Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79621 |
| ensemblid | ENSG00000136104.21 |
| hgncid | 25671 |
| symbol | RNASEH2B |
| name | ribonuclease H2 subunit B |
| refseq_nuc | NM_024570.4 |
| refseq_prot | NP_078846.2 |
| ensembl_nuc | ENST00000336617.8 |
| ensembl_prot | ENSP00000337623.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 50909791 |
| end | 50956762 |
| strand | + |
| ver | v1.2 |
| region | chr13:50909791-50956762 |
| region5000 | chr13:50904791-50961762 |
| regionname0 | RNASEH2B_chr13_50909791_50956762 |
| regionname5000 | RNASEH2B_chr13_50904791_50961762 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 312 | 369 | 88 | 74 | 163 | 10 | 32 | 135 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | MAAGV others(307): Show |
chr13 | 50904791 | 50961762 |
| a0002 | 0/0 | 312 | 11 | 7 | 0 | 0 | 0 | 4 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | MAAGV others(307): Show |
chr13 | 50904791 | 50961762 |
| a0003 | 0/0 | 312 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | MAAGV others(307): Show |
chr13 | 50904791 | 50961762 |
| a0004 | 0/0 | 312 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | MATGV others(307): Show |
chr13 | 50904791 | 50961762 |
| a0005 | 0/0 | 312 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | MAAGV others(307): Show |
chr13 | 50904791 | 50961762 |
| a0006 | 0/0 | 312 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | MAAGV others(307): Show |
chr13 | 50904791 | 50961762 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 936 | 359 | 78 | 74 | 163 | 10 | 32 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ATGGC others(931): Show |
chr13 | 50904791 | 50961762 | ||
| a0001c0003 | 0/0 | 936 | 5 | 5 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ATGGC others(931): Show |
chr13 | 50904791 | 50961762 | ||
| a0001c0004 | 0/0 | 936 | 5 | 5 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ATGGC others(931): Show |
chr13 | 50904791 | 50961762 | ||
| a0002c0002 | 0/0 | 937 | 11 | 7 | 0 | 0 | 0 | 4 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ATGGC others(932): Show |
chr13 | 50904791 | 50961762 | ||
| a0003c0006 | 0/0 | 936 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ATGGC others(931): Show |
chr13 | 50904791 | 50961762 | ||
| a0004c0005 | 0/0 | 936 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ATGGC others(931): Show |
chr13 | 50904791 | 50961762 | ||
| a0005c0007 | 0/0 | 936 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ATGGC others(931): Show |
chr13 | 50904791 | 50961762 | ||
| a0006c0008 | 0/0 | 936 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ATGGC others(931): Show |
chr13 | 50904791 | 50961762 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1513 | 358 | 77 | 74 | 163 | 10 | 32 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ACTAG others(1508): Show |
chr13 | 50904791 | 50961762 |
| a0001c0001t0003 | 0/0 | 1513 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ACTAG others(1508): Show |
chr13 | 50904791 | 50961762 |
| a0001c0003t0001 | 0/0 | 1513 | 5 | 5 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ACTAG others(1508): Show |
chr13 | 50904791 | 50961762 |
| a0001c0004t0001 | 0/0 | 1513 | 5 | 5 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ACTAG others(1508): Show |
chr13 | 50904791 | 50961762 |
| a0002c0002t0002 | 0/0 | 1514 | 11 | 7 | 0 | 0 | 0 | 4 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ACTAG others(1509): Show |
chr13 | 50904791 | 50961762 |
| a0003c0006t0001 | 0/0 | 1513 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ACTAG others(1508): Show |
chr13 | 50904791 | 50961762 |
| a0004c0005t0001 | 0/0 | 1513 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ACTAG others(1508): Show |
chr13 | 50904791 | 50961762 |
| a0005c0007t0001 | 0/0 | 1513 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ACTAG others(1508): Show |
chr13 | 50904791 | 50961762 |
| a0006c0008t0001 | 0/0 | 1513 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | ACTAG others(1508): Show |
chr13 | 50904791 | 50961762 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 2 | 7 | 2 | 2 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0002 | 0/0 | 12 | 0 | 7 | 3 | 0 | 2 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0003 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0006 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0007 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0011 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0012 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0022 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0118 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0003t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0004t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0001c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0002c0002t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0002c0002t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0002c0002t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0003c0006t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0004c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0005c0007t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| a0006c0008t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | GBR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | IBS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0122 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0045 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0105 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0037 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0165 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0202 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0045 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0037 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0053 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03139 | hp2 | a0003 | c0006 | t0001 | g0139 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03225 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03453 | hp2 | a0001 | c0004 | t0001 | g0166 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0124 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03516 | hp2 | a0001 | c0004 | t0001 | g0164 | AFR | ESN | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0201 | AFR | GWD | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0103 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03710 | hp2 | a0004 | c0005 | t0001 | g0013 | SAS | PJL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03942 | hp2 | a0005 | c0007 | t0001 | g0095 | SAS | BEB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0123 | AFR | YRI | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | YRI | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19000 | hp1 | a0006 | c0008 | t0001 | g0091 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ASW | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | GIH | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0053 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0200 | AFR | USA | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | USA | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | USA | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0078 | REF | REF | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0118 | REF | REF | RNASEH2B_chr13_50904791_50961762 | RNASEH2B | chr13 | 50904791 | 50961762 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:50910083 | G | A | 1 | a0004 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.7G>A | p.Ala3Thr | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/11 | 293/1513 | 7/939 | 3/312 | chr13 | 50910083 | |||
| chr13:50945439 | G | A | 1 | a0003 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.523G>A | p.Val175Met | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/11 | 809/1513 | 523/939 | 175/312 | chr13 | 50945439 | |||
| chr13:50956394 | G | T | 1 | a0006 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.859G>T | p.Ala287Ser | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 11/11 | 1145/1513 | 859/939 | 287/312 | chr13 | 50956394 | |||
| chr13:50956430 | A | G | 1 | a0005 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.895A>G | p.Thr299Ala | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 11/11 | 1181/1513 | 895/939 | 299/312 | chr13 | 50956430 | |||
| chr13:50956450 | T | TA | 1 | a0002 | 11 | HG02055.hp2 HG02559.hp1 HG02698.hp1 others(8): Show |
