Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3658 |
| ensemblid | ENSG00000136381.13 |
| hgncid | 6115 |
| symbol | IREB2 |
| name | iron responsive element binding protein 2 |
| refseq_nuc | NM_004136.4 |
| refseq_prot | NP_004127.2 |
| ensembl_nuc | ENST00000258886.13 |
| ensembl_prot | ENSP00000258886.8 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 78438216 |
| end | 78501453 |
| strand | + |
| ver | v1.2 |
| region | chr15:78438216-78501453 |
| region5000 | chr15:78433216-78506453 |
| regionname0 | IREB2_chr15_78438216_78501453 |
| regionname5000 | IREB2_chr15_78433216_78506453 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 963 | 405 | 79 | 65 | 204 | 14 | 42 | 162 | IREB2_chr15_78433216_78506453 | IREB2 | MDAPK others(958): Show |
chr15 | 78433216 | 78506453 |
| a0002 | 0/0 | 963 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | MDAPK others(958): Show |
chr15 | 78433216 | 78506453 |
| a0003 | 0/0 | 963 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | MDAPK others(958): Show |
chr15 | 78433216 | 78506453 |
| a0004 | 0/0 | 963 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | MDAPK others(958): Show |
chr15 | 78433216 | 78506453 |
| a0005 | 1/0 | 963 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | MDAPK others(958): Show |
chr15 | 78433216 | 78506453 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2889 | 240 | 52 | 33 | 124 | 6 | 25 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0001c0002 | 0/1 | 2889 | 151 | 22 | 31 | 72 | 8 | 17 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0001c0004 | 0/0 | 2889 | 6 | 0 | 0 | 6 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0001c0006 | 0/0 | 2889 | 4 | 4 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0001c0008 | 0/0 | 2889 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0001c0009 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0001c0012 | 0/0 | 2889 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0002c0003 | 0/0 | 2889 | 7 | 6 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0003c0005 | 0/0 | 2889 | 4 | 4 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0003c0010 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0004c0007 | 0/0 | 2889 | 2 | 0 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 | ||
| a0005c0011 | 1/0 | 2889 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | ATGGA others(2884): Show |
chr15 | 78433216 | 78506453 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6323 | 94 | 9 | 19 | 49 | 3 | 14 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0002 | 0/0 | 6323 | 67 | 12 | 10 | 36 | 2 | 7 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0004 | 0/0 | 6322 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0006 | 0/0 | 6323 | 18 | 16 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0007 | 0/0 | 6322 | 12 | 0 | 0 | 12 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0008 | 0/0 | 6317 | 9 | 0 | 0 | 9 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6312): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0009 | 0/0 | 6322 | 4 | 4 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0011 | 0/0 | 6330 | 5 | 2 | 1 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6325): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0013 | 0/0 | 6322 | 4 | 0 | 0 | 3 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0014 | 0/0 | 6324 | 4 | 0 | 0 | 2 | 0 | 2 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6319): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0016 | 0/0 | 6324 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6319): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0018 | 0/0 | 6322 | 3 | 0 | 0 | 3 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0019 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0020 | 0/0 | 6323 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0021 | 0/0 | 6323 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0029 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0030 | 0/0 | 6322 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0031 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0032 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0033 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6319): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0034 | 0/0 | 6322 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0041 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0043 | 0/0 | 6323 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0045 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0046 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GGGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0047 | 0/0 | 6322 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GGGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0001t0048 | 0/0 | 6325 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GGGCC others(6320): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0003 | 0/0 | 6322 | 57 | 2 | 12 | 37 | 2 | 4 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0004 | 0/0 | 6322 | 39 | 14 | 2 | 19 | 1 | 3 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0005 | 0/1 | 6320 | 32 | 1 | 11 | 7 | 4 | 8 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6315): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0012 | 0/0 | 6321 | 4 | 2 | 1 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6316): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0017 | 0/0 | 6321 | 3 | 0 | 2 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6316): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0022 | 0/0 | 6323 | 2 | 1 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0023 | 0/0 | 6321 | 2 | 0 | 1 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6316): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0026 | 0/0 | 6323 | 2 | 0 | 1 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0027 | 0/0 | 6324 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6319): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0028 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0035 | 0/0 | 6322 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0036 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6319): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0037 | 0/0 | 6322 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0038 | 0/0 | 6322 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0039 | 0/0 | 6323 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0040 | 0/0 | 6322 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0042 | 0/0 | 6322 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0002t0044 | 0/0 | 6322 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0004t0001 | 0/0 | 6323 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0004t0015 | 0/0 | 6323 | 4 | 0 | 0 | 4 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0004t0016 | 0/0 | 6324 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6319): Show |
chr15 | 78433216 | 78506453 |
| a0001c0006t0024 | 0/0 | 6324 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6319): Show |
chr15 | 78433216 | 78506453 |
| a0001c0006t0025 | 0/0 | 6323 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0001c0008t0003 | 0/0 | 6322 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0009t0004 | 0/0 | 6322 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0001c0012t0001 | 0/0 | 6323 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0002c0003t0010 | 0/0 | 6324 | 7 | 6 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6319): Show |
chr15 | 78433216 | 78506453 |
| a0003c0005t0009 | 0/0 | 6322 | 4 | 4 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6317): Show |
chr15 | 78433216 | 78506453 |
| a0003c0010t0001 | 0/0 | 6323 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0004c0007t0019 | 0/0 | 6323 | 2 | 0 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6318): Show |
chr15 | 78433216 | 78506453 |
| a0005c0011t0010 | 1/0 | 6324 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | GAGCC others(6319): Show |
chr15 | 78433216 | 78506453 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 6 | 2 | 0 | 2 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0024 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0002 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0006g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0007g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0008g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0008g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0008g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0008g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0008g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0008g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0008g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0009g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0011g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0011g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0011g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0013g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0013g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0013g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0013g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0014g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0014g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0014g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0014g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0016g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0016g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0018g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0018g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0018g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0019g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0020g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0020g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0021g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0021g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0029g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0030g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0031g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0032g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0033g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0034g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0041g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0043g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0045g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0046g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0047g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0001t0048g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0016 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0003g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0366 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0005g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0012g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0012g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0012g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0012g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0017g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0017g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0017g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0022g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0022g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0023g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0023g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0026g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0026g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0027g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0028g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0035g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0036g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0037g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0038g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0039g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0040g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0042g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0002t0044g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0004t0015g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0004t0015g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0004t0015g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0004t0015g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0004t0016g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0006t0024g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0006t0024g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0006t0025g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0006t0025g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0008t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0008t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0009t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0001c0012t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0002c0003t0010g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0002c0003t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0002c0003t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0002c0003t0010g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0002c0003t0010g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0002c0003t0010g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0003c0005t0009g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0003c0005t0009g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0003c0005t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0003c0005t0009g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0003c0010t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0004c0007t0019g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0004c0007t0019g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| a0005c0011t0010g0299 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00099 | hp2 | a0001 | c0002 | t0005 | g0342 | EUR | GBR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00280 | hp1 | a0001 | c0002 | t0004 | g0269 | EUR | FIN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00280 | hp2 | a0001 | c0002 | t0003 | g0183 | EUR | FIN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00323 | hp1 | a0001 | c0002 | t0017 | g0186 | EUR | FIN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00323 | hp2 | a0001 | c0002 | t0005 | g0370 | EUR | FIN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00408 | hp1 | a0001 | c0002 | t0005 | g0344 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00408 | hp2 | a0001 | c0001 | t0007 | g0321 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0261 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00438 | hp1 | a0001 | c0002 | t0004 | g0160 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00544 | hp1 | a0001 | c0002 | t0003 | g0195 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00558 | hp1 | a0001 | c0002 | t0044 | g0174 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00597 | hp1 | a0001 | c0001 | t0016 | g0059 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0193 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00609 | hp1 | a0001 | c0002 | t0003 | g0167 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00609 | hp2 | a0001 | c0002 | t0005 | g0343 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00639 | hp1 | a0001 | c0002 | t0005 | g0353 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00639 | hp2 | a0001 | c0002 | t0017 | g0176 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0173 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00673 | hp2 | a0001 | c0001 | t0029 | g0029 | EAS | CHS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0179 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00735 | hp2 | a0001 | c0002 | t0003 | g0107 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00738 | hp1 | a0001 | c0002 | t0005 | g0356 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG00741 | hp2 | a0001 | c0002 | t0012 | g0028 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01069 | hp2 | a0001 | c0002 | t0003 | g0191 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01070 | hp2 | a0001 | c0002 | t0042 | g0375 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01081 | hp1 | a0001 | c0002 | t0005 | g0004 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01081 | hp2 | a0001 | c0002 | t0017 | g0180 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01099 | hp1 | a0001 | c0002 | t0005 | g0365 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01099 | hp2 | a0001 | c0012 | t0001 | g0105 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01106 | hp1 | a0001 | c0002 | t0005 | g0004 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0189 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01109 | hp1 | a0002 | c0003 | t0010 | g0013 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0352 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0149 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01169 | hp1 | a0001 | c0002 | t0005 | g0346 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01175 | hp2 | a0001 | c0002 | t0023 | g0349 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01192 | hp1 | a0001 | c0002 | t0005 | g0367 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0190 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01243 | hp2 | a0001 | c0002 | t0004 | g0249 | AMR | PUR | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01255 | hp1 | a0001 | c0002 | t0004 | g0255 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01261 | hp1 | a0004 | c0007 | t0019 | g0293 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01346 | hp1 | a0001 | c0002 | t0005 | g0028 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0002 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01361 | hp1 | a0001 | c0002 | t0005 | g0371 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01496 | hp1 | a0001 | c0001 | t0011 | g0143 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01496 | hp2 | a0004 | c0007 | t0019 | g0292 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0216 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01515 | hp2 | a0001 | c0002 | t0003 | g0016 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01516 | hp2 | a0001 | c0002 | t0005 | g0358 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0217 | EUR | IBS | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01884 | hp1 | a0001 | c0002 | t0012 | g0271 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01884 | hp2 | a0001 | c0002 | t0005 | g0359 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0004 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01891 | hp2 | a0001 | c0002 | t0004 | g0022 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01934 | hp2 | a0001 | c0002 | t0026 | g0204 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01952 | hp2 | a0001 | c0002 | t0003 | g0203 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01975 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02004 | hp1 | a0001 | c0002 | t0003 | g0162 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02004 | hp2 | a0001 | c0001 | t0043 | g0294 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02027 | hp1 | a0001 | c0002 | t0005 | g0368 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02027 | hp2 | a0001 | c0002 | t0012 | g0256 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0109 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02055 | hp2 | a0001 | c0002 | t0004 | g0021 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0172 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02074 | hp1 | a0001 | c0001 | t0007 | g0323 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02080 | hp1 | a0001 | c0002 | t0026 | g0166 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0333 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0192 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0260 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02132 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02135 | hp1 | a0001 | c0001 | t0016 | g0045 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02145 | hp1 | a0002 | c0003 | t0010 | g0138 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0257 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CDX | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0164 | EAS | CDX | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02257 | hp1 | a0002 | c0003 | t0010 | g0141 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02258 | hp2 | a0001 | c0001 | t0034 | g0009 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02280 | hp1 | a0003 | c0010 | t0001 | g0296 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02280 | hp2 | a0001 | c0002 | t0004 | g0248 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0003 | AMR | PEL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0125 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0115 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02615 | hp1 | a0001 | c0001 | t0045 | g0002 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0124 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02630 | hp1 | a0001 | c0006 | t0025 | g0131 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0199 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0341 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02698 | hp2 | a0001 | c0002 | t0005 | g0369 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0113 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0116 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02738 | hp1 | a0001 | c0001 | t0014 | g0056 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02738 | hp2 | a0001 | c0002 | t0003 | g0205 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02818 | hp1 | a0001 | c0002 | t0027 | g0240 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02818 | hp2 | a0001 | c0001 | t0011 | g0142 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02886 | hp1 | a0001 | c0001 | t0047 | g0122 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02886 | hp2 | a0003 | c0005 | t0009 | g0126 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02895 | hp1 | a0001 | c0001 | t0020 | g0135 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02895 | hp2 | a0003 | c0005 | t0009 | g0129 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0111 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02896 | hp2 | a0001 | c0002 | t0004 | g0267 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02897 | hp1 | a0001 | c0001 | t0020 | g0136 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02897 | hp2 | a0001 | c0002 | t0004 | g0251 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0108 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02965 | hp2 | a0003 | c0005 | t0009 | g0127 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0259 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02976 | hp1 | a0001 | c0006 | t0024 | g0133 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03041 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0275 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0121 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03130 | hp1 | a0001 | c0006 | t0024 | g0134 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03139 | hp1 | a0003 | c0005 | t0009 | g0128 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03139 | hp2 | a0001 | c0006 | t0025 | g0132 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03195 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03209 | hp1 | a0002 | c0003 | t0010 | g0140 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03209 | hp2 | a0001 | c0001 | t0009 | g0012 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0266 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03453 | hp1 | a0001 | c0001 | t0031 | g0008 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0145 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03486 | hp2 | a0002 | c0003 | t0010 | g0137 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03491 | hp1 | a0001 | c0002 | t0040 | g0201 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03491 | hp2 | a0001 | c0002 | t0004 | g0023 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03492 | hp2 | a0001 | c0002 | t0004 | g0023 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03540 | hp1 | a0001 | c0009 | t0004 | g0022 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03654 | hp2 | a0001 | c0002 | t0005 | g0364 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03704 | hp2 | a0001 | c0002 | t0005 | g0347 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03710 | hp1 | a0001 | c0002 | t0005 | g0354 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0188 | SAS | PJL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0104 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03834 | hp1 | a0001 | c0001 | t0013 | g0331 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03834 | hp2 | a0001 | c0002 | t0003 | g0312 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03942 | hp2 | a0001 | c0002 | t0039 | g0202 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG04115 | hp2 | a0001 | c0002 | t0005 | g0357 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG04184 | hp1 | a0001 | c0002 | t0005 | g0355 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG04184 | hp2 | a0001 | c0001 | t0014 | g0064 | SAS | BEB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG04199 | hp1 | a0001 | c0002 | t0005 | g0363 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG04228 | hp1 | a0001 | c0002 | t0004 | g0264 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | STU | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18612 | hp1 | a0001 | c0002 | t0005 | g0348 | EAS | CHB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18612 | hp2 | a0001 | c0002 | t0003 | g0187 | EAS | CHB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0178 | EAS | CHB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0270 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18939 | hp1 | a0001 | c0001 | t0007 | g0324 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18941 | hp1 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18942 | hp1 | a0001 | c0002 | t0035 | g0021 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18942 | hp2 | a0001 | c0001 | t0008 | g0320 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18943 | hp1 | a0001 | c0001 | t0007 | g0322 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18943 | hp2 | a0001 | c0001 | t0014 | g0034 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18944 | hp1 | a0001 | c0002 | t0004 | g0019 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18947 | hp1 | a0001 | c0001 | t0013 | g0328 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18948 | hp2 | a0001 | c0008 | t0003 | g0182 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18949 | hp1 | a0001 | c0002 | t0028 | g0242 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18950 | hp1 | a0001 | c0001 | t0014 | g0087 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18950 | hp2 | a0001 | c0002 | t0003 | g0158 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18951 | hp2 | a0001 | c0002 | t0004 | g0262 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18952 | hp1 | a0001 | c0001 | t0018 | g0326 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18954 | hp2 | a0001 | c0002 | t0038 | g0165 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18956 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18957 | hp1 | a0001 | c0008 | t0003 | g0181 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18960 | hp1 | a0001 | c0001 | t0007 | g0335 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18962 | hp1 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0197 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18968 | hp1 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0241 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18969 | hp2 | a0001 | c0002 | t0004 | g0273 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18970 | hp2 | a0001 | c0002 | t0003 | g0159 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18972 | hp1 | a0001 | c0001 | t0013 | g0330 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18972 | hp2 | a0001 | c0001 | t0008 | g0316 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18975 | hp1 | a0001 | c0001 | t0008 | g0314 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18975 | hp2 | a0001 | c0001 | t0011 | g0146 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18977 | hp2 | a0001 | c0001 | t0018 | g0327 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18978 | hp1 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18978 | hp2 | a0001 | c0004 | t0015 | g0100 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18980 | hp1 | a0001 | c0002 | t0004 | g0245 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18981 | hp2 | a0001 | c0002 | t0005 | g0362 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18982 | hp1 | a0001 | c0004 | t0015 | g0040 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18983 | hp1 | a0001 | c0002 | t0004 | g0268 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18983 | hp2 | a0001 | c0001 | t0007 | g0334 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18989 | hp1 | a0001 | c0001 | t0021 | g0337 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0171 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18990 | hp1 | a0001 | c0002 | t0004 | g0244 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18991 | hp1 | a0001 | c0001 | t0008 | g0319 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18992 | hp2 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18997 | hp1 | a0001 | c0004 | t0001 | g0094 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0157 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18999 | hp1 | a0001 | c0002 | t0004 | g0246 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA18999 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19003 | hp1 | a0001 | c0001 | t0030 | g0073 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19005 | hp1 | a0001 | c0001 | t0018 | g0325 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19005 | hp2 | a0001 | c0001 | t0041 | g0185 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19007 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19007 | hp2 | a0001 | c0002 | t0004 | g0253 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19009 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19009 | hp2 | a0001 | c0002 | t0004 | g0243 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19012 | hp1 | a0001 | c0002 | t0004 | g0254 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19012 | hp2 | a0001 | c0001 | t0008 | g0315 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19030 | hp1 | a0001 | c0002 | t0004 | g0258 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19030 | hp2 | a0001 | c0001 | t0048 | g0123 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0250 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0339 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19054 | hp2 | a0001 | c0004 | t0016 | g0095 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19055 | hp1 | a0001 | c0002 | t0005 | g0361 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0239 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19057 | hp2 | a0001 | c0001 | t0011 | g0144 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19058 | hp2 | a0001 | c0002 | t0004 | g0019 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19064 | hp1 | a0001 | c0001 | t0007 | g0332 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19066 | hp1 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19067 | hp1 | a0001 | c0001 | t0008 | g0317 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19067 | hp2 | a0001 | c0002 | t0036 | g0263 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19068 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19072 | hp2 | a0001 | c0002 | t0003 | g0340 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19074 | hp1 | a0001 | c0002 | t0004 | g0200 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19076 | hp1 | a0001 | c0001 | t0032 | g0036 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19076 | hp2 | a0001 | c0002 | t0023 | g0360 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19078 | hp1 | a0001 | c0002 | t0022 | g0265 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19079 | hp1 | a0001 | c0002 | t0004 | g0272 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19079 | hp2 | a0001 | c0001 | t0008 | g0318 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19081 | hp2 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19082 | hp1 | a0001 | c0004 | t0015 | g0101 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19082 | hp2 | a0001 | c0002 | t0003 | g0175 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19083 | hp1 | a0001 | c0004 | t0015 | g0099 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0338 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19085 | hp2 | a0001 | c0001 | t0007 | g0336 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0161 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19087 | hp2 | a0001 | c0001 | t0021 | g0027 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19088 | hp2 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19090 | hp2 | a0001 | c0001 | t0013 | g0329 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19091 | hp1 | a0001 | c0002 | t0005 | g0345 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0002 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA19240 | hp2 | a0002 | c0003 | t0010 | g0139 | AFR | YRI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ASW | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0252 | AFR | ASW | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA20805 | hp1 | a0001 | c0001 | t0019 | g0291 | EUR | TSI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA20805 | hp2 | a0001 | c0002 | t0005 | g0004 | EUR | TSI | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA20905 | hp2 | a0001 | c0002 | t0005 | g0372 | SAS | GIH | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01123 | hp1 | a0001 | c0002 | t0005 | g0350 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0184 | AMR | CLM | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02109 | hp2 | a0001 | c0001 | t0033 | g0130 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02486 | hp1 | a0001 | c0002 | t0022 | g0247 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02486 | hp2 | a0001 | c0002 | t0037 | g0351 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0155 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0376 | AFR | ACB | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | MSL | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | USA | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | USA | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA20300 | hp1 | a0001 | c0002 | t0012 | g0274 | AFR | USA | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA20300 | hp2 | a0002 | c0003 | t0010 | g0013 | AFR | USA | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA21309 | hp1 | a0001 | c0001 | t0046 | g0117 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| NA21309 | hp2 | a0001 | c0002 | t0003 | g0374 | AFR | LWK | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0005 | g0366 | REF | REF | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| homoSapiens | grch38p0 | a0005 | c0011 | t0010 | g0299 | REF | REF | IREB2_chr15_78433216_78506453 | IREB2 | chr15 | 78433216 | 78506453 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:78466335 | C | G | 1 | a0002 | 7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
missense_variant | MODERATE | c.475C>G | p.Leu159Val | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/22 | 597/6324 | 475/2892 | 159/963 | chr15 | 78466335 | |||
| chr15:78487762 | T | C | 3 | a0001 a0003 a0004 |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
missense_variant | MODERATE | c.1739T>C | p.Ile580Thr | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 14/22 | 1861/6324 | 1739/2892 | 580/963 | chr15 | 78487762 | |||
| chr15:78490631 | A | G | 1 | a0003 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.2194A>G | p.Ile732Val | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/22 | 2316/6324 | 2194/2892 | 732/963 | chr15 | 78490631 | |||
| chr15:78490631 | A | T | 1 | a0003 | 4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.2194A>T | p.Ile732Phe | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/22 | 2316/6324 | 2194/2892 | 732/963 | chr15 | 78490631 | |||
| chr15:78497192 | A | G | 1 | a0004 | 2 | HG01261.hp1 HG01496.hp2 |
missense_variant | MODERATE | c.2662A>G | p.Ile888Val | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/22 | 2784/6324 | 2662/2892 | 888/963 | chr15 | 78497192 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:78471825 | A | C | 1 | a0001c0008 | 2 | NA18948.hp2 NA18957.hp1 |
synonymous_variant | LOW | c.784A>C | p.Arg262Arg | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/22 | 906/6324 | 784/2892 | 262/963 | chr15 | 78471825 | |||
| chr15:78471845 | A | G | 1 | a0001c0006 | 4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.804A>G | p.Lys268Lys | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/22 | 926/6324 | 804/2892 | 268/963 | chr15 | 78471845 | |||
| chr15:78478316 | C | T | 1 | a0001c0012 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.1215C>T | p.Leu405Leu | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/22 | 1337/6324 | 1215/2892 | 405/963 | chr15 | 78478316 | |||
| chr15:78484844 | G | A | 1 | a0001c0004 | 6 | NA18978.hp2 NA18982.hp1 NA18997.hp1 others(3): Show |
synonymous_variant | LOW | c.1497G>A | p.Leu499Leu | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/22 | 1619/6324 | 1497/2892 | 499/963 | chr15 | 78484844 | |||
| chr15:78497146 | C | T | 3 | a0001c0002 a0001c0008 a0001c0009 |
153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
synonymous_variant | LOW | c.2616C>T | p.Ala872Ala | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/22 | 2738/6324 | 2616/2892 | 872/963 | chr15 | 78497146 | |||
| chr15:78497299 | A | C | 1 | a0001c0009 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.2769A>C | p.Thr923Thr | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/22 | 2891/6324 | 2769/2892 | 923/963 | chr15 | 78497299 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:78438217 | A | G | 3 | a0001c0001t0046 a0001c0001t0047 a0001c0001t0048 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-121A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/22 | 121 | chr15 | 78438217 | ||||||
| chr15:78438227 | C | T | 1 | a0001c0001t0045 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-111C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/22 | 111 | chr15 | 78438227 | ||||||
| chr15:78438249 | C | T | 15 | a0001c0001t0002 a0001c0001t0018 a0001c0001t0019 others(12): Show |
144 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(141): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-89C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/22 | chr15 | 78438249 | |||||||
| chr15:78438265 | C | A | 1 | a0001c0002t0038 | 1 | NA18954.hp2 | 5_prime_UTR_variant | MODIFIER | c.-73C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/22 | 73 | chr15 | 78438265 | ||||||
| chr15:78438330 | C | T | 1 | a0001c0004t0015 | 4 | NA18978.hp2 NA18982.hp1 NA19082.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-8C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/22 | 8 | chr15 | 78438330 | ||||||
| chr15:78498393 | TG | T | 44 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(41): Show |
325 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(322): Show |
3_prime_UTR_variant | MODIFIER | c.*260delG | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 260 | INFO_REALIGN_3_PRIME | chr15 | 78498393 | |||||
| chr15:78498394 | G | T | 1 | a0001c0001t0002 | 2 | HG02074.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*251G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 251 | chr15 | 78498394 | ||||||
| chr15:78498397 | G | T | 1 | a0001c0002t0044 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 254 | chr15 | 78498397 | ||||||
| chr15:78498430 | A | G | 1 | a0001c0002t0035 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 287 | chr15 | 78498430 | ||||||
| chr15:78498499 | A | G | 6 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0013 others(3): Show |
29 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*356A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 356 | chr15 | 78498499 | ||||||
| chr15:78498708 | G | A | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(50): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
3_prime_UTR_variant | MODIFIER | c.*565G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 565 | chr15 | 78498708 | ||||||
| chr15:78498719 | C | T | 4 | a0001c0001t0002 a0001c0001t0019 a0001c0001t0043 others(1): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*576C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 576 | chr15 | 78498719 | ||||||
| chr15:78499225 | A | G | 1 | a0001c0001t0033 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1082A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1082 | chr15 | 78499225 | ||||||
| chr15:78499390 | G | A | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(50): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
3_prime_UTR_variant | MODIFIER | c.*1247G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1247 | chr15 | 78499390 | ||||||
| chr15:78499509 | G | A | 3 | a0001c0001t0046 a0001c0001t0047 a0001c0001t0048 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1366G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1366 | chr15 | 78499509 | ||||||
| chr15:78499569 | A | G | 1 | a0001c0001t0043 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1426A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1426 | chr15 | 78499569 | ||||||
| chr15:78499658 | G | A | 3 | a0001c0001t0006 a0001c0001t0034 a0001c0001t0045 |
20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1515G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1515 | chr15 | 78499658 | ||||||
| chr15:78499679 | C | G | 1 | a0001c0001t0045 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1536C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1536 | chr15 | 78499679 | ||||||
| chr15:78499757 | A | G | 1 | a0001c0001t0032 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1614A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1614 | chr15 | 78499757 | ||||||
| chr15:78499876 | C | T | 1 | a0001c0001t0020 | 2 | HG02895.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1733C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1733 | chr15 | 78499876 | ||||||
| chr15:78499909 | A | G | 1 | a0001c0002t0042 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1766A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1766 | chr15 | 78499909 | ||||||
| chr15:78500056 | T | C | 21 | a0001c0001t0004 a0001c0002t0003 a0001c0002t0004 others(18): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*1913T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1913 | chr15 | 78500056 | ||||||
| chr15:78500097 | G | A | 13 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0016 others(10): Show |
113 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1954G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 1954 | chr15 | 78500097 | ||||||
| chr15:78500145 | C | T | 1 | a0001c0001t0011 | 5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2002C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2002 | chr15 | 78500145 | ||||||
| chr15:78500185 | T | C | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0014 others(19): Show |
192 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*2042T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2042 | chr15 | 78500185 | ||||||
| chr15:78500186 | G | T | 2 | a0001c0001t0019 a0004c0007t0019 |
3 | HG01261.hp1 HG01496.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2043G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2043 | chr15 | 78500186 | ||||||
| chr15:78500355 | A | G | 2 | a0001c0002t0039 a0001c0002t0040 |
2 | HG03491.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2212A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2212 | chr15 | 78500355 | ||||||
| chr15:78500538 | C | CA | 5 | a0001c0001t0016 a0001c0001t0033 a0001c0001t0048 others(2): Show |
6 | HG00597.hp1 HG02109.hp2 HG02135.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2414dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2415 | INFO_REALIGN_3_PRIME | chr15 | 78500538 | |||||
| chr15:78500538 | CA | C | 25 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(22): Show |
215 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*2414delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2414 | INFO_REALIGN_3_PRIME | chr15 | 78500538 | |||||
| chr15:78500538 | CAA | C | 3 | a0001c0002t0012 a0001c0002t0017 a0001c0002t0037 |
8 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2413_*2414delAA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2413 | INFO_REALIGN_3_PRIME | chr15 | 78500538 | |||||
| chr15:78500538 | CAAA | C | 2 | a0001c0002t0005 a0001c0002t0023 |
33 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2412_*2414delAAA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2412 | INFO_REALIGN_3_PRIME | chr15 | 78500538 | |||||
| chr15:78500538 | CAAAAAA | C | 1 | a0001c0001t0008 | 9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2409_*2414delAAAA others(2): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2409 | INFO_REALIGN_3_PRIME | chr15 | 78500538 | |||||
| chr15:78500552 | A | G | 4 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0018 others(1): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2409A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2409 | chr15 | 78500552 | ||||||
| chr15:78500561 | A | AGTGTAAT others(1): Show |
1 | a0001c0001t0011 | 5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2419_*2426dupGTGT others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2427 | INFO_REALIGN_3_PRIME | chr15 | 78500561 | |||||
| chr15:78500629 | C | T | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(50): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
3_prime_UTR_variant | MODIFIER | c.*2486C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2486 | chr15 | 78500629 | ||||||
| chr15:78500659 | G | A | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(53): Show |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
3_prime_UTR_variant | MODIFIER | c.*2516G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2516 | chr15 | 78500659 | ||||||
| chr15:78500673 | A | G | 1 | a0001c0001t0013 | 4 | HG03834.hp1 NA18947.hp1 NA18972.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2530A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2530 | chr15 | 78500673 | ||||||
| chr15:78500743 | C | A | 4 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0018 others(1): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2600C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2600 | chr15 | 78500743 | ||||||
