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 2/24 | chr17 | 61926095 | |||||||
| chr17:61927217 | T | C | 1 | a0001c0001t0002g0360 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-19+437A>G | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/24 | chr17 | 61927217 | |||||||
| chr17:61927567 | A | G | 13 | a0001c0001t0005g0003 a0001c0001t0005g0004 a0001c0001t0005g0006 others(10): Show |
13 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+87T>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/24 | chr17 | 61927567 | |||||||
| chr17:61927586 | C | G | 1 | a0001c0001t0007g0002 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+68G>C | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/24 | chr17 | 61927586 | |||||||
| chr17:61927610 | G | A | 1 | a0001c0002t0004g0361 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-19+44C>T | INTS2 | ENSG00000108506.14 | transcript | ENST00000251334.7 | protein_coding | 1/24 | chr17 | 61927610 |