frameshift_variant | HIGH | c.925dupA | p.Ile309fs | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 11/11 | 1212/1513 | 926/939 | 309/312 | INFO_REALIGN_3_PRIME | chr13 | 50956450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:50929494 | G | A | 1 | a0001c0003 | 5 | HG02109.hp2 HG02895.hp1 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.156G>A | p.Leu52Leu | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 3/11 | 442/1513 | 156/939 | 52/312 | chr13 | 50929494 | |||
| chr13:50929527 | A | G | 1 | a0001c0004 | 5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
synonymous_variant | LOW | c.189A>G | p.Val63Val | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 3/11 | 475/1513 | 189/939 | 63/312 | chr13 | 50929527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:50909867 | G | C | 1 | a0002c0002t0002 | 11 | HG02055.hp2 HG02559.hp1 HG02698.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-210G>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/11 | 210 | chr13 | 50909867 | ||||||
| chr13:50956720 | A | G | 1 | a0001c0001t0003 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*246A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 11/11 | 246 | chr13 | 50956720 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:50910220 | C | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
221 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.64+80C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50910220 | |||||||
| chr13:50910278 | G | T | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.64+138G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50910278 | |||||||
| chr13:50910309 | C | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
215 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.64+169C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50910309 | |||||||
| chr13:50910481 | A | T | 15 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0236 others(12): Show |
18 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+341A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50910481 | |||||||
| chr13:50910551 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64+411C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50910551 | |||||||
| chr13:50910672 | G | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | NA19010.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.64+532G>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50910672 | |||||||
| chr13:50910959 | A | G | 8 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(5): Show |
8 | HG01891.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+819A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50910959 | |||||||
| chr13:50911110 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64+970C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50911110 | |||||||
| chr13:50911563 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0209 others(17): Show |
32 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.64+1423A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50911563 | |||||||
| chr13:50911904 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.64+1764T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50911904 | |||||||
| chr13:50911980 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(35): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.64+1840G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50911980 | |||||||
| chr13:50912031 | G | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+1891G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50912031 | |||||||
| chr13:50912058 | C | G | 5 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0122 others(2): Show |
7 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.64+1918C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50912058 | |||||||
| chr13:50912067 | A | G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(63): Show |
108 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.64+1927A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50912067 | |||||||
| chr13:50912214 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
4 | HG02258.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+2074C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50912214 | |||||||
| chr13:50912568 | A | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+2428A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50912568 | |||||||
| chr13:50912607 | C | T | 3 | a0002c0002t0002g0042 a0002c0002t0002g0123 a0002c0002t0002g0124 |
4 | HG02559.hp1 HG02965.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.64+2467C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50912607 | |||||||
| chr13:50912776 | A | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+2636A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50912776 | |||||||
| chr13:50912916 | A | T | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64+2776A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50912916 | |||||||
| chr13:50913149 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64+3009T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50913149 | |||||||
| chr13:50913206 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(35): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.64+3066G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50913206 | |||||||
| chr13:50913214 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.64+3074T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50913214 | |||||||
| chr13:50913227 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.64+3087C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50913227 | |||||||
| chr13:50913421 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.64+3281G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50913421 | |||||||
| chr13:50913488 | GA | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
8 | HG01256.hp2 HG02027.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+3361delA | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50913488 | ||||||
| chr13:50913499 | A | G | 26 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0049 others(23): Show |
33 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.64+3359A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50913499 | |||||||
| chr13:50913570 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64+3430C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50913570 | |||||||
| chr13:50913696 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.64+3556A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50913696 | |||||||
| chr13:50913745 | T | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0209 others(17): Show |
32 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.64+3605T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50913745 | |||||||
| chr13:50913848 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.64+3708T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50913848 | |||||||
| chr13:50914043 | AT | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
165 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.64+3921delT | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50914043 | ||||||
| chr13:50914043 | ATT | A | 140 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(137): Show |
210 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.64+3920_64+3921del others(2): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50914043 | ||||||
| chr13:50914200 | C | T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG02109.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.64+4060C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50914200 | |||||||
| chr13:50914466 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.64+4326G>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50914466 | |||||||
| chr13:50914543 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.64+4403A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50914543 | |||||||
| chr13:50914582 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.64+4442C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50914582 | |||||||
| chr13:50914636 | A | G | 1 | a0001c0001t0001g0114 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.64+4496A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50914636 | |||||||
| chr13:50914802 | A | C | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.64+4662A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50914802 | |||||||
| chr13:50914814 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+4674G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50914814 | |||||||
| chr13:50914985 | G | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0046 others(12): Show |