| chr15:78500745 | A | T | 1 | a0001c0001t0029 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2602A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2602 | chr15 | 78500745 | ||||||
| chr15:78500767 | T | C | 4 | a0001c0001t0002 a0001c0001t0019 a0001c0001t0043 others(1): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2624T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 22/22 | 2624 | chr15 | 78500767 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:78438627 | C | G | 1 | a0001c0001t0006g0376 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.19+271C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438627 | |||||||
| chr15:78438656 | C | T | 1 | a0001c0002t0042g0375 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.19+300C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438656 | |||||||
| chr15:78438679 | G | A | 1 | a0001c0001t0029g0029 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.19+323G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438679 | |||||||
| chr15:78438709 | C | G | 1 | a0001c0002t0003g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.19+353C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438709 | |||||||
| chr15:78438753 | C | T | 1 | a0001c0001t0001g0373 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.19+397C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438753 | |||||||
| chr15:78438807 | C | T | 34 | a0001c0002t0004g0004 a0001c0002t0005g0004 a0001c0002t0005g0028 others(31): Show |
36 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.19+451C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438807 | |||||||
| chr15:78438853 | A | T | 1 | a0001c0001t0001g0341 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.19+497A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438853 | |||||||
| chr15:78438918 | C | CA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(83): Show |
98 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.19+575dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr15 | 78438918 | ||||||
| chr15:78438918 | CA | C | 22 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(19): Show |
22 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.19+575delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr15 | 78438918 | ||||||
| chr15:78438946 | A | G | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+590A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78438946 | |||||||
| chr15:78439095 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.20-700C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439095 | |||||||
| chr15:78439233 | C | T | 2 | a0001c0002t0003g0107 a0001c0002t0003g0312 |
2 | HG00735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.20-562C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439233 | |||||||
| chr15:78439398 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.20-397C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439398 | |||||||
| chr15:78439419 | C | T | 1 | a0001c0012t0001g0105 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.20-376C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439419 | |||||||
| chr15:78439466 | T | A | 280 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(277): Show |
304 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.20-329T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439466 | |||||||
| chr15:78439668 | A | G | 21 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0276 others(18): Show |
23 | HG01074.hp2 HG01255.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.20-127A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 1/21 | chr15 | 78439668 | |||||||
| chr15:78440168 | G | A | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.106+287G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440168 | |||||||
| chr15:78440191 | T | C | 16 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(13): Show |
20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+310T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440191 | |||||||
| chr15:78440370 | C | CT | 136 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(133): Show |
149 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.106+500dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78440370 | ||||||
| chr15:78440412 | A | G | 281 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(278): Show |
305 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.106+531A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440412 | |||||||
| chr15:78440533 | A | G | 3 | a0001c0002t0005g0369 a0001c0002t0005g0370 a0001c0002t0005g0371 |
3 | HG00323.hp2 HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.106+652A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440533 | |||||||
| chr15:78440555 | T | C | 1 | a0001c0001t0046g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.106+674T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440555 | |||||||
| chr15:78440736 | A | G | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+855A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440736 | |||||||
| chr15:78440798 | C | A | 1 | a0001c0001t0002g0276 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.106+917C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78440798 | |||||||
| chr15:78441048 | A | T | 77 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(74): Show |
82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.106+1167A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441048 | |||||||
| chr15:78441239 | AAC | A | 36 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0030 others(33): Show |
38 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.106+1360_106+1361d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78441239 | ||||||
| chr15:78441389 | T | C | 77 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(74): Show |
82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.106+1508T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441389 | |||||||
| chr15:78441474 | T | C | 1 | a0001c0002t0027g0240 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.106+1593T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441474 | |||||||
| chr15:78441514 | ATAAAT | A | 8 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0241 others(5): Show |
10 | NA18944.hp1 NA18949.hp1 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.106+1638_106+1642d others(7): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78441514 | ||||||
| chr15:78441712 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
6 | HG00423.hp2 HG02056.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+1831G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441712 | |||||||
| chr15:78441916 | T | C | 4 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+2035T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441916 | |||||||
| chr15:78441950 | A | G | 132 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(129): Show |
144 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.106+2069A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441950 | |||||||
| chr15:78441954 | T | C | 1 | a0001c0002t0005g0342 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.106+2073T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441954 | |||||||
| chr15:78441980 | C | A | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+2099C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441980 | |||||||
| chr15:78441997 | C | G | 21 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(18): Show |
25 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.106+2116C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78441997 | |||||||
| chr15:78442243 | A | G | 77 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(74): Show |
82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.106+2362A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442243 | |||||||
| chr15:78442246 | ATTAC | A | 77 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(74): Show |
82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.106+2369_106+2372d others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78442246 | ||||||
| chr15:78442415 | G | T | 1 | a0001c0002t0003g0206 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.106+2534G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442415 | |||||||
| chr15:78442463 | C | T | 1 | a0001c0002t0005g0368 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.106+2582C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442463 | |||||||
| chr15:78442491 | T | A | 1 | a0001c0001t0001g0295 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.106+2610T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442491 | |||||||
| chr15:78442546 | C | T | 1 | a0001c0001t0043g0294 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.106+2665C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442546 | |||||||
| chr15:78442582 | T | C | 1 | a0001c0001t0007g0321 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.106+2701T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442582 | |||||||
| chr15:78442667 | C | G | 378 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(375): Show |
414 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(411): Show |
intron_variant | MODIFIER | c.106+2786C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442667 | |||||||
| chr15:78442728 | A | C | 132 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(129): Show |
144 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.106+2847A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442728 | |||||||
| chr15:78442758 | C | T | 6 | a0002c0003t0010g0013 a0002c0003t0010g0137 a0002c0003t0010g0138 others(3): Show |
7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+2877C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442758 | |||||||
| chr15:78442808 | A | C | 1 | a0001c0002t0004g0275 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.106+2927A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442808 | |||||||
| chr15:78442816 | T | C | 3 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0022g0247 |
3 | HG01243.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.106+2935T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442816 | |||||||
| chr15:78442927 | C | T | 77 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(74): Show |
82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.106+3046C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78442927 | |||||||
| chr15:78443013 | C | G | 132 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(129): Show |
144 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.106+3132C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443013 | |||||||
| chr15:78443096 | G | C | 77 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(74): Show |
82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.106+3215G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443096 | |||||||
| chr15:78443194 | G | A | 1 | a0002c0003t0010g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.106+3313G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443194 | |||||||
| chr15:78443384 | G | A | 11 | a0001c0001t0007g0322 a0001c0001t0007g0323 a0001c0001t0007g0324 others(8): Show |
11 | HG02074.hp1 HG03834.hp1 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+3503G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443384 | |||||||
| chr15:78443532 | T | C | 3 | a0001c0001t0046g0117 a0001c0001t0047g0122 a0001c0001t0048g0123 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.106+3651T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443532 | |||||||
| chr15:78443534 | T | C | 1 | a0001c0002t0004g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.106+3653T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443534 | |||||||
| chr15:78443626 | G | T | 1 | a0001c0002t0003g0205 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.106+3745G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443626 | |||||||
| chr15:78443657 | G | T | 1 | a0001c0001t0001g0311 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.106+3776G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443657 | |||||||
| chr15:78443842 | C | T | 61 | a0001c0001t0041g0185 a0001c0002t0003g0003 a0001c0002t0003g0006 others(58): Show |
69 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.106+3961C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443842 | |||||||
| chr15:78443983 | G | A | 61 | a0001c0001t0041g0185 a0001c0002t0003g0003 a0001c0002t0003g0006 others(58): Show |
69 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.106+4102G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78443983 | |||||||
| chr15:78444080 | G | A | 1 | a0001c0001t0007g0333 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.106+4199G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78444080 | |||||||
| chr15:78444251 | T | A | 280 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(277): Show |
304 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.106+4370T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78444251 | |||||||
| chr15:78444523 | C | G | 1 | a0001c0001t0008g0320 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.106+4642C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78444523 | |||||||
| chr15:78444665 | T | C | 380 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(377): Show |
416 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(413): Show |
intron_variant | MODIFIER | c.106+4784T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78444665 | |||||||
| chr15:78445136 | AT | A | 8 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(5): Show |
8 | HG01070.hp1 HG02735.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+5274delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78445136 | ||||||
| chr15:78445136 | ATT | A | 18 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(15): Show |
18 | HG00408.hp2 HG01243.hp2 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.106+5273_106+5274d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78445136 | ||||||
| chr15:78445138 | T | TTTA | 63 | a0001c0001t0004g0104 a0001c0001t0041g0185 a0001c0002t0003g0003 others(60): Show |
71 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.106+5259_106+5260i others(5): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78445138 | ||||||
| chr15:78445139 | T | TA | 4 | a0003c0005t0009g0126 a0003c0005t0009g0127 a0003c0005t0009g0128 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+5258_106+5259i others(3): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445139 | |||||||
| chr15:78445140 | T | A | 4 | a0001c0001t0001g0035 a0001c0001t0009g0012 a0001c0001t0009g0124 others(1): Show |
5 | HG00099.hp1 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.106+5259T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445140 | |||||||
| chr15:78445140 | T | TA | 5 | a0001c0002t0005g0367 a0001c0006t0024g0133 a0001c0006t0024g0134 others(2): Show |
5 | HG01192.hp1 HG02630.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+5259_106+5260i others(3): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445140 | |||||||
| chr15:78445141 | T | A | 104 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(101): Show |
115 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.106+5260T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445141 | |||||||
| chr15:78445141 | T | TA | 3 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0043g0294 |
3 | HG01978.hp2 HG02004.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.106+5260_106+5261i others(3): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445141 | |||||||
| chr15:78445142 | T | A | 68 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(65): Show |
72 | HG00438.hp1 HG00738.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.106+5261T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445142 | |||||||
| chr15:78445143 | T | A | 1 | a0001c0002t0003g0162 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.106+5262T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445143 | |||||||
| chr15:78445146 | T | A | 43 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(40): Show |
46 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.106+5265T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445146 | |||||||
| chr15:78445319 | G | C | 1 | a0001c0001t0001g0295 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.106+5438G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445319 | |||||||
| chr15:78445485 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.106+5604A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445485 | |||||||
| chr15:78445495 | A | G | 1 | a0001c0001t0002g0288 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.106+5614A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445495 | |||||||
| chr15:78445600 | G | T | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+5719G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445600 | |||||||
| chr15:78445932 | A | T | 1 | a0001c0001t0033g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.106+6051A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78445932 | |||||||
| chr15:78446028 | T | C | 277 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(274): Show |
301 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.106+6147T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446028 | |||||||
| chr15:78446079 | C | T | 6 | a0002c0003t0010g0013 a0002c0003t0010g0137 a0002c0003t0010g0138 others(3): Show |
7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+6198C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446079 | |||||||
| chr15:78446293 | A | G | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+6412A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446293 | |||||||
| chr15:78446438 | C | T | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.106+6557C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446438 | |||||||
| chr15:78446716 | C | A | 1 | a0001c0001t0009g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.106+6835C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446716 | |||||||
| chr15:78446778 | G | A | 15 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(12): Show |
17 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.106+6897G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78446778 | |||||||
| chr15:78446891 | C | CAGT | 282 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(279): Show |
306 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(303): Show |
intron_variant | MODIFIER | c.106+7011_106+7013d others(5): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78446891 | ||||||
| chr15:78447129 | T | C | 281 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(278): Show |
305 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.106+7248T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447129 | |||||||
| chr15:78447167 | TTTTC | T | 3 | a0001c0002t0003g0003 a0001c0002t0003g0203 a0001c0002t0026g0204 |
6 | HG01928.hp2 HG01934.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.106+7298_106+7301d others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447167 | ||||||
| chr15:78447179 | C | CT | 15 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0096 others(12): Show |
15 | HG00438.hp2 HG01167.hp1 NA18952.hp1 others(12): Show |
intron_variant | MODIFIER | c.106+7313dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447179 | ||||||
| chr15:78447179 | CT | C | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0002g0207 others(4): Show |
7 | NA18941.hp1 NA18959.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+7313delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447179 | ||||||
| chr15:78447320 | T | A | 1 | a0001c0001t0002g0276 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.106+7439T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447320 | |||||||
| chr15:78447332 | A | AT | 108 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0311 others(105): Show |
120 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+7467dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447332 | ||||||
| chr15:78447332 | A | ATT | 34 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0030 others(31): Show |
36 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.106+7466_106+7467d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447332 | ||||||
| chr15:78447332 | AT | A | 6 | a0001c0001t0001g0043 a0001c0001t0001g0301 a0001c0001t0047g0122 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+7467delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447332 | ||||||
| chr15:78447421 | A | G | 33 | a0001c0002t0004g0004 a0001c0002t0005g0004 a0001c0002t0005g0028 others(30): Show |
35 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.106+7540A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447421 | |||||||
| chr15:78447523 | A | G | 4 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+7642A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447523 | |||||||
| chr15:78447524 | T | C | 1 | a0001c0002t0022g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.106+7643T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447524 | |||||||
| chr15:78447538 | C | G | 5 | a0002c0003t0010g0013 a0002c0003t0010g0137 a0002c0003t0010g0139 others(2): Show |
6 | HG01109.hp1 HG02257.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.106+7657C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447538 | |||||||
| chr15:78447592 | A | G | 1 | a0001c0002t0004g0273 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.106+7711A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447592 | |||||||
| chr15:78447617 | C | T | 1 | a0001c0002t0004g0272 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.106+7736C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447617 | |||||||
| chr15:78447626 | C | T | 3 | a0001c0001t0001g0297 a0001c0002t0039g0202 a0001c0002t0040g0201 |
3 | HG02723.hp2 HG03491.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.106+7745C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447626 | |||||||
| chr15:78447709 | C | A | 2 | a0001c0006t0025g0131 a0001c0006t0025g0132 |
2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.106+7828C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447709 | |||||||
| chr15:78447775 | T | C | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.106+7894T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447775 | |||||||
| chr15:78447780 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.106+7899C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447780 | |||||||
| chr15:78447827 | A | AGGTATCA others(19): Show |
1 | a0001c0002t0004g0273 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.106+7947_106+7972d others(28): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78447827 | ||||||
| chr15:78447891 | G | A | 275 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(272): Show |
299 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.106+8010G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447891 | |||||||
| chr15:78447908 | G | C | 1 | a0001c0002t0003g0164 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.106+8027G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78447908 | |||||||
| chr15:78448126 | AATGTATG others(1): Show |
A | 3 | a0001c0001t0046g0117 a0001c0001t0047g0122 a0001c0001t0048g0123 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.106+8260_106+8267d others(10): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78448126 | ||||||
| chr15:78448184 | A | G | 16 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(13): Show |
20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.106+8303A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448184 | |||||||