23 | HG01074.hp1 HG01106.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.64+4845G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50914985 | |||||||
| chr13:50915002 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.64+4862G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50915002 | |||||||
| chr13:50915050 | G | A | 29 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0049 others(26): Show |
36 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.64+4910G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50915050 | |||||||
| chr13:50915107 | T | C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0236 others(12): Show |
18 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+4967T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50915107 | |||||||
| chr13:50915209 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.64+5069A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50915209 | |||||||
| chr13:50915458 | C | T | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.64+5318C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50915458 | |||||||
| chr13:50915618 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.64+5478C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50915618 | |||||||
| chr13:50915685 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.64+5545C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50915685 | |||||||
| chr13:50915772 | C | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0174 others(5): Show |
13 | HG01074.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.64+5632C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50915772 | |||||||
| chr13:50916060 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
224 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.64+5920T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50916060 | |||||||
| chr13:50916076 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.64+5936A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50916076 | |||||||
| chr13:50916276 | A | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.64+6136A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50916276 | |||||||
| chr13:50916338 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0107 a0001c0001t0001g0108 others(6): Show |
11 | HG00673.hp1 HG02027.hp2 NA18961.hp1 others(8): Show |
intron_variant | MODIFIER | c.64+6198C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50916338 | |||||||
| chr13:50916423 | C | G | 1 | a0001c0001t0001g0006 | 7 | HG01243.hp1 HG02451.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.64+6283C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50916423 | |||||||
| chr13:50916495 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.64+6355T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50916495 | |||||||
| chr13:50917073 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(49): Show |
73 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.64+6933C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917073 | |||||||
| chr13:50917086 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.64+6946C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917086 | |||||||
| chr13:50917169 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.64+7029A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917169 | |||||||
| chr13:50917195 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.64+7055G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917195 | |||||||
| chr13:50917209 | A | G | 1 | a0002c0002t0002g0105 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64+7069A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917209 | |||||||
| chr13:50917252 | C | T | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+7112C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917252 | |||||||
| chr13:50917260 | C | A | 1 | a0001c0001t0001g0061 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.64+7120C>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917260 | |||||||
| chr13:50917270 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.64+7130C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917270 | |||||||
| chr13:50917287 | G | T | 1 | a0001c0001t0001g0038 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.64+7147G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917287 | |||||||
| chr13:50917644 | G | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(148): Show |
224 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(221): Show |
intron_variant | MODIFIER | c.64+7504G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917644 | |||||||
| chr13:50917707 | C | G | 1 | a0001c0001t0001g0223 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.64+7567C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917707 | |||||||
| chr13:50917776 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+7636G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917776 | |||||||
| chr13:50917826 | A | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
227 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(224): Show |
intron_variant | MODIFIER | c.64+7686A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917826 | |||||||
| chr13:50917946 | C | T | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+7806C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917946 | |||||||
| chr13:50917957 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.64+7817C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50917957 | |||||||
| chr13:50918001 | C | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | NA18950.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.64+7861C>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918001 | |||||||
| chr13:50918009 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.64+7869T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918009 | |||||||
| chr13:50918101 | A | G | 53 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(50): Show |
75 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.64+7961A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918101 | |||||||
| chr13:50918176 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02148.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.64+8036C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918176 | |||||||
| chr13:50918238 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0203 |
5 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.64+8098C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918238 | |||||||
| chr13:50918339 | G | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0181 others(4): Show |
10 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+8199G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918339 | |||||||
| chr13:50918366 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.64+8226T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918366 | |||||||
| chr13:50918380 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.64+8240G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918380 | |||||||
| chr13:50918389 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.64+8249G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918389 | |||||||
| chr13:50918429 | G | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0016 others(16): Show |
34 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.64+8289G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918429 | |||||||
| chr13:50918433 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.64+8293G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918433 | |||||||
| chr13:50918768 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64+8628A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50918768 | |||||||
| chr13:50919142 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.65-8265T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50919142 | |||||||
| chr13:50919298 | A | G | 4 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG01891.hp1 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-8109A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50919298 | |||||||
| chr13:50919368 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0102 |
5 | HG01070.hp1 HG01071.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-8039A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50919368 | |||||||
| chr13:50919695 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0016 others(16): Show |
34 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.65-7712C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50919695 | |||||||
| chr13:50919899 | T | A | 1 | a0001c0001t0001g0063 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.65-7508T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50919899 | |||||||
| chr13:50919940 | C | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01070.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.65-7467C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50919940 | |||||||
| chr13:50920007 | G | GTGTTT | 11 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(8): Show |
11 | HG01070.hp2 HG01123.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.65-7357_65-7353dup others(5): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50920007 | ||||||
| chr13:50920007 | G | GTGTTTTG others(3): Show |
6 | a0001c0001t0001g0054 a0001c0001t0001g0120 a0001c0001t0001g0231 others(3): Show |
8 | HG02027.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.65-7362_65-7353dup others(10): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50920007 | ||||||
| chr13:50920007 | GTGTTT | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0011 others(65): Show |
107 | HG00099.hp1 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.65-7357_65-7353del others(5): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50920007 | ||||||
| chr13:50920007 | GTGTTTTG others(3): Show |
G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0052 a0001c0001t0001g0068 others(5): Show |
13 | HG01884.hp1 HG01884.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-7362_65-7353del others(10): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50920007 | ||||||
| chr13:50920007 | GTGTTTTG others(8): Show |
G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
6 | HG01515.hp1 NA18939.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.65-7367_65-7353del others(15): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50920007 | ||||||
| chr13:50920007 | GTGTTTTG others(13): Show |
G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0183 others(2): Show |
7 | HG01109.hp1 HG02145.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.65-7372_65-7353del others(20): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50920007 | ||||||
| chr13:50920351 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0209 others(17): Show |
32 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.65-7056G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50920351 | |||||||
| chr13:50920366 | G | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG02280.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.65-7041G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50920366 | |||||||
| chr13:50920638 | A | C | 1 | a0001c0001t0001g0155 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.65-6769A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50920638 | |||||||
| chr13:50920709 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.65-6698G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50920709 | |||||||
| chr13:50920851 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(46): Show |
70 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(67): Show |
intron_variant | MODIFIER | c.65-6556A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50920851 | |||||||
| chr13:50921042 | C | T | 4 | a0001c0003t0001g0053 a0001c0003t0001g0200 a0001c0003t0001g0201 others(1): Show |
5 | HG02109.hp2 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-6365C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50921042 | |||||||
| chr13:50921191 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.65-6216C>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50921191 | |||||||
| chr13:50921824 | T | G | 1 | a0001c0001t0001g0115 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.65-5583T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50921824 | |||||||
| chr13:50922013 | C | T | 4 | a0001c0001t0001g0050 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
5 | HG01109.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-5394C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922013 | |||||||
| chr13:50922184 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
225 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.65-5223G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922184 | |||||||
| chr13:50922215 | C | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0181 others(4): Show |
10 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-5192C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922215 | |||||||
| chr13:50922216 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0075 |
2 | NA18951.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.65-5191G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922216 | |||||||
| chr13:50922421 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.65-4986T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922421 | |||||||
| chr13:50922432 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.65-4975G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922432 | |||||||
| chr13:50922452 | A | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0055 others(24): Show |
40 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.65-4955A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922452 | |||||||
| chr13:50922467 | C | T | 4 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG01891.hp1 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-4940C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922467 | |||||||
| chr13:50922472 | A | G | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.65-4935A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922472 | |||||||
| chr13:50922659 | A | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0181 others(4): Show |
10 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-4748A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922659 | |||||||
| chr13:50922687 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0167 others(20): Show |
35 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.65-4720G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922687 | |||||||
| chr13:50922835 | G | C | 4 | a0001c0003t0001g0053 a0001c0003t0001g0200 a0001c0003t0001g0201 others(1): Show |
5 | HG02109.hp2 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-4572G>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50922835 | |||||||
| chr13:50923007 | C | G | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-4400C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50923007 | |||||||
| chr13:50923225 | A | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.65-4182A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50923225 | |||||||
| chr13:50923488 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01070.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.65-3919T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50923488 | |||||||
| chr13:50923538 | G | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01070.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.65-3869G>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50923538 | |||||||
| chr13:50923659 | C | G | 1 | a0005c0007t0001g0095 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.65-3748C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50923659 | |||||||
| chr13:50923837 | A | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(35): Show |
62 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.65-3570A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50923837 | |||||||
| chr13:50923936 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.65-3471T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50923936 | |||||||
| chr13:50923997 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02135.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.65-3410C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50923997 | |||||||
| chr13:50924174 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.65-3233C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50924174 | |||||||
| chr13:50924188 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.65-3219A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50924188 | |||||||
| chr13:50924233 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65-3174T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50924233 | |||||||
| chr13:50924453 | A | C | 1 | a0001c0001t0001g0116 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.65-2954A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50924453 | |||||||
| chr13:50924517 | C | G | 1 | a0001c0001t0001g0121 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.65-2890C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50924517 | |||||||
| chr13:50924602 | A | G | 1 | a0001c0001t0001g0154 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.65-2805A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50924602 | |||||||