| chr15:78448293 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.106+8412C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448293 | |||||||
| chr15:78448296 | C | T | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.106+8415C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448296 | |||||||
| chr15:78448306 | G | T | 1 | a0001c0001t0002g0237 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.106+8425G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448306 | |||||||
| chr15:78448346 | T | G | 110 | a0001c0001t0001g0044 a0001c0001t0006g0002 a0001c0001t0006g0009 others(107): Show |
121 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.106+8465T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448346 | |||||||
| chr15:78448369 | T | C | 22 | a0001c0002t0003g0006 a0001c0002t0003g0014 a0001c0002t0003g0015 others(19): Show |
26 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.106+8488T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448369 | |||||||
| chr15:78448437 | G | A | 3 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0022g0247 |
3 | HG01243.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.106+8556G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448437 | |||||||
| chr15:78448590 | A | C | 109 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(106): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.106+8709A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448590 | |||||||
| chr15:78448622 | G | A | 109 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(106): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.106+8741G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448622 | |||||||
| chr15:78448692 | C | T | 2 | a0001c0002t0004g0160 a0001c0002t0004g0200 |
2 | HG00438.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.106+8811C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78448692 | |||||||
| chr15:78449003 | C | A | 34 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0030 others(31): Show |
36 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.106+9122C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449003 | |||||||
| chr15:78449040 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.106+9159G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449040 | |||||||
| chr15:78449042 | T | C | 277 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(274): Show |
301 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.106+9161T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449042 | |||||||
| chr15:78449043 | G | A | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+9162G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449043 | |||||||
| chr15:78449230 | T | C | 2 | a0001c0002t0003g0238 a0001c0002t0003g0239 |
2 | NA18962.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.106+9349T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449230 | |||||||
| chr15:78449276 | T | C | 76 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(73): Show |
81 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.106+9395T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449276 | |||||||
| chr15:78449290 | G | T | 3 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0022g0247 |
3 | HG01243.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.106+9409G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449290 | |||||||
| chr15:78449550 | C | G | 2 | a0001c0001t0002g0149 a0001c0001t0002g0154 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.106+9669C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449550 | |||||||
| chr15:78449773 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.106+9892C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449773 | |||||||
| chr15:78449787 | A | G | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+9906A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449787 | |||||||
| chr15:78449834 | T | C | 3 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 |
4 | NA18968.hp1 NA18975.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+9953T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449834 | |||||||
| chr15:78449902 | G | A | 5 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG00558.hp2 HG02015.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+10021G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449902 | |||||||
| chr15:78449904 | A | G | 1 | a0001c0001t0002g0236 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.106+10023A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449904 | |||||||
| chr15:78449933 | A | G | 1 | a0001c0001t0001g0313 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.106+10052A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449933 | |||||||
| chr15:78449934 | T | G | 276 | a0001c0001t0001g0044 a0001c0001t0002g0017 a0001c0001t0002g0018 others(273): Show |
300 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.106+10053T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78449934 | |||||||
| chr15:78450034 | G | A | 76 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(73): Show |
81 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.106+10153G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450034 | |||||||
| chr15:78450048 | T | A | 1 | a0001c0001t0016g0045 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.106+10167T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450048 | |||||||
| chr15:78450237 | A | G | 76 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(73): Show |
81 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.106+10356A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450237 | |||||||
| chr15:78450412 | C | A | 131 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(128): Show |
143 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.106+10531C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450412 | |||||||
| chr15:78450596 | G | A | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.106+10715G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450596 | |||||||
| chr15:78450687 | G | A | 275 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(272): Show |
299 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.106+10806G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450687 | |||||||
| chr15:78450707 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.106+10826C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450707 | |||||||
| chr15:78450824 | T | TTG | 34 | a0001c0001t0001g0086 a0001c0001t0001g0102 a0001c0001t0001g0297 others(31): Show |
36 | HG00544.hp1 HG00558.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.106+10991_106+1099 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | T | TTGTG | 14 | a0001c0001t0001g0088 a0001c0001t0001g0306 a0001c0001t0006g0010 others(11): Show |
17 | HG00438.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.106+10989_106+1099 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | T | TTGTGTG | 3 | a0001c0001t0006g0116 a0001c0002t0003g0159 a0001c0002t0003g0161 |
3 | HG02723.hp1 NA18970.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.106+10987_106+1099 others(10): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | TTG | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(76): Show |
94 | HG00280.hp2 HG00609.hp1 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.106+10991_106+1099 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | TTGTG | T | 70 | a0001c0001t0001g0035 a0001c0001t0001g0052 a0001c0001t0001g0053 others(67): Show |
74 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.106+10989_106+1099 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | TTGTGTG | T | 47 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0002g0017 others(44): Show |
50 | HG00280.hp1 HG00609.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.106+10987_106+1099 others(10): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | TTGTGTGT others(1): Show |
T | 54 | a0001c0001t0001g0049 a0001c0001t0002g0024 a0001c0001t0002g0025 others(51): Show |
58 | HG00423.hp1 HG00639.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.106+10985_106+1099 others(12): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | TTGTGTGT others(3): Show |
T | 9 | a0001c0001t0001g0048 a0001c0001t0002g0212 a0001c0001t0002g0213 others(6): Show |
9 | HG01175.hp2 HG01257.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+10983_106+1099 others(14): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | TTGTGTGT others(5): Show |
T | 3 | a0001c0002t0004g0249 a0001c0002t0004g0250 a0001c0002t0004g0252 |
3 | HG01243.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.106+10981_106+1099 others(16): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | TTGTGTGT others(7): Show |
T | 3 | a0001c0002t0004g0248 a0001c0002t0005g0346 a0001c0002t0005g0347 |
3 | HG01169.hp1 HG02280.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.106+10979_106+1099 others(18): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | TTGTGTGT others(11): Show |
T | 4 | a0001c0001t0001g0092 a0001c0001t0046g0117 a0001c0001t0047g0122 others(1): Show |
4 | HG00438.hp2 HG02886.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+10975_106+1099 others(22): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450824 | TTGTGTGT others(13): Show |
T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.106+10973_106+1099 others(24): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78450824 | ||||||
| chr15:78450870 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.106+10989G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450870 | |||||||
| chr15:78450874 | A | G | 4 | a0003c0005t0009g0126 a0003c0005t0009g0127 a0003c0005t0009g0128 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+10993A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450874 | |||||||
| chr15:78450918 | A | G | 131 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(128): Show |
143 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.106+11037A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450918 | |||||||
| chr15:78450958 | A | C | 159 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(156): Show |
172 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.106+11077A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450958 | |||||||
| chr15:78450959 | A | T | 3 | a0001c0002t0003g0172 a0001c0002t0003g0173 a0001c0002t0003g0340 |
3 | HG00673.hp1 HG02056.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.106+11078A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78450959 | |||||||
| chr15:78451110 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.106+11229G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451110 | |||||||
| chr15:78451215 | C | G | 1 | a0001c0002t0003g0198 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.106+11334C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451215 | |||||||
| chr15:78451494 | C | T | 16 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(13): Show |
20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.107-11428C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451494 | |||||||
| chr15:78451588 | G | A | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-11334G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451588 | |||||||
| chr15:78451909 | C | T | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-11013C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451909 | |||||||
| chr15:78451928 | G | A | 28 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(25): Show |
29 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.107-10994G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451928 | |||||||
| chr15:78451950 | A | G | 275 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(272): Show |
299 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.107-10972A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78451950 | |||||||
| chr15:78452097 | G | A | 1 | a0001c0001t0011g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.107-10825G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452097 | |||||||
| chr15:78452151 | T | C | 2 | a0001c0001t0011g0144 a0001c0001t0011g0146 |
2 | NA18975.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.107-10771T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452151 | |||||||
| chr15:78452182 | G | A | 62 | a0001c0001t0041g0185 a0001c0002t0003g0003 a0001c0002t0003g0006 others(59): Show |
70 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.107-10740G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452182 | |||||||
| chr15:78452200 | C | T | 11 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(8): Show |
13 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(10): Show |
intron_variant | MODIFIER | c.107-10722C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452200 | |||||||
| chr15:78452258 | G | A | 62 | a0001c0001t0041g0185 a0001c0002t0003g0003 a0001c0002t0003g0006 others(59): Show |
70 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.107-10664G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452258 | |||||||
| chr15:78452515 | G | A | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-10407G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452515 | |||||||
| chr15:78452623 | G | A | 22 | a0001c0002t0003g0006 a0001c0002t0003g0014 a0001c0002t0003g0015 others(19): Show |
26 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.107-10299G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452623 | |||||||
| chr15:78452729 | A | G | 1 | a0001c0002t0003g0157 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.107-10193A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452729 | |||||||
| chr15:78452947 | A | G | 1 | a0001c0002t0005g0347 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.107-9975A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452947 | |||||||
| chr15:78452992 | T | C | 2 | a0001c0002t0003g0238 a0001c0002t0003g0239 |
2 | NA18962.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.107-9930T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78452992 | |||||||
| chr15:78453001 | T | A | 280 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(277): Show |
304 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.107-9921T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453001 | |||||||
| chr15:78453074 | C | T | 34 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0030 others(31): Show |
36 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.107-9848C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453074 | |||||||
| chr15:78453365 | C | T | 275 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(272): Show |
299 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.107-9557C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453365 | |||||||
| chr15:78453437 | A | G | 1 | a0001c0001t0002g0025 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.107-9485A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453437 | |||||||
| chr15:78453574 | G | A | 1 | a0001c0002t0005g0357 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.107-9348G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453574 | |||||||
| chr15:78453627 | C | T | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-9295C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453627 | |||||||
| chr15:78453710 | C | T | 5 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(2): Show |
5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-9212C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453710 | |||||||
| chr15:78453722 | A | G | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.107-9200A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453722 | |||||||
| chr15:78453776 | T | G | 25 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(22): Show |
25 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.107-9146T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453776 | |||||||
| chr15:78453952 | C | G | 9 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(6): Show |
11 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.107-8970C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78453952 | |||||||
| chr15:78454092 | A | G | 16 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(13): Show |
20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.107-8830A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454092 | |||||||
| chr15:78454317 | T | C | 6 | a0002c0003t0010g0013 a0002c0003t0010g0137 a0002c0003t0010g0138 others(3): Show |
7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-8605T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454317 | |||||||
| chr15:78454340 | G | A | 15 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(12): Show |
17 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.107-8582G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454340 | |||||||
| chr15:78454356 | T | G | 1 | a0002c0003t0010g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.107-8566T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454356 | |||||||
| chr15:78454497 | G | C | 2 | a0001c0002t0004g0248 a0001c0002t0004g0249 |
2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.107-8425G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454497 | |||||||
| chr15:78454613 | C | T | 21 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(18): Show |
25 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.107-8309C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454613 | |||||||
| chr15:78454713 | A | G | 28 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(25): Show |
29 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.107-8209A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454713 | |||||||
| chr15:78454841 | A | C | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-8081A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78454841 | |||||||
| chr15:78455012 | A | AGAGAATA others(313): Show |
1 | a0001c0001t0033g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.107-7897_107-7896i others(322): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78455012 | ||||||
| chr15:78455057 | G | T | 1 | a0001c0001t0002g0290 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.107-7865G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455057 | |||||||
| chr15:78455064 | C | T | 1 | a0001c0002t0004g0269 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.107-7858C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455064 | |||||||
| chr15:78455097 | T | C | 1 | a0001c0001t0009g0124 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.107-7825T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455097 | |||||||
| chr15:78455226 | A | G | 69 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(66): Show |
73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.107-7696A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455226 | |||||||
| chr15:78455539 | T | A | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.107-7383T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455539 | |||||||
| chr15:78455569 | G | GA | 29 | a0001c0001t0001g0093 a0001c0001t0007g0027 a0001c0001t0007g0321 others(26): Show |
30 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.107-7343dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78455569 | ||||||
| chr15:78455574 | AAAAAAG | A | 138 | a0001c0001t0041g0185 a0001c0002t0003g0003 a0001c0002t0003g0006 others(135): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.107-7342_107-7337d others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78455574 | ||||||
| chr15:78455695 | T | G | 1 | a0001c0001t0002g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.107-7227T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455695 | |||||||
| chr15:78455704 | T | G | 4 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0001t0011g0145 others(1): Show |
4 | HG01496.hp1 HG03486.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-7218T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455704 | |||||||
| chr15:78455769 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.107-7153A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455769 | |||||||
| chr15:78455778 | G | A | 2 | a0001c0002t0004g0019 a0001c0002t0004g0241 |
3 | NA18944.hp1 NA18968.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.107-7144G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455778 | |||||||
| chr15:78455897 | C | T | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-7025C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78455897 | |||||||
| chr15:78456060 | CTT | C | 15 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(12): Show |
17 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.107-6859_107-6858d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78456060 | ||||||
| chr15:78456104 | A | G | 1 | a0001c0002t0004g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.107-6818A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456104 | |||||||
| chr15:78456161 | A | C | 1 | a0001c0001t0002g0210 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.107-6761A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456161 | |||||||
| chr15:78456204 | T | A | 3 | a0001c0001t0046g0117 a0001c0001t0047g0122 a0001c0001t0048g0123 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.107-6718T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456204 | |||||||
| chr15:78456253 | G | A | 6 | a0001c0001t0002g0017 a0001c0001t0002g0207 a0001c0001t0002g0221 others(3): Show |
7 | NA18952.hp2 NA18959.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.107-6669G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456253 | |||||||
| chr15:78456271 | T | G | 2 | a0001c0001t0002g0149 a0001c0001t0002g0154 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.107-6651T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456271 | |||||||
| chr15:78456287 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0002g0225 |
2 | HG02074.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.107-6635G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456287 | |||||||
| chr15:78456302 | T | C | 1 | a0001c0002t0005g0367 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.107-6620T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456302 | |||||||
| chr15:78456432 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0060 |
5 | NA18961.hp2 NA18963.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-6490G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456432 | |||||||
| chr15:78456479 | A | G | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-6443A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456479 | |||||||
| chr15:78456513 | G | A | 21 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(18): Show |
25 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.107-6409G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456513 | |||||||
| chr15:78456665 | C | CA | 30 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0006g0002 others(27): Show |
33 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.107-6242dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78456665 | ||||||
| chr15:78456665 | CA | C | 27 | a0001c0001t0001g0038 a0001c0001t0001g0079 a0001c0001t0002g0207 others(24): Show |
27 | HG00408.hp2 HG01243.hp2 HG02074.hp1 others(24): Show |
intron_variant | MODIFIER | c.107-6242delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78456665 | ||||||
| chr15:78456764 | A | G | 4 | a0001c0004t0015g0040 a0001c0004t0015g0099 a0001c0004t0015g0100 others(1): Show |
4 | NA18978.hp2 NA18982.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-6158A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456764 | |||||||
| chr15:78456893 | C | T | 2 | a0001c0001t0001g0078 a0001c0012t0001g0105 |
2 | HG01069.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.107-6029C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456893 | |||||||
| chr15:78456968 | T | A | 2 | a0001c0004t0001g0094 a0001c0004t0016g0095 |
2 | NA18997.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.107-5954T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78456968 | |||||||
| chr15:78457156 | T | G | 1 | a0001c0002t0003g0203 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.107-5766T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457156 | |||||||
| chr15:78457266 | T | C | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.107-5656T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457266 | |||||||
| chr15:78457437 | A | T | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-5485A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457437 | |||||||
| chr15:78457476 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.107-5446T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457476 | |||||||
| chr15:78457710 | T | C | 69 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(66): Show |
73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.107-5212T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457710 | |||||||
| chr15:78457993 | T | C | 3 | a0001c0002t0005g0343 a0001c0002t0005g0344 a0001c0002t0005g0368 |
3 | HG00408.hp1 HG00609.hp2 HG02027.hp1 |
intron_variant | MODIFIER | c.107-4929T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78457993 | |||||||
| chr15:78458046 | A | T | 1 | a0001c0001t0001g0311 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.107-4876A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458046 | |||||||
| chr15:78458187 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0084 |
2 | NA18946.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.107-4735A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458187 | |||||||
| chr15:78458206 | G | C | 1 | a0001c0001t0033g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.107-4716G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458206 | |||||||
| chr15:78458207 | G | A | 140 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(137): Show |
152 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.107-4715G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458207 | |||||||
| chr15:78458564 | C | T | 15 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(12): Show |
17 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.107-4358C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458564 | |||||||
| chr15:78458761 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.107-4161T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458761 | |||||||
| chr15:78458778 | G | T | 2 | a0001c0002t0004g0254 a0001c0002t0004g0268 |
2 | NA18983.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.107-4144G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458778 | |||||||
| chr15:78458779 | G | T | 2 | a0001c0002t0004g0254 a0001c0002t0004g0268 |
2 | NA18983.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.107-4143G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458779 | |||||||
| chr15:78458810 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.107-4112G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458810 | |||||||
| chr15:78458957 | C | T | 1 | a0001c0002t0003g0175 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.107-3965C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78458957 | |||||||
| chr15:78459196 | A | T | 7 | a0001c0001t0033g0130 a0002c0003t0010g0013 a0002c0003t0010g0137 others(4): Show |
8 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-3726A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459196 | |||||||
| chr15:78459198 | A | T | 7 | a0001c0001t0033g0130 a0002c0003t0010g0013 a0002c0003t0010g0137 others(4): Show |
8 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.107-3724A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459198 | |||||||
| chr15:78459308 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.107-3614T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459308 | |||||||
| chr15:78459340 | G | GT | 33 | a0001c0002t0004g0004 a0001c0002t0005g0004 a0001c0002t0005g0028 others(30): Show |
35 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-3578dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78459340 | ||||||
| chr15:78459380 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.107-3542C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459380 | |||||||
| chr15:78459416 | C | G | 2 | a0001c0002t0004g0245 a0001c0002t0004g0246 |
2 | NA18980.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.107-3506C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459416 | |||||||
| chr15:78459419 | C | T | 1 | a0001c0002t0004g0249 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.107-3503C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459419 | |||||||
| chr15:78459420 | G | A | 2 | a0001c0002t0005g0369 a0001c0002t0005g0370 |
2 | HG00323.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.107-3502G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459420 | |||||||
| chr15:78459549 | C | T | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.107-3373C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459549 | |||||||
| chr15:78459619 | C | T | 140 | a0001c0001t0041g0185 a0001c0002t0003g0003 a0001c0002t0003g0006 others(137): Show |
153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.107-3303C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459619 | |||||||
| chr15:78459620 | G | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(83): Show |
98 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.107-3302G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459620 | |||||||
| chr15:78459630 | G | A | 1 | a0001c0002t0003g0238 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.107-3292G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459630 | |||||||
| chr15:78459650 | C | T | 1 | a0001c0002t0005g0346 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.107-3272C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459650 | |||||||
| chr15:78459772 | C | T | 280 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(277): Show |
304 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.107-3150C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459772 | |||||||
| chr15:78459812 | CCT | C | 67 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(64): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.107-3107_107-3106d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78459812 | ||||||
| chr15:78459846 | C | G | 33 | a0001c0002t0004g0004 a0001c0002t0005g0004 a0001c0002t0005g0028 others(30): Show |
35 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.107-3076C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78459846 | |||||||
| chr15:78460001 | G | A | 275 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(272): Show |
299 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.107-2921G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460001 | |||||||
| chr15:78460021 | G | A | 378 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(375): Show |
414 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(411): Show |
intron_variant | MODIFIER | c.107-2901G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460021 | |||||||
| chr15:78460050 | T | A | 2 | a0001c0001t0002g0208 a0001c0001t0002g0225 |
2 | HG02074.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.107-2872T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460050 | |||||||
| chr15:78460124 | C | G | 1 | a0001c0001t0002g0288 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.107-2798C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460124 | |||||||
| chr15:78460265 | T | G | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.107-2657T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460265 | |||||||
| chr15:78460405 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.107-2517A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460405 | |||||||
| chr15:78460551 | C | G | 1 | a0001c0002t0005g0356 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.107-2371C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460551 | |||||||
| chr15:78460800 | C | G | 1 | a0001c0002t0003g0198 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.107-2122C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78460800 | |||||||
| chr15:78461029 | A | G | 131 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(128): Show |
143 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.107-1893A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461029 | |||||||
| chr15:78461101 | GAT | G | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1819_107-1818d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78461101 | ||||||
| chr15:78461103 | T | G | 1 | a0001c0001t0041g0185 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.107-1819T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461103 | |||||||
| chr15:78461133 | A | G | 6 | a0002c0003t0010g0013 a0002c0003t0010g0137 a0002c0003t0010g0138 others(3): Show |
7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-1789A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461133 | |||||||
| chr15:78461199 | C | G | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1723C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461199 | |||||||
| chr15:78461225 | CAGGACAT others(14): Show |
C | 1 | a0004c0007t0019g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.107-1696_107-1676d others(23): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461225 | |||||||
| chr15:78461330 | A | G | 2 | a0001c0001t0011g0144 a0001c0001t0011g0146 |
2 | NA18975.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.107-1592A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461330 | |||||||
| chr15:78461361 | T | TAAAG | 4 | a0003c0005t0009g0126 a0003c0005t0009g0127 a0003c0005t0009g0128 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-1559_107-1556d others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr15 | 78461361 | ||||||
| chr15:78461604 | G | A | 6 | a0002c0003t0010g0013 a0002c0003t0010g0137 a0002c0003t0010g0138 others(3): Show |
7 | HG01109.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.107-1318G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461604 | |||||||
| chr15:78461658 | A | G | 141 | a0001c0001t0004g0104 a0001c0001t0016g0059 a0001c0001t0041g0185 others(138): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.107-1264A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461658 | |||||||
| chr15:78461672 | G | T | 1 | a0001c0001t0016g0045 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.107-1250G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461672 | |||||||
| chr15:78461760 | A | G | 74 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(71): Show |
79 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.107-1162A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78461760 | |||||||
| chr15:78462027 | T | A | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.107-895T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462027 | |||||||
| chr15:78462052 | A | G | 4 | a0001c0002t0004g0022 a0001c0002t0004g0251 a0001c0002t0004g0267 others(1): Show |
4 | HG01891.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-870A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462052 | |||||||
| chr15:78462095 | A | G | 1 | a0001c0002t0003g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.107-827A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462095 | |||||||
| chr15:78462233 | T | C | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.107-689T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462233 | |||||||
| chr15:78462239 | T | C | 1 | a0001c0006t0025g0131 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.107-683T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462239 | |||||||
| chr15:78462366 | A | T | 1 | a0001c0002t0003g0184 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.107-556A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462366 | |||||||
| chr15:78462388 | A | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG02165.hp1 NA18946.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-534A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462388 | |||||||
| chr15:78462521 | T | C | 69 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(66): Show |
73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.107-401T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462521 | |||||||
| chr15:78462660 | C | A | 5 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(2): Show |
5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-262C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462660 | |||||||
| chr15:78462779 | C | T | 1 | a0001c0002t0003g0188 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.107-143C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462779 | |||||||
| chr15:78462820 | A | G | 2 | a0001c0001t0002g0147 a0001c0001t0002g0152 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.107-102A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462820 | |||||||
| chr15:78462827 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.107-95A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462827 | |||||||
| chr15:78462853 | T | G | 1 | a0001c0001t0001g0304 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.107-69T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462853 | |||||||
| chr15:78462900 | T | G | 3 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0022g0247 |
3 | HG01243.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.107-22T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 2/21 | chr15 | 78462900 | |||||||
| chr15:78463341 | T | C | 2 | a0001c0002t0003g0179 a0001c0002t0017g0180 |
2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.272+254T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78463341 | |||||||
| chr15:78463376 | G | A | 1 | a0001c0002t0003g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.272+289G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78463376 | |||||||
| chr15:78463406 | A | C | 1 | a0001c0001t0001g0303 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.272+319A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78463406 | |||||||
| chr15:78463490 | G | GT | 9 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(6): Show |
10 | HG00673.hp1 HG02451.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.272+404dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr15 | 78463490 | ||||||
| chr15:78463492 | G | T | 346 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(343): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.272+405G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78463492 | |||||||
| chr15:78463895 | A | T | 16 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(13): Show |
20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.272+808A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78463895 | |||||||
| chr15:78464167 | A | G | 16 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(13): Show |
20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.272+1080A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78464167 | |||||||
| chr15:78464220 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.273-1031G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78464220 | |||||||
| chr15:78464829 | C | T | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.273-422C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78464829 | |||||||
| chr15:78464890 | G | A | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.273-361G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78464890 | |||||||
| chr15:78465028 | T | C | 1 | a0001c0001t0033g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.273-223T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78465028 | |||||||
| chr15:78465033 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.273-218A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78465033 | |||||||
| chr15:78465088 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.273-163T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 3/21 | chr15 | 78465088 | |||||||
| chr15:78465530 | C | G | 3 | a0001c0001t0002g0218 a0001c0001t0002g0219 a0001c0001t0002g0220 |
3 | HG00738.hp2 HG00741.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.410+142C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465530 | |||||||
| chr15:78465550 | T | C | 69 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(66): Show |
73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.410+162T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465550 | |||||||
| chr15:78465571 | C | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(103): Show |
118 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.410+183C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465571 | |||||||
| chr15:78465617 | C | T | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+229C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465617 | |||||||
| chr15:78465635 | C | A | 1 | a0001c0001t0008g0316 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.410+247C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465635 | |||||||
| chr15:78465871 | G | A | 345 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(342): Show |
375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.411-400G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465871 | |||||||
| chr15:78465915 | T | A | 1 | a0001c0001t0033g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.411-356T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465915 | |||||||
| chr15:78465956 | T | A | 2 | a0001c0002t0005g0358 a0001c0002t0005g0359 |
2 | HG01516.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.411-315T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465956 | |||||||
| chr15:78465970 | TA | T | 6 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0241 others(3): Show |
8 | NA18944.hp1 NA18949.hp1 NA18968.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-300delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465970 | |||||||
| chr15:78465982 | A | G | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-289A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78465982 | |||||||
| chr15:78466099 | T | A | 5 | a0001c0001t0006g0011 a0001c0006t0024g0133 a0001c0006t0024g0134 others(2): Show |
6 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.411-172T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78466099 | |||||||
| chr15:78466105 | A | G | 1 | a0001c0002t0003g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.411-166A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78466105 | |||||||
| chr15:78466136 | G | C | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-135G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78466136 | |||||||
| chr15:78466239 | G | A | 2 | a0001c0001t0046g0117 a0001c0001t0048g0123 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.411-32G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 4/21 | chr15 | 78466239 | |||||||
| chr15:78466496 | G | T | 3 | a0001c0001t0046g0117 a0001c0001t0047g0122 a0001c0001t0048g0123 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.629+7G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466496 | |||||||
| chr15:78466511 | A | C | 375 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(372): Show |
410 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.629+22A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466511 | |||||||
| chr15:78466560 | T | TC | 376 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(373): Show |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.629+72dupC | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr15 | 78466560 | ||||||
| chr15:78466578 | A | T | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.629+89A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466578 | |||||||
| chr15:78466913 | A | G | 2 | a0001c0001t0002g0149 a0001c0001t0002g0154 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.629+424A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466913 | |||||||
| chr15:78466922 | A | T | 1 | a0001c0001t0001g0082 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.629+433A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466922 | |||||||
| chr15:78466986 | GCAGGTGG others(12): Show |
G | 69 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(66): Show |
73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.629+502_629+520del others(19): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr15 | 78466986 | ||||||
| chr15:78466989 | G | A | 1 | a0001c0002t0004g0004 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.629+500G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78466989 | |||||||
| chr15:78467006 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(97): Show |
112 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.629+517C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467006 | |||||||
| chr15:78467012 | T | G | 1 | a0004c0007t0019g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.629+523T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467012 | |||||||
| chr15:78467034 | C | T | 346 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(343): Show |
376 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(373): Show |
intron_variant | MODIFIER | c.629+545C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467034 | |||||||
| chr15:78467085 | C | G | 2 | a0001c0001t0002g0211 a0001c0001t0002g0235 |
2 | NA18961.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.629+596C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467085 | |||||||
| chr15:78467208 | C | CA | 147 | a0001c0001t0001g0052 a0001c0001t0001g0065 a0001c0001t0001g0066 others(144): Show |
160 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.629+736dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr15 | 78467208 | ||||||
| chr15:78467538 | A | T | 1 | a0004c0007t0019g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.629+1049A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467538 | |||||||
| chr15:78467662 | C | A | 1 | a0001c0001t0002g0152 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.629+1173C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467662 | |||||||
| chr15:78467945 | G | A | 69 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(66): Show |
73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.629+1456G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78467945 | |||||||
| chr15:78468002 | G | A | 69 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(66): Show |
73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.629+1513G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468002 | |||||||
| chr15:78468232 | C | T | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.629+1743C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468232 | |||||||
| chr15:78468271 | G | T | 1 | a0001c0001t0033g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.629+1782G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468271 | |||||||
| chr15:78468493 | CT | C | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.629+2006delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr15 | 78468493 | ||||||
| chr15:78468509 | G | A | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.629+2020G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468509 | |||||||
| chr15:78468542 | C | CT | 84 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(81): Show |