| chr13:50924699 | C | T | 1 | a0001c0001t0001g0052 | 2 | NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.65-2708C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50924699 | |||||||
| chr13:50924828 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.65-2579T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50924828 | |||||||
| chr13:50924834 | A | T | 1 | a0001c0004t0001g0166 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.65-2573A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50924834 | |||||||
| chr13:50924897 | T | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.65-2510T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50924897 | |||||||
| chr13:50925061 | G | A | 7 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0181 others(4): Show |
10 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.65-2346G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50925061 | |||||||
| chr13:50925079 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.65-2328T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50925079 | |||||||
| chr13:50925136 | T | G | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0049 others(22): Show |
32 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.65-2271T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50925136 | |||||||
| chr13:50925212 | AT | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0016 others(16): Show |
34 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.65-2185delT | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50925212 | ||||||
| chr13:50925250 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.65-2157G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50925250 | |||||||
| chr13:50925556 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.65-1851T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50925556 | |||||||
| chr13:50925560 | G | A | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.65-1847G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50925560 | |||||||
| chr13:50926065 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.65-1342C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926065 | |||||||
| chr13:50926082 | TTTG | T | 8 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0174 others(5): Show |
13 | HG01074.hp1 HG01106.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.65-1310_65-1308del others(3): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50926082 | ||||||
| chr13:50926155 | ATT | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(79): Show |
112 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.65-1243_65-1242del others(2): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50926155 | ||||||
| chr13:50926158 | T | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(79): Show |
112 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.65-1249T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926158 | |||||||
| chr13:50926209 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0155 a0003c0006t0001g0139 |
3 | HG02486.hp2 HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.65-1198G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926209 | |||||||
| chr13:50926281 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.65-1126G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926281 | |||||||
| chr13:50926402 | A | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
5 | HG01109.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-1005A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926402 | |||||||
| chr13:50926434 | A | C | 4 | a0001c0003t0001g0053 a0001c0003t0001g0200 a0001c0003t0001g0201 others(1): Show |
5 | HG02109.hp2 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-973A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926434 | |||||||
| chr13:50926440 | G | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(79): Show |
112 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(109): Show |
intron_variant | MODIFIER | c.65-967G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926440 | |||||||
| chr13:50926555 | G | A | 14 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0236 others(11): Show |
17 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.65-852G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926555 | |||||||
| chr13:50926719 | A | C | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.65-688A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926719 | |||||||
| chr13:50926751 | G | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(152): Show |
229 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.65-656G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926751 | |||||||
| chr13:50926835 | T | TAAAA | 85 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(82): Show |
116 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.65-566_65-563dupAA others(2): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr13 | 50926835 | ||||||
| chr13:50926906 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0167 others(20): Show |
35 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.65-501T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926906 | |||||||
| chr13:50926934 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.65-473A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50926934 | |||||||
| chr13:50927027 | T | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.65-380T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50927027 | |||||||
| chr13:50927040 | T | C | 4 | a0001c0003t0001g0053 a0001c0003t0001g0200 a0001c0003t0001g0201 others(1): Show |
5 | HG02109.hp2 HG02895.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.65-367T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50927040 | |||||||
| chr13:50927271 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.65-136A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 1/10 | chr13 | 50927271 | |||||||
| chr13:50927657 | A | C | 4 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG01891.hp1 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+179A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50927657 | |||||||
| chr13:50927714 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.136+236A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50927714 | |||||||
| chr13:50927749 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.136+271T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50927749 | |||||||
| chr13:50927750 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.136+272C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50927750 | |||||||
| chr13:50927842 | A | G | 3 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 |
4 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+364A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50927842 | |||||||
| chr13:50927872 | A | G | 4 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG01891.hp1 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+394A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50927872 | |||||||
| chr13:50927887 | G | A | 3 | a0001c0003t0001g0053 a0001c0003t0001g0201 a0001c0003t0001g0202 |
4 | HG02109.hp2 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+409G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50927887 | |||||||
| chr13:50927904 | C | G | 4 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG01891.hp1 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+426C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50927904 | |||||||
| chr13:50928003 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.136+525A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50928003 | |||||||
| chr13:50928206 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.136+728G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50928206 | |||||||
| chr13:50928456 | A | T | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.136+978A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50928456 | |||||||
| chr13:50928457 | A | C | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.136+979A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50928457 | |||||||
| chr13:50928473 | G | A | 1 | a0001c0001t0001g0008 | 5 | HG01884.hp1 HG02717.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.136+995G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50928473 | |||||||
| chr13:50928643 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.137-832T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50928643 | |||||||