92 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(89): Show |
intron_variant | MODIFIER | c.630-1977dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr15 | 78468542 | ||||||
| chr15:78468568 | A | G | 2 | a0001c0002t0003g0188 a0001c0002t0003g0205 |
2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.630-1964A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468568 | |||||||
| chr15:78468568 | A | T | 1 | a0001c0002t0012g0274 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.630-1964A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468568 | |||||||
| chr15:78468576 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(222): Show |
246 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(243): Show |
intron_variant | MODIFIER | c.630-1956G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468576 | |||||||
| chr15:78468942 | T | A | 1 | a0004c0007t0019g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.630-1590T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468942 | |||||||
| chr15:78468969 | A | T | 1 | a0001c0001t0002g0215 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.630-1563A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78468969 | |||||||
| chr15:78469072 | C | G | 34 | a0001c0002t0004g0004 a0001c0002t0005g0004 a0001c0002t0005g0028 others(31): Show |
36 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.630-1460C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469072 | |||||||
| chr15:78469124 | A | C | 1 | a0001c0001t0002g0215 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.630-1408A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469124 | |||||||
| chr15:78469137 | T | G | 1 | a0001c0001t0014g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.630-1395T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469137 | |||||||
| chr15:78469164 | T | A | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.630-1368T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469164 | |||||||
| chr15:78469282 | G | C | 1 | a0001c0002t0005g0346 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.630-1250G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469282 | |||||||
| chr15:78469318 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.630-1214G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469318 | |||||||
| chr15:78469338 | C | G | 1 | a0001c0001t0002g0214 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.630-1194C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469338 | |||||||
| chr15:78469355 | A | G | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.630-1177A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469355 | |||||||
| chr15:78469442 | G | A | 6 | a0001c0002t0003g0184 a0001c0002t0003g0189 a0001c0002t0003g0190 others(3): Show |
6 | HG01069.hp2 HG01106.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.630-1090G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469442 | |||||||
| chr15:78469491 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.630-1041G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469491 | |||||||
| chr15:78469501 | G | A | 377 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(374): Show |
413 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(410): Show |
intron_variant | MODIFIER | c.630-1031G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469501 | |||||||
| chr15:78469533 | G | C | 3 | a0001c0001t0041g0185 a0001c0002t0003g0195 a0001c0002t0003g0198 |
3 | HG00544.hp1 NA19005.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.630-999G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469533 | |||||||
| chr15:78469550 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.630-982C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469550 | |||||||
| chr15:78469611 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.630-921T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469611 | |||||||
| chr15:78469859 | G | A | 1 | a0001c0002t0038g0165 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.630-673G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469859 | |||||||
| chr15:78469971 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(102): Show |
117 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.630-561A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469971 | |||||||
| chr15:78469973 | A | G | 4 | a0003c0005t0009g0126 a0003c0005t0009g0127 a0003c0005t0009g0128 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.630-559A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78469973 | |||||||
| chr15:78470006 | A | C | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.630-526A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78470006 | |||||||
| chr15:78470049 | T | C | 2 | a0001c0002t0039g0202 a0001c0002t0040g0201 |
2 | HG03491.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.630-483T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78470049 | |||||||
| chr15:78470142 | A | G | 375 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(372): Show |
410 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.630-390A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78470142 | |||||||
| chr15:78470174 | A | G | 5 | a0001c0001t0020g0135 a0001c0001t0020g0136 a0001c0001t0046g0117 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.630-358A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78470174 | |||||||
| chr15:78470286 | T | C | 2 | a0001c0002t0003g0238 a0001c0002t0003g0239 |
2 | NA18962.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.630-246T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 5/21 | chr15 | 78470286 | |||||||
| chr15:78470689 | C | CT | 147 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0074 others(144): Show |
160 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(157): Show |
intron_variant | MODIFIER | c.699+111dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr15 | 78470689 | ||||||
| chr15:78470689 | C | CTT | 12 | a0001c0001t0001g0042 a0001c0001t0002g0209 a0001c0002t0003g0157 others(9): Show |
12 | HG01081.hp2 HG01123.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.699+110_699+111dup others(2): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr15 | 78470689 | ||||||
| chr15:78470689 | C | T | 1 | a0004c0007t0019g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.699+88C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470689 | |||||||
| chr15:78470689 | CT | C | 21 | a0001c0001t0001g0046 a0001c0001t0001g0078 a0001c0001t0001g0311 others(18): Show |
25 | HG01069.hp1 HG01243.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.699+111delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr15 | 78470689 | ||||||
| chr15:78470726 | G | A | 1 | a0001c0002t0017g0176 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.699+125G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470726 | |||||||
| chr15:78470758 | G | C | 1 | a0001c0001t0008g0314 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.699+157G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470758 | |||||||
| chr15:78470840 | G | A | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.699+239G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470840 | |||||||
| chr15:78470848 | G | C | 376 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(373): Show |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.699+247G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470848 | |||||||
| chr15:78470901 | G | A | 3 | a0001c0002t0003g0192 a0001c0002t0003g0193 a0001c0002t0003g0197 |
3 | HG00597.hp2 HG02129.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.699+300G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470901 | |||||||
| chr15:78470931 | G | A | 5 | a0001c0001t0007g0332 a0001c0001t0013g0328 a0001c0001t0013g0329 others(2): Show |
5 | HG03834.hp1 NA18947.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.699+330G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470931 | |||||||
| chr15:78470933 | A | G | 1 | a0001c0002t0004g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.699+332A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470933 | |||||||
| chr15:78470946 | C | T | 1 | a0001c0002t0003g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.699+345C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470946 | |||||||
| chr15:78470947 | G | A | 3 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0043g0294 |
3 | HG01978.hp2 HG02004.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.699+346G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470947 | |||||||
| chr15:78470951 | C | T | 2 | a0001c0002t0017g0176 a0001c0002t0017g0186 |
2 | HG00323.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.699+350C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470951 | |||||||
| chr15:78470955 | C | G | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.699+354C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470955 | |||||||
| chr15:78470999 | T | G | 1 | a0004c0007t0019g0293 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.699+398T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78470999 | |||||||
| chr15:78471275 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(102): Show |
117 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.700-466C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471275 | |||||||
| chr15:78471302 | C | T | 1 | a0001c0001t0011g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.700-439C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471302 | |||||||
| chr15:78471387 | G | A | 1 | a0001c0001t0008g0319 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.700-354G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471387 | |||||||
| chr15:78471467 | C | T | 376 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(373): Show |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.700-274C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471467 | |||||||
| chr15:78471554 | T | G | 1 | a0001c0002t0012g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.700-187T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471554 | |||||||
| chr15:78471597 | T | C | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.700-144T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471597 | |||||||
| chr15:78471673 | T | C | 16 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(13): Show |
20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.700-68T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 6/21 | chr15 | 78471673 | |||||||
| chr15:78471943 | A | G | 67 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(64): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.883+19A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78471943 | |||||||
| chr15:78471982 | G | A | 67 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(64): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.883+58G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78471982 | |||||||
| chr15:78472179 | T | C | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.883+255T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472179 | |||||||
| chr15:78472237 | G | C | 1 | a0001c0002t0003g0172 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.883+313G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472237 | |||||||
| chr15:78472407 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.883+483C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472407 | |||||||
| chr15:78472524 | G | A | 5 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(2): Show |
5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.883+600G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472524 | |||||||
| chr15:78472557 | C | T | 2 | a0001c0001t0020g0135 a0001c0001t0020g0136 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.883+633C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472557 | |||||||
| chr15:78472567 | A | G | 5 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(2): Show |
5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.883+643A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472567 | |||||||
| chr15:78472780 | G | T | 77 | a0001c0002t0004g0004 a0001c0002t0004g0019 a0001c0002t0004g0020 others(74): Show |
82 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.884-462G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472780 | |||||||
| chr15:78472847 | C | T | 67 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(64): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.884-395C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472847 | |||||||
| chr15:78472927 | A | C | 1 | a0001c0002t0005g0354 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.884-315A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472927 | |||||||
| chr15:78472944 | A | G | 5 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(2): Show |
5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-298A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472944 | |||||||
| chr15:78472948 | T | G | 141 | a0001c0001t0004g0104 a0001c0002t0003g0003 a0001c0002t0003g0006 others(138): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.884-294T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78472948 | |||||||
| chr15:78473051 | G | GT | 3 | a0001c0001t0001g0068 a0001c0001t0001g0306 a0001c0002t0003g0197 |
3 | HG01175.hp1 NA18967.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.884-186dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr15 | 78473051 | ||||||
| chr15:78473120 | A | G | 1 | a0001c0002t0004g0269 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.884-122A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 7/21 | chr15 | 78473120 | |||||||
| chr15:78473404 | C | T | 2 | a0001c0002t0004g0253 a0001c0002t0004g0262 |
2 | NA18951.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1023+23C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473404 | |||||||
| chr15:78473611 | T | C | 1 | a0001c0002t0003g0198 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1023+230T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473611 | |||||||
| chr15:78473852 | T | A | 139 | a0001c0001t0004g0104 a0001c0002t0003g0003 a0001c0002t0003g0006 others(136): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1023+471T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473852 | |||||||
| chr15:78473853 | A | T | 1 | a0001c0001t0001g0301 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1023+472A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473853 | |||||||
| chr15:78473866 | A | T | 39 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(36): Show |
42 | HG00280.hp1 HG00423.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.1023+485A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473866 | |||||||
| chr15:78473908 | A | G | 34 | a0001c0002t0004g0004 a0001c0002t0005g0004 a0001c0002t0005g0028 others(31): Show |
36 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.1023+527A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473908 | |||||||
| chr15:78473969 | T | C | 1 | a0001c0002t0017g0186 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1023+588T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78473969 | |||||||
| chr15:78474084 | C | T | 1 | a0001c0001t0030g0073 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1023+703C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474084 | |||||||
| chr15:78474287 | C | T | 138 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(135): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1023+906C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474287 | |||||||
| chr15:78474345 | T | C | 4 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0001t0011g0145 others(1): Show |
4 | HG01496.hp1 HG03486.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+964T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474345 | |||||||
| chr15:78474396 | A | G | 21 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(18): Show |
25 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1023+1015A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474396 | |||||||
| chr15:78474400 | A | G | 4 | a0003c0005t0009g0126 a0003c0005t0009g0127 a0003c0005t0009g0128 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1023+1019A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474400 | |||||||
| chr15:78474558 | A | G | 1 | a0001c0002t0004g0248 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1023+1177A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474558 | |||||||
| chr15:78474918 | G | A | 1 | a0001c0002t0004g0023 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1024-1270G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474918 | |||||||
| chr15:78474980 | G | A | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1024-1208G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78474980 | |||||||
| chr15:78475004 | G | A | 128 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(125): Show |
140 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1024-1184G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475004 | |||||||
| chr15:78475049 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1024-1139G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475049 | |||||||
| chr15:78475061 | C | CA | 28 | a0001c0001t0002g0018 a0001c0001t0002g0121 a0001c0001t0002g0209 others(25): Show |
29 | HG00741.hp2 HG01123.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.1024-1102dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | ||||||
| chr15:78475061 | C | CAAA | 10 | a0001c0001t0006g0002 a0001c0001t0006g0010 a0001c0001t0006g0108 others(7): Show |
13 | HG01346.hp2 HG02451.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1024-1104_1024-110 others(7): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | ||||||
| chr15:78475061 | C | CAAAA | 5 | a0001c0001t0006g0009 a0001c0001t0006g0011 a0001c0001t0006g0109 others(2): Show |
6 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024-1105_1024-110 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | ||||||
| chr15:78475061 | C | CAAAAA | 5 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(2): Show |
6 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024-1106_1024-110 others(9): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | ||||||
| chr15:78475061 | CA | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(198): Show |
225 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1024-1102delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | ||||||
| chr15:78475061 | CAA | C | 6 | a0001c0001t0001g0098 a0001c0001t0001g0313 a0001c0002t0004g0267 others(3): Show |
6 | HG00280.hp1 HG01099.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024-1103_1024-110 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475061 | ||||||
| chr15:78475164 | C | T | 1 | a0001c0002t0004g0264 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1024-1024C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475164 | |||||||
| chr15:78475206 | C | G | 1 | a0001c0002t0012g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1024-982C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475206 | |||||||
| chr15:78475285 | A | G | 4 | a0003c0005t0009g0126 a0003c0005t0009g0127 a0003c0005t0009g0128 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024-903A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475285 | |||||||
| chr15:78475345 | A | G | 16 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(13): Show |
20 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1024-843A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475345 | |||||||
| chr15:78475508 | C | T | 138 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(135): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1024-680C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475508 | |||||||
| chr15:78475682 | C | CA | 69 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(66): Show |
73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.1024-494dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | 78475682 | ||||||
| chr15:78475765 | T | G | 3 | a0001c0002t0005g0369 a0001c0002t0005g0370 a0001c0002t0005g0371 |
3 | HG00323.hp2 HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1024-423T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475765 | |||||||
| chr15:78475801 | G | A | 1 | a0002c0003t0010g0137 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1024-387G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475801 | |||||||
| chr15:78475817 | G | A | 2 | a0001c0002t0039g0202 a0001c0002t0040g0201 |
2 | HG03491.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1024-371G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475817 | |||||||
| chr15:78475825 | C | G | 104 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(101): Show |
116 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1024-363C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475825 | |||||||
| chr15:78475974 | C | A | 1 | a0001c0002t0005g0364 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1024-214C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78475974 | |||||||
| chr15:78476043 | T | C | 1 | a0001c0002t0003g0169 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1024-145T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 8/21 | chr15 | 78476043 | |||||||
| chr15:78476529 | C | G | 138 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(135): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1195+170C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476529 | |||||||
| chr15:78476536 | T | C | 3 | a0001c0001t0046g0117 a0001c0001t0047g0122 a0001c0001t0048g0123 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1195+177T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476536 | |||||||
| chr15:78476752 | C | T | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.1195+393C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476752 | |||||||
| chr15:78476771 | A | C | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1195+412A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476771 | |||||||
| chr15:78476788 | A | G | 140 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(137): Show |
153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1195+429A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476788 | |||||||
| chr15:78476957 | C | T | 2 | a0001c0002t0005g0358 a0001c0002t0005g0359 |
2 | HG01516.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1195+598C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476957 | |||||||
| chr15:78476964 | A | G | 1 | a0001c0001t0013g0331 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1195+605A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476964 | |||||||
| chr15:78476964 | A | T | 1 | a0001c0001t0001g0313 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1195+605A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78476964 | |||||||
| chr15:78477187 | C | T | 2 | a0001c0001t0020g0135 a0001c0001t0020g0136 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1195+828C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477187 | |||||||
| chr15:78477344 | T | G | 1 | a0001c0001t0002g0287 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1196-953T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477344 | |||||||
| chr15:78477401 | T | C | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1196-896T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477401 | |||||||
| chr15:78477460 | T | C | 1 | a0001c0002t0017g0186 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1196-837T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477460 | |||||||
| chr15:78477560 | A | G | 1 | a0001c0001t0007g0339 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1196-737A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477560 | |||||||
| chr15:78477628 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1196-669T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477628 | |||||||
| chr15:78477677 | C | T | 376 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(373): Show |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.1196-620C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477677 | |||||||
| chr15:78477690 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1196-607C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78477690 | |||||||
| chr15:78478020 | G | A | 2 | a0001c0001t0020g0135 a0001c0001t0020g0136 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1196-277G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78478020 | |||||||
| chr15:78478076 | A | G | 63 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(60): Show |
67 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.1196-221A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78478076 | |||||||
| chr15:78478081 | T | TA | 43 | a0001c0001t0001g0033 a0001c0001t0002g0017 a0001c0001t0002g0018 others(40): Show |
45 | HG00738.hp2 HG00741.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.1196-198dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr15 | 78478081 | ||||||
| chr15:78478081 | TA | T | 28 | a0001c0001t0001g0058 a0001c0001t0001g0078 a0001c0001t0001g0304 others(25): Show |
32 | HG00323.hp2 HG01069.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1196-198delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr15 | 78478081 | ||||||
| chr15:78478212 | C | T | 1 | a0001c0002t0005g0365 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1196-85C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 9/21 | chr15 | 78478212 | |||||||
| chr15:78478575 | G | A | 67 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(64): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1296+178G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78478575 | |||||||
| chr15:78478829 | C | T | 2 | a0001c0001t0006g0111 a0001c0001t0006g0113 |
2 | HG02717.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1296+432C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78478829 | |||||||
| chr15:78478831 | C | CA | 4 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+435dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78478831 | ||||||
| chr15:78478844 | T | C | 67 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(64): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1296+447T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78478844 | |||||||
| chr15:78479093 | T | G | 1 | a0001c0001t0008g0319 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1296+696T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479093 | |||||||
| chr15:78479204 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(104): Show |
119 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1296+807C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479204 | |||||||
| chr15:78479399 | A | AT | 14 | a0001c0001t0001g0033 a0001c0001t0002g0024 a0001c0001t0002g0025 others(11): Show |
16 | HG01074.hp2 HG01255.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1296+1018dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78479399 | ||||||
| chr15:78479399 | A | ATT | 15 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(12): Show |
19 | HG01243.hp1 HG01346.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1296+1017_1296+101 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78479399 | ||||||
| chr15:78479657 | T | C | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1296+1260T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479657 | |||||||
| chr15:78479728 | T | G | 375 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(372): Show |
410 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.1296+1331T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479728 | |||||||
| chr15:78479748 | T | G | 1 | a0001c0002t0004g0266 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1296+1351T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479748 | |||||||
| chr15:78479818 | G | A | 11 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0096 others(8): Show |
11 | HG00438.hp2 NA18956.hp2 NA18978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1296+1421G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479818 | |||||||
| chr15:78479832 | G | A | 1 | a0001c0002t0004g0272 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1296+1435G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78479832 | |||||||
| chr15:78479919 | T | TA | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(142): Show |
164 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1296+1539dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78479919 | ||||||
| chr15:78479919 | T | TAA | 62 | a0001c0001t0001g0060 a0001c0001t0001g0096 a0001c0001t0002g0017 others(59): Show |
66 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.1296+1538_1296+153 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78479919 | ||||||
| chr15:78479919 | T | TAAA | 6 | a0001c0001t0001g0072 a0001c0001t0002g0030 a0001c0001t0002g0234 others(3): Show |
6 | HG01261.hp1 NA18973.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1296+1537_1296+153 others(7): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78479919 | ||||||
| chr15:78480298 | T | C | 2 | a0001c0001t0001g0069 a0001c0001t0030g0073 |
2 | NA19003.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1296+1901T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480298 | |||||||
| chr15:78480334 | A | G | 34 | a0001c0002t0004g0004 a0001c0002t0005g0004 a0001c0002t0005g0028 others(31): Show |
36 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.1296+1937A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480334 | |||||||
| chr15:78480464 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(104): Show |
119 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1296+2067C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480464 | |||||||
| chr15:78480564 | C | A | 1 | a0001c0002t0003g0188 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1296+2167C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480564 | |||||||
| chr15:78480603 | C | T | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1296+2206C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480603 | |||||||
| chr15:78480604 | G | A | 67 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(64): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1296+2207G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480604 | |||||||
| chr15:78480618 | G | A | 5 | a0001c0001t0001g0302 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
5 | HG00558.hp2 HG02015.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.1296+2221G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480618 | |||||||
| chr15:78480663 | T | C | 7 | a0001c0002t0005g0343 a0001c0002t0005g0344 a0001c0002t0005g0345 others(4): Show |
7 | HG00408.hp1 HG00609.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1296+2266T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480663 | |||||||
| chr15:78480674 | A | G | 367 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(364): Show |
401 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(398): Show |
intron_variant | MODIFIER | c.1296+2277A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480674 | |||||||
| chr15:78480686 | T | TA | 19 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0055 others(16): Show |
23 | HG01243.hp1 HG01256.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.1296+2309dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78480686 | ||||||
| chr15:78480686 | T | TAA | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(91): Show |
107 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1296+2308_1296+230 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78480686 | ||||||
| chr15:78480686 | T | TAAA | 174 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0001t0001g0066 others(171): Show |
188 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.1296+2307_1296+230 others(7): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78480686 | ||||||
| chr15:78480686 | T | TAAAA | 52 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0118 others(49): Show |
54 | HG00673.hp1 HG01074.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.1296+2306_1296+230 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78480686 | ||||||
| chr15:78480686 | T | TAAAAA | 32 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0119 others(29): Show |
34 | HG00738.hp2 HG00741.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.1296+2305_1296+230 others(9): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78480686 | ||||||
| chr15:78480716 | G | A | 1 | a0001c0002t0004g0275 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1296+2319G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480716 | |||||||
| chr15:78480720 | G | T | 2 | a0001c0002t0005g0358 a0001c0002t0005g0359 |
2 | HG01516.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1296+2323G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480720 | |||||||
| chr15:78480731 | C | T | 8 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0002g0149 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1296+2334C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480731 | |||||||
| chr15:78480776 | G | A | 4 | a0001c0001t0001g0297 a0001c0001t0001g0298 a0001c0001t0001g0300 others(1): Show |
4 | HG02280.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296+2379G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480776 | |||||||
| chr15:78480801 | A | T | 1 | a0001c0001t0002g0284 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1296+2404A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78480801 | |||||||
| chr15:78481008 | C | CA | 10 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0002g0210 others(7): Show |
10 | HG01175.hp1 HG01952.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1297-2295dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481008 | ||||||
| chr15:78481078 | G | A | 2 | a0001c0002t0003g0188 a0001c0002t0003g0205 |
2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1297-2240G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481078 | |||||||
| chr15:78481093 | A | T | 21 | a0001c0001t0006g0002 a0001c0001t0006g0009 a0001c0001t0006g0010 others(18): Show |
25 | HG01243.hp1 HG01346.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1297-2225A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481093 | |||||||
| chr15:78481174 | C | A | 376 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(373): Show |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.1297-2144C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481174 | |||||||
| chr15:78481204 | G | A | 3 | a0001c0002t0004g0248 a0001c0002t0004g0249 a0001c0002t0022g0247 |
3 | HG01243.hp2 HG02280.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1297-2114G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481204 | |||||||
| chr15:78481210 | A | G | 1 | a0001c0002t0003g0374 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1297-2108A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481210 | |||||||
| chr15:78481246 | A | G | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1297-2072A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481246 | |||||||
| chr15:78481332 | A | C | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297-1986A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481332 | |||||||
| chr15:78481346 | A | G | 375 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(372): Show |
410 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.1297-1972A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481346 | |||||||
| chr15:78481347 | C | T | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297-1971C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481347 | |||||||
| chr15:78481351 | C | T | 63 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(60): Show |
67 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(64): Show |
intron_variant | MODIFIER | c.1297-1967C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481351 | |||||||
| chr15:78481363 | C | T | 2 | a0001c0002t0003g0179 a0001c0002t0017g0180 |
2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1297-1955C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481363 | |||||||
| chr15:78481366 | C | CT | 8 | a0001c0001t0002g0209 a0001c0001t0007g0324 a0001c0001t0046g0117 others(5): Show |
8 | HG02886.hp1 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1297-1942dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481366 | ||||||
| chr15:78481388 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1297-1930G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481388 | |||||||
| chr15:78481522 | A | AT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(82): Show |
97 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1297-1780dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481522 | ||||||
| chr15:78481522 | A | ATT | 188 | a0001c0001t0001g0055 a0001c0001t0001g0096 a0001c0001t0001g0295 others(185): Show |
205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.1297-1781_1297-178 others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481522 | ||||||
| chr15:78481522 | A | ATTT | 83 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(80): Show |
88 | HG00597.hp2 HG00738.hp2 HG01074.hp2 others(85): Show |
intron_variant | MODIFIER | c.1297-1782_1297-178 others(7): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481522 | ||||||
| chr15:78481522 | A | ATTTT | 11 | a0001c0001t0002g0121 a0001c0001t0002g0218 a0001c0001t0002g0226 others(8): Show |
11 | HG00741.hp1 HG02083.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.1297-1783_1297-178 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78481522 | ||||||
| chr15:78481566 | C | T | 62 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(59): Show |
70 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1297-1752C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481566 | |||||||
| chr15:78481591 | T | C | 2 | a0001c0001t0002g0149 a0001c0001t0002g0154 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1297-1727T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481591 | |||||||
| chr15:78481592 | C | T | 2 | a0001c0001t0002g0149 a0001c0001t0002g0154 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1297-1726C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481592 | |||||||
| chr15:78481781 | T | C | 1 | a0001c0002t0005g0342 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1297-1537T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481781 | |||||||
| chr15:78481929 | C | T | 140 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(137): Show |
153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1297-1389C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78481929 | |||||||
| chr15:78482032 | A | G | 140 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(137): Show |
153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1297-1286A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482032 | |||||||
| chr15:78482090 | C | T | 2 | a0001c0001t0002g0147 a0001c0001t0002g0152 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1297-1228C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482090 | |||||||
| chr15:78482334 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(99): Show |
114 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1297-984A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482334 | |||||||
| chr15:78482395 | A | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0046 others(9): Show |
12 | HG00099.hp1 HG01256.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1297-923A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482395 | |||||||
| chr15:78482640 | AT | A | 8 | a0001c0002t0004g0004 a0001c0002t0005g0004 a0001c0002t0005g0342 others(5): Show |
10 | HG00099.hp2 HG01081.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.1297-675delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78482640 | ||||||
| chr15:78482643 | T | C | 2 | a0001c0006t0025g0131 a0001c0006t0025g0132 |
2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1297-675T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482643 | |||||||
| chr15:78482722 | T | C | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0054 |
3 | HG03490.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1297-596T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482722 | |||||||
| chr15:78482751 | G | GT | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(105): Show |
120 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1297-553dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78482751 | ||||||
| chr15:78482751 | G | GTT | 6 | a0001c0001t0001g0033 a0001c0001t0001g0076 a0001c0001t0001g0077 others(3): Show |
6 | HG00438.hp2 HG01928.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297-554_1297-553d others(4): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr15 | 78482751 | ||||||
| chr15:78482826 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1297-492C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482826 | |||||||
| chr15:78482834 | G | A | 2 | a0001c0001t0002g0211 a0001c0001t0002g0235 |
2 | NA18961.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1297-484G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482834 | |||||||
| chr15:78482892 | C | T | 3 | a0001c0001t0046g0117 a0001c0001t0047g0122 a0001c0001t0048g0123 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1297-426C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482892 | |||||||
| chr15:78482929 | C | T | 2 | a0001c0001t0002g0149 a0001c0001t0002g0154 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1297-389C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482929 | |||||||
| chr15:78482987 | C | T | 1 | a0001c0002t0044g0174 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1297-331C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78482987 | |||||||
| chr15:78483039 | C | G | 67 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(64): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.1297-279C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78483039 | |||||||
| chr15:78483130 | G | T | 2 | a0001c0001t0001g0078 a0001c0012t0001g0105 |
2 | HG01069.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1297-188G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78483130 | |||||||
| chr15:78483178 | G | A | 2 | a0001c0001t0002g0147 a0001c0001t0002g0152 |
2 | HG02109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1297-140G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78483178 | |||||||
| chr15:78483210 | A | C | 2 | a0001c0001t0001g0033 a0001c0001t0014g0034 |
2 | NA18943.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1297-108A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 10/21 | chr15 | 78483210 | |||||||
| chr15:78483576 | T | A | 3 | a0001c0001t0007g0334 a0001c0001t0007g0336 a0001c0001t0007g0338 |
3 | NA18983.hp2 NA19084.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1413+142T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78483576 | |||||||
| chr15:78483756 | A | G | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.1413+322A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78483756 | |||||||
| chr15:78483785 | C | CT | 6 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(3): Show |
7 | HG00438.hp1 HG01169.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1413+367dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr15 | 78483785 | ||||||
| chr15:78483785 | CT | C | 16 | a0001c0001t0001g0308 a0001c0001t0002g0278 a0001c0001t0008g0026 others(13): Show |
17 | HG01496.hp1 HG03491.hp1 NA18942.hp2 others(14): Show |
intron_variant | MODIFIER | c.1413+367delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr15 | 78483785 | ||||||
| chr15:78483810 | G | A | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1413+376G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78483810 | |||||||
| chr15:78483888 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0074 |
2 | NA18949.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1413+454G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78483888 | |||||||
| chr15:78483975 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1413+541G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78483975 | |||||||
| chr15:78484007 | A | T | 1 | a0001c0006t0024g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1413+573A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78484007 | |||||||
| chr15:78484014 | A | T | 2 | a0001c0001t0020g0135 a0001c0001t0020g0136 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1413+580A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78484014 | |||||||
| chr15:78484114 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(98): Show |
113 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1414-647C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78484114 | |||||||
| chr15:78484115 | G | A | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-646G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78484115 | |||||||
| chr15:78484384 | C | T | 4 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-377C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 11/21 | chr15 | 78484384 | |||||||
| chr15:78484970 | G | A | 376 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(373): Show |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.1573+50G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | chr15 | 78484970 | |||||||
| chr15:78485015 | G | T | 4 | a0001c0001t0002g0207 a0001c0001t0002g0221 a0001c0001t0002g0222 others(1): Show |
4 | NA18952.hp2 NA18959.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1573+95G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | chr15 | 78485015 | |||||||
| chr15:78485350 | A | T | 4 | a0003c0005t0009g0126 a0003c0005t0009g0127 a0003c0005t0009g0128 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1574-355A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | chr15 | 78485350 | |||||||
| chr15:78485398 | G | T | 1 | a0001c0001t0009g0125 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1574-307G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | chr15 | 78485398 | |||||||
| chr15:78485420 | G | GA | 375 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(372): Show |
410 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(407): Show |
intron_variant | MODIFIER | c.1574-279dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr15 | 78485420 | ||||||
| chr15:78485552 | A | G | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1574-153A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 12/21 | chr15 | 78485552 | |||||||
| chr15:78485857 | G | A | 1 | a0001c0006t0025g0132 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1709+17G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78485857 | |||||||
| chr15:78485910 | C | G | 1 | a0001c0001t0002g0229 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1709+70C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78485910 | |||||||
| chr15:78486301 | G | C | 3 | a0001c0001t0046g0117 a0001c0001t0047g0122 a0001c0001t0048g0123 |
3 | HG02886.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1709+461G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486301 | |||||||
| chr15:78486335 | G | A | 1 | a0001c0001t0006g0111 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1709+495G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486335 | |||||||