| chr13:50928802 | G | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG02280.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.137-673G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50928802 | |||||||
| chr13:50928862 | T | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0024 others(31): Show |
47 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.137-613T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50928862 | |||||||
| chr13:50928863 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.137-612T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50928863 | |||||||
| chr13:50928932 | C | CT | 41 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0044 others(38): Show |
52 | HG00639.hp2 HG00735.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.137-519dupT | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr13 | 50928932 | ||||||
| chr13:50928932 | C | CTT | 5 | a0001c0001t0001g0023 a0001c0001t0001g0187 a0001c0001t0001g0188 others(2): Show |
7 | HG01123.hp2 HG01975.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.137-520_137-519dup others(2): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr13 | 50928932 | ||||||
| chr13:50928932 | CT | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0173 others(7): Show |
19 | HG01243.hp1 HG01256.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.137-519delT | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr13 | 50928932 | ||||||
| chr13:50929225 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.137-250G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | chr13 | 50929225 | |||||||
| chr13:50929424 | T | TTGTG | 5 | a0001c0001t0003g0235 a0001c0004t0001g0045 a0001c0004t0001g0164 others(2): Show |
6 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-40_137-37dupTG others(2): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr13 | 50929424 | ||||||
| chr13:50929712 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0113 |
2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.244+130G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 3/10 | chr13 | 50929712 | |||||||
| chr13:50930130 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(44): Show |
67 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.244+548G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 3/10 | chr13 | 50930130 | |||||||
| chr13:50930336 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.245-347G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 3/10 | chr13 | 50930336 | |||||||
| chr13:50930455 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.245-228G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 3/10 | chr13 | 50930455 | |||||||
| chr13:50930648 | C | T | 6 | a0001c0001t0001g0163 a0001c0001t0001g0227 a0001c0001t0001g0231 others(3): Show |
6 | HG01891.hp1 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-35C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 3/10 | chr13 | 50930648 | |||||||
| chr13:50930659 | C | T | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.245-24C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 3/10 | chr13 | 50930659 | |||||||
| chr13:50930777 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.321+18A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50930777 | |||||||
| chr13:50930866 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.321+107A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50930866 | |||||||
| chr13:50930872 | T | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(68): Show |
118 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.321+113T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50930872 | |||||||
| chr13:50931169 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+410C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50931169 | |||||||
| chr13:50931170 | G | A | 5 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0122 others(2): Show |
7 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.321+411G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50931170 | |||||||
| chr13:50931493 | C | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(45): Show |
69 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.321+734C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50931493 | |||||||
| chr13:50931548 | T | C | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+789T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50931548 | |||||||
| chr13:50931645 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.321+886G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50931645 | |||||||
| chr13:50931737 | A | T | 1 | a0001c0001t0001g0233 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.321+978A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50931737 | |||||||
| chr13:50931927 | A | G | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.321+1168A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50931927 | |||||||
| chr13:50931955 | T | TAC | 11 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0083 others(8): Show |
12 | HG02040.hp2 HG02145.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.321+1223_321+1224d others(4): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr13 | 50931955 | ||||||
| chr13:50931955 | T | TACAC | 61 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0011 others(58): Show |
95 | HG00597.hp1 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.321+1221_321+1224d others(6): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr13 | 50931955 | ||||||
| chr13:50931955 | T | TACACAC | 12 | a0001c0001t0001g0043 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
16 | HG01515.hp2 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.321+1219_321+1224d others(8): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr13 | 50931955 | ||||||
| chr13:50931955 | T | TACACACA others(3): Show |
28 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0052 others(25): Show |
36 | HG00099.hp1 HG00639.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.321+1215_321+1224d others(12): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr13 | 50931955 | ||||||
| chr13:50931955 | T | TACACACA others(5): Show |
25 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(22): Show |
43 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.321+1213_321+1224d others(14): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr13 | 50931955 | ||||||
| chr13:50931955 | T | TACACACA others(7): Show |
10 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0133 others(7): Show |
21 | HG00609.hp1 HG02523.hp1 NA18940.hp1 others(18): Show |
intron_variant | MODIFIER | c.321+1211_321+1224d others(16): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr13 | 50931955 | ||||||
| chr13:50931955 | T | TACACACA others(9): Show |
5 | a0001c0001t0001g0132 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
5 | HG02040.hp1 HG02071.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.321+1209_321+1224d others(18): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr13 | 50931955 | ||||||
| chr13:50931955 | TAC | T | 9 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0126 others(6): Show |
13 | HG02055.hp2 HG02258.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+1223_321+1224d others(4): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr13 | 50931955 | ||||||
| chr13:50931968 | A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0152 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.321+1210_321+1222d others(15): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr13 | 50931968 | ||||||
| chr13:50932133 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.321+1374C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50932133 | |||||||
| chr13:50932156 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0084 others(21): Show |
36 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.321+1397G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50932156 | |||||||
| chr13:50932246 | T | G | 4 | a0001c0001t0001g0050 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
5 | HG01109.hp1 HG02145.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.321+1487T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50932246 | |||||||
| chr13:50932328 | T | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0016 others(20): Show |
40 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.321+1569T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50932328 | |||||||
| chr13:50932461 | C | T | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+1702C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50932461 | |||||||
| chr13:50932600 | G | A | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+1841G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50932600 | |||||||