| chr15:78486536 | C | T | 2 | a0001c0001t0001g0048 a0001c0002t0017g0176 |
2 | HG00639.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1709+696C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486536 | |||||||
| chr15:78486541 | G | T | 1 | a0001c0001t0033g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1709+701G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486541 | |||||||
| chr15:78486552 | C | T | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1709+712C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486552 | |||||||
| chr15:78486582 | G | A | 1 | a0001c0001t0033g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1709+742G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486582 | |||||||
| chr15:78486610 | GA | G | 9 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(6): Show |
10 | HG02109.hp2 NA18942.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1709+782delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr15 | 78486610 | ||||||
| chr15:78486611 | A | G | 169 | a0001c0001t0004g0104 a0001c0001t0007g0027 a0001c0001t0007g0321 others(166): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1709+771A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486611 | |||||||
| chr15:78486612 | A | G | 9 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(6): Show |
10 | HG02109.hp2 NA18942.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1709+772A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486612 | |||||||
| chr15:78486616 | A | G | 4 | a0003c0005t0009g0126 a0003c0005t0009g0127 a0003c0005t0009g0128 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1709+776A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486616 | |||||||
| chr15:78486630 | A | G | 178 | a0001c0001t0004g0104 a0001c0001t0007g0027 a0001c0001t0007g0321 others(175): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1709+790A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486630 | |||||||
| chr15:78486653 | A | G | 8 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(5): Show |
9 | NA18942.hp2 NA18968.hp1 NA18972.hp2 others(6): Show |
intron_variant | MODIFIER | c.1709+813A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486653 | |||||||
| chr15:78486748 | CA | C | 3 | a0001c0002t0005g0352 a0001c0002t0005g0353 a0001c0002t0037g0351 |
3 | HG00639.hp1 HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1709+909delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486748 | |||||||
| chr15:78486885 | G | A | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.1710-848G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78486885 | |||||||
| chr15:78487042 | C | T | 178 | a0001c0001t0004g0104 a0001c0001t0007g0027 a0001c0001t0007g0321 others(175): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.1710-691C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78487042 | |||||||
| chr15:78487168 | T | A | 141 | a0001c0001t0004g0104 a0001c0002t0003g0003 a0001c0002t0003g0006 others(138): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1710-565T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78487168 | |||||||
| chr15:78487192 | ACAAT | A | 355 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(352): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.1710-536_1710-533d others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr15 | 78487192 | ||||||
| chr15:78487459 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(103): Show |
118 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1710-274C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78487459 | |||||||
| chr15:78487591 | A | G | 28 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(25): Show |
29 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.1710-142A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78487591 | |||||||
| chr15:78487596 | T | C | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1710-137T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 13/21 | chr15 | 78487596 | |||||||
| chr15:78487967 | T | C | 1 | a0001c0001t0002g0215 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1794+150T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 14/21 | chr15 | 78487967 | |||||||
| chr15:78488039 | A | G | 1 | a0001c0002t0003g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1795-141A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 14/21 | chr15 | 78488039 | |||||||
| chr15:78488442 | G | A | 3 | a0001c0002t0005g0369 a0001c0002t0005g0370 a0001c0002t0005g0371 |
3 | HG00323.hp2 HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1951+106G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 15/21 | chr15 | 78488442 | |||||||
| chr15:78488817 | G | T | 4 | a0001c0002t0003g0189 a0001c0002t0003g0190 a0001c0002t0003g0191 others(1): Show |
4 | HG01069.hp2 HG01106.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.2076+46G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78488817 | |||||||
| chr15:78488909 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2076+138C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78488909 | |||||||
| chr15:78488970 | G | A | 22 | a0001c0001t0002g0148 a0001c0001t0007g0027 a0001c0001t0007g0321 others(19): Show |
22 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.2076+199G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78488970 | |||||||
| chr15:78488974 | C | A | 4 | a0001c0001t0011g0143 a0001c0001t0011g0144 a0001c0001t0011g0145 others(1): Show |
4 | HG01496.hp1 HG03486.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2076+203C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78488974 | |||||||
| chr15:78489163 | G | A | 7 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(4): Show |
10 | HG01928.hp2 HG01934.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.2076+392G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489163 | |||||||
| chr15:78489222 | C | CA | 7 | a0001c0001t0002g0227 a0001c0001t0011g0142 a0001c0001t0011g0143 others(4): Show |
7 | HG01496.hp1 HG02135.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2076+467dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr15 | 78489222 | ||||||
| chr15:78489222 | CA | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(135): Show |
151 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.2076+467delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr15 | 78489222 | ||||||
| chr15:78489282 | G | C | 1 | a0001c0001t0014g0087 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2076+511G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489282 | |||||||
| chr15:78489339 | C | T | 1 | a0001c0001t0011g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2076+568C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489339 | |||||||
| chr15:78489345 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(98): Show |
113 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.2076+574G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489345 | |||||||
| chr15:78489378 | A | C | 1 | a0001c0002t0022g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2076+607A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489378 | |||||||
| chr15:78489395 | A | C | 1 | a0001c0001t0011g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2076+624A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489395 | |||||||
| chr15:78489425 | A | G | 1 | a0001c0002t0003g0199 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2076+654A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489425 | |||||||
| chr15:78489511 | T | C | 1 | a0001c0002t0003g0158 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2076+740T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489511 | |||||||
| chr15:78489584 | C | T | 1 | a0001c0002t0004g0250 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2076+813C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489584 | |||||||
| chr15:78489647 | T | TG | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.2077-771dupG | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr15 | 78489647 | ||||||
| chr15:78489659 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2077-763C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489659 | |||||||
| chr15:78489681 | A | T | 1 | a0001c0001t0002g0280 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2077-741A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489681 | |||||||
| chr15:78489753 | C | T | 141 | a0001c0001t0004g0104 a0001c0002t0003g0003 a0001c0002t0003g0006 others(138): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2077-669C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489753 | |||||||
| chr15:78489936 | A | G | 1 | a0001c0002t0003g0183 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2077-486A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489936 | |||||||
| chr15:78489956 | T | C | 2 | a0001c0004t0001g0094 a0001c0004t0016g0095 |
2 | NA18997.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2077-466T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489956 | |||||||
| chr15:78489984 | T | G | 69 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(66): Show |
73 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(70): Show |
intron_variant | MODIFIER | c.2077-438T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78489984 | |||||||
| chr15:78490243 | A | T | 5 | a0001c0001t0001g0041 a0001c0001t0001g0063 a0001c0001t0001g0081 others(2): Show |
5 | NA18747.hp2 NA18944.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.2077-179A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78490243 | |||||||
| chr15:78490250 | A | T | 41 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0030 others(38): Show |
42 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.2077-172A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78490250 | |||||||
| chr15:78490326 | T | G | 1 | a0001c0001t0002g0279 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2077-96T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78490326 | |||||||
| chr15:78490357 | A | T | 2 | a0001c0006t0025g0131 a0001c0006t0025g0132 |
2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2077-65A>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78490357 | |||||||
| chr15:78490390 | C | T | 18 | a0001c0001t0002g0017 a0001c0001t0002g0207 a0001c0001t0002g0208 others(15): Show |
19 | HG02074.hp2 HG02083.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.2077-32C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 16/21 | chr15 | 78490390 | |||||||
| chr15:78490765 | T | C | 1 | a0001c0001t0002g0212 | 1 | NA19084.hp1 | splice_region_variant&intron_variant | LOW | c.2324+4T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78490765 | |||||||
| chr15:78490857 | A | G | 3 | a0002c0003t0010g0013 a0002c0003t0010g0139 a0002c0003t0010g0141 |
4 | HG01109.hp1 HG02257.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.2324+96A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78490857 | |||||||
| chr15:78490935 | G | A | 36 | a0001c0002t0004g0004 a0001c0002t0004g0249 a0001c0002t0005g0004 others(33): Show |
38 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.2324+174G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78490935 | |||||||
| chr15:78490952 | C | T | 1 | a0001c0002t0005g0342 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2324+191C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78490952 | |||||||
| chr15:78491106 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2324+345G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491106 | |||||||
| chr15:78491157 | A | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG03579.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2324+396A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491157 | |||||||
| chr15:78491341 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(104): Show |
119 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.2324+580C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491341 | |||||||
| chr15:78491382 | G | A | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2324+621G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491382 | |||||||
| chr15:78491470 | A | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0121 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2324+709A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491470 | |||||||
| chr15:78491490 | GTATGTAT others(5): Show |
G | 139 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(136): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.2324+743_2324+754d others(14): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78491490 | ||||||
| chr15:78491539 | C | G | 11 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0096 others(8): Show |
11 | HG00438.hp2 NA18956.hp2 NA18978.hp2 others(8): Show |
intron_variant | MODIFIER | c.2324+778C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491539 | |||||||
| chr15:78491607 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2324+846C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78491607 | |||||||
| chr15:78492036 | T | G | 5 | a0001c0001t0008g0316 a0001c0001t0008g0317 a0001c0001t0008g0318 others(2): Show |
5 | NA18942.hp2 NA18972.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.2324+1275T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492036 | |||||||
| chr15:78492256 | A | ACCCAGAT others(327): Show |
1 | a0001c0002t0012g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2324+1512_2324+151 others(338): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78492256 | ||||||
| chr15:78492362 | C | CAAAAATT others(13): Show |
205 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(202): Show |
222 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(219): Show |
intron_variant | MODIFIER | c.2325-1542_2325-152 others(24): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78492362 | ||||||
| chr15:78492409 | T | A | 4 | a0003c0005t0009g0126 a0003c0005t0009g0127 a0003c0005t0009g0128 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325-1500T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492409 | |||||||
| chr15:78492561 | A | ATTTG | 39 | a0001c0002t0004g0019 a0001c0002t0004g0020 a0001c0002t0004g0021 others(36): Show |
42 | HG00280.hp1 HG00423.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.2325-1332_2325-132 others(8): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78492561 | ||||||
| chr15:78492577 | G | T | 4 | a0001c0001t0002g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(1): Show |
4 | HG02922.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325-1332G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492577 | |||||||
| chr15:78492640 | G | T | 5 | a0001c0001t0011g0142 a0001c0001t0011g0143 a0001c0001t0011g0144 others(2): Show |
5 | HG01496.hp1 HG02818.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2325-1269G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492640 | |||||||
| chr15:78492651 | G | A | 4 | a0001c0002t0004g0022 a0001c0002t0004g0251 a0001c0002t0004g0267 others(1): Show |
4 | HG01891.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325-1258G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492651 | |||||||
| chr15:78492919 | T | C | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.2325-990T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78492919 | |||||||
| chr15:78493202 | CAGAT | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(107): Show |
122 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2325-703_2325-700d others(6): Show |
IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78493202 | ||||||
| chr15:78493460 | T | G | 67 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(64): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.2325-449T>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78493460 | |||||||
| chr15:78493602 | A | AT | 39 | a0001c0002t0004g0004 a0001c0002t0005g0004 a0001c0002t0005g0028 others(36): Show |
41 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.2325-295dupT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78493602 | ||||||
| chr15:78493602 | AT | A | 66 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(63): Show |
70 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(67): Show |
intron_variant | MODIFIER | c.2325-295delT | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr15 | 78493602 | ||||||
| chr15:78493642 | A | G | 1 | a0001c0001t0018g0326 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2325-267A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78493642 | |||||||
| chr15:78493724 | G | A | 2 | a0001c0001t0046g0117 a0001c0001t0048g0123 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2325-185G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78493724 | |||||||
| chr15:78493769 | G | T | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2325-140G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78493769 | |||||||
| chr15:78493851 | A | G | 6 | a0001c0002t0004g0261 a0001c0002t0004g0264 a0001c0002t0004g0269 others(3): Show |
6 | HG00280.hp1 HG00423.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.2325-58A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 18/21 | chr15 | 78493851 | |||||||
| chr15:78494068 | A | C | 376 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(373): Show |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.2472+12A>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 19/21 | chr15 | 78494068 | |||||||
| chr15:78494496 | T | A | 2 | a0001c0006t0025g0131 a0001c0006t0025g0132 |
2 | HG02630.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2595+232T>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494496 | |||||||
| chr15:78494501 | A | G | 10 | a0001c0002t0003g0006 a0001c0002t0003g0014 a0001c0002t0003g0156 others(7): Show |
13 | HG00544.hp2 HG00673.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.2595+237A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494501 | |||||||
| chr15:78494756 | A | G | 2 | a0001c0001t0002g0208 a0001c0001t0002g0225 |
2 | HG02074.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2595+492A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494756 | |||||||
| chr15:78494820 | G | A | 1 | a0001c0001t0033g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2595+556G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494820 | |||||||
| chr15:78494858 | C | A | 7 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 others(4): Show |
8 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2595+594C>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494858 | |||||||
| chr15:78494867 | C | T | 1 | a0001c0006t0024g0133 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2595+603C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78494867 | |||||||
| chr15:78495076 | GA | G | 9 | a0001c0001t0008g0026 a0001c0001t0008g0314 a0001c0001t0008g0315 others(6): Show |
10 | HG02109.hp2 NA18942.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.2595+814delA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr15 | 78495076 | ||||||
| chr15:78495238 | G | A | 352 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(349): Show |
382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.2595+974G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78495238 | |||||||
| chr15:78495918 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0016g0059 |
2 | HG00597.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.2596-1208T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78495918 | |||||||
| chr15:78496158 | G | C | 62 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(59): Show |
70 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.2596-968G>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496158 | |||||||
| chr15:78496231 | G | T | 4 | a0001c0001t0002g0207 a0001c0001t0002g0221 a0001c0001t0002g0222 others(1): Show |
4 | NA18952.hp2 NA18959.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.2596-895G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496231 | |||||||
| chr15:78496307 | G | T | 5 | a0002c0003t0010g0013 a0002c0003t0010g0137 a0002c0003t0010g0139 others(2): Show |
6 | HG01109.hp1 HG02257.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.2596-819G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496307 | |||||||
| chr15:78496415 | C | CA | 4 | a0001c0006t0024g0133 a0001c0006t0024g0134 a0001c0006t0025g0131 others(1): Show |
4 | HG02630.hp1 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2596-710dupA | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr15 | 78496415 | ||||||
| chr15:78496465 | A | G | 376 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(373): Show |
411 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(408): Show |
intron_variant | MODIFIER | c.2596-661A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496465 | |||||||
| chr15:78496506 | G | T | 3 | a0001c0001t0007g0334 a0001c0001t0007g0336 a0001c0001t0007g0338 |
3 | NA18983.hp2 NA19084.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2596-620G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496506 | |||||||
| chr15:78496637 | C | G | 2 | a0001c0006t0024g0133 a0001c0006t0024g0134 |
2 | HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2596-489C>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496637 | |||||||
| chr15:78496722 | G | T | 3 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0043g0294 |
3 | HG01978.hp2 HG02004.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2596-404G>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496722 | |||||||
| chr15:78496784 | A | G | 3 | a0001c0001t0009g0012 a0001c0001t0009g0124 a0001c0001t0009g0125 |
4 | HG02451.hp1 HG02615.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.2596-342A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496784 | |||||||
| chr15:78496849 | G | A | 28 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(25): Show |
29 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.2596-277G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496849 | |||||||
| chr15:78496881 | G | A | 140 | a0001c0002t0003g0003 a0001c0002t0003g0006 a0001c0002t0003g0014 others(137): Show |
153 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2596-245G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496881 | |||||||
| chr15:78496921 | C | T | 1 | a0001c0001t0011g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2596-205C>T | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 20/21 | chr15 | 78496921 | |||||||
| chr15:78497330 | A | G | 21 | a0001c0001t0007g0027 a0001c0001t0007g0321 a0001c0001t0007g0322 others(18): Show |
21 | HG00408.hp2 HG02074.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.2781+19A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/21 | chr15 | 78497330 | |||||||
| chr15:78497334 | T | C | 67 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0024 others(64): Show |
71 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(68): Show |
intron_variant | MODIFIER | c.2781+23T>C | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/21 | chr15 | 78497334 | |||||||
| chr15:78497420 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2781+109A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/21 | chr15 | 78497420 | |||||||
| chr15:78497759 | G | A | 360 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(357): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.2782-274G>A | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/21 | chr15 | 78497759 | |||||||
| chr15:78497847 | A | G | 34 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0030 others(31): Show |
36 | HG00738.hp2 HG00741.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.2782-186A>G | IREB2 | ENSG00000136381.13 | transcript | ENST00000258886.13 | protein_coding | 21/21 | chr15 | 78497847 |