| chr13:50933056 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.322-1829G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50933056 | |||||||
| chr13:50933093 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.322-1792A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50933093 | |||||||
| chr13:50933098 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0052 a0001c0001t0001g0054 others(1): Show |
7 | HG02280.hp1 HG02818.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.322-1787C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50933098 | |||||||
| chr13:50933473 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.322-1412G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50933473 | |||||||
| chr13:50933580 | A | C | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.322-1305A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50933580 | |||||||
| chr13:50933662 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.322-1223G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50933662 | |||||||
| chr13:50934300 | G | T | 1 | a0001c0001t0001g0025 | 2 | NA18950.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.322-585G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50934300 | |||||||
| chr13:50934421 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0096 |
3 | NA18942.hp2 NA19077.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.322-464C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50934421 | |||||||
| chr13:50934668 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.322-217T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50934668 | |||||||
| chr13:50934725 | C | A | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.322-160C>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50934725 | |||||||
| chr13:50934824 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.322-61C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50934824 | |||||||
| chr13:50934831 | T | G | 8 | a0002c0002t0002g0037 a0002c0002t0002g0041 a0002c0002t0002g0042 others(5): Show |
11 | HG02055.hp2 HG02559.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.322-54T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50934831 | |||||||
| chr13:50934841 | T | C | 1 | a0002c0002t0002g0103 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.322-44T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 4/10 | chr13 | 50934841 | |||||||
| chr13:50935331 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.436+332G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50935331 | |||||||
| chr13:50935349 | T | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0181 others(4): Show |
10 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+350T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50935349 | |||||||
| chr13:50935665 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.436+666G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50935665 | |||||||
| chr13:50935762 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.436+763G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50935762 | |||||||
| chr13:50935853 | A | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(37): Show |
69 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.436+854A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50935853 | |||||||
| chr13:50936013 | G | A | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.436+1014G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50936013 | |||||||
| chr13:50936125 | G | T | 1 | a0001c0003t0001g0201 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.436+1126G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50936125 | |||||||
| chr13:50936523 | G | C | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+1524G>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50936523 | |||||||
| chr13:50936683 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.436+1684A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50936683 | |||||||
| chr13:50936866 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.436+1867C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50936866 | |||||||
| chr13:50936981 | ATTAGCCT | A | 5 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0122 others(2): Show |
7 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+1986_436+1992d others(9): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr13 | 50936981 | ||||||
| chr13:50936995 | T | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0016 others(19): Show |
39 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.436+1996T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50936995 | |||||||
| chr13:50937206 | ATTTTTAT others(7): Show |
A | 8 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
10 | HG02055.hp2 HG02559.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+2228_436+2241d others(16): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr13 | 50937206 | ||||||
| chr13:50937212 | ATTTTTAT others(3): Show |
A | 3 | a0002c0002t0002g0037 a0002c0002t0002g0103 a0002c0002t0002g0105 |
4 | HG02698.hp1 HG02698.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+2217_436+2226d others(12): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr13 | 50937212 | ||||||
| chr13:50937265 | A | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(53): Show |
79 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.436+2266A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50937265 | |||||||
| chr13:50937291 | G | A | 5 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0122 others(2): Show |
7 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+2292G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50937291 | |||||||
| chr13:50937366 | C | T | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
225 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(222): Show |
intron_variant | MODIFIER | c.436+2367C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50937366 | |||||||
| chr13:50937480 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG01884.hp2 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.436+2481G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50937480 | |||||||
| chr13:50937559 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.436+2560G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50937559 | |||||||
| chr13:50937638 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.436+2639G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50937638 | |||||||
| chr13:50937834 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.436+2835A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50937834 | |||||||
| chr13:50937864 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0214 |
3 | HG00597.hp1 NA18944.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.436+2865T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50937864 | |||||||
| chr13:50937877 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.436+2878C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50937877 | |||||||
| chr13:50938006 | T | C | 1 | a0001c0001t0001g0046 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.436+3007T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50938006 | |||||||
| chr13:50938012 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.436+3013A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50938012 | |||||||
| chr13:50938405 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
4 | HG02258.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.436+3406C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50938405 | |||||||
| chr13:50938500 | TA | T | 7 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.436+3503delA | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr13 | 50938500 | ||||||
| chr13:50939022 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(104): Show |
153 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.436+4023A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939022 | |||||||
| chr13:50939170 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.437-4151C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939170 | |||||||
| chr13:50939289 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0076 |
3 | HG01261.hp1 HG01952.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.437-4032A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939289 | |||||||
| chr13:50939306 | A | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0155 a0003c0006t0001g0139 |
3 | HG02486.hp2 HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.437-4015A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939306 | |||||||
| chr13:50939335 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.437-3986T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939335 | |||||||
| chr13:50939356 | C | CAAAAAAA others(3): Show |
148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(145): Show |
223 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(220): Show |
intron_variant | MODIFIER | c.437-3961_437-3960i others(12): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr13 | 50939356 | ||||||
| chr13:50939356 | C | CAAAAAAA others(4): Show |
5 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0122 others(2): Show |
7 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-3961_437-3960i others(13): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr13 | 50939356 | ||||||
| chr13:50939397 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(116): Show |
182 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(179): Show |
intron_variant | MODIFIER | c.437-3924A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939397 | |||||||
| chr13:50939409 | A | G | 1 | a0001c0001t0001g0014 | 4 | HG01192.hp2 HG02622.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-3912A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939409 | |||||||
| chr13:50939441 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
6 | HG01069.hp1 HG02683.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.437-3880G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939441 | |||||||
| chr13:50939634 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0064 a0001c0001t0001g0066 others(1): Show |
5 | HG01515.hp1 NA18939.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-3687A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939634 | |||||||
| chr13:50939656 | T | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0181 others(4): Show |
10 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.437-3665T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939656 | |||||||
| chr13:50939724 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0198 a0001c0001t0001g0206 |
7 | HG01081.hp1 HG01109.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-3597A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939724 | |||||||
| chr13:50939902 | T | C | 5 | a0001c0001t0001g0227 a0001c0001t0001g0231 a0001c0001t0001g0232 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.437-3419T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50939902 | |||||||
| chr13:50940098 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0209 others(17): Show |
32 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.437-3223A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50940098 | |||||||
| chr13:50940112 | G | A | 5 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0122 others(2): Show |
7 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-3209G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50940112 | |||||||
| chr13:50940343 | T | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(130): Show |
205 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(202): Show |
intron_variant | MODIFIER | c.437-2978T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50940343 | |||||||
| chr13:50940385 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.437-2936C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50940385 | |||||||
| chr13:50940695 | C | T | 15 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0236 others(12): Show |
18 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.437-2626C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50940695 | |||||||
| chr13:50940941 | T | C | 22 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0016 others(19): Show |
39 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.437-2380T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50940941 | |||||||
| chr13:50940980 | A | AG | 16 | a0001c0001t0001g0024 a0001c0001t0001g0056 a0001c0001t0001g0184 others(13): Show |
19 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.437-2339dupG | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr13 | 50940980 | ||||||
| chr13:50941261 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.437-2060A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50941261 | |||||||
| chr13:50941303 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG01496.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.437-2018G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50941303 | |||||||
| chr13:50941359 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.437-1962T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50941359 | |||||||
| chr13:50941505 | G | C | 1 | a0001c0001t0001g0032 | 2 | NA18942.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.437-1816G>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50941505 | |||||||
| chr13:50941625 | G | A | 4 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG01891.hp1 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.437-1696G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50941625 | |||||||
| chr13:50941838 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | NA18988.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.437-1483T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50941838 | |||||||
| chr13:50941861 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.437-1460G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50941861 | |||||||
| chr13:50941936 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.437-1385G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50941936 | |||||||
| chr13:50942169 | A | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
239 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.437-1152A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50942169 | |||||||
| chr13:50942174 | A | G | 8 | a0002c0002t0002g0037 a0002c0002t0002g0041 a0002c0002t0002g0042 others(5): Show |
11 | HG02055.hp2 HG02559.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.437-1147A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50942174 | |||||||
| chr13:50942213 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.437-1108A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50942213 | |||||||
| chr13:50942302 | A | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.437-1019A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50942302 | |||||||
| chr13:50942785 | G | C | 1 | a0006c0008t0001g0091 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.437-536G>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50942785 | |||||||
| chr13:50942816 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.437-505A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50942816 | |||||||
| chr13:50942840 | G | C | 1 | a0001c0001t0001g0177 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.437-481G>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | chr13 | 50942840 | |||||||
| chr13:50943276 | AT | A | 5 | a0001c0001t0001g0184 a0001c0003t0001g0053 a0001c0003t0001g0200 others(2): Show |
6 | HG02109.hp2 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.437-35delT | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr13 | 50943276 | ||||||
| chr13:50943463 | G | A | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(68): Show |
118 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.510+69G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50943463 | |||||||
| chr13:50943610 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.510+216C>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50943610 | |||||||
| chr13:50943620 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.510+226C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50943620 | |||||||
| chr13:50944021 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.510+627G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944021 | |||||||
| chr13:50944029 | C | T | 1 | a0001c0001t0001g0046 | 2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.510+635C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944029 | |||||||
| chr13:50944045 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG01884.hp2 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.510+651G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944045 | |||||||
| chr13:50944216 | C | A | 5 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0122 others(2): Show |
7 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.510+822C>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944216 | |||||||
| chr13:50944233 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.510+839T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944233 | |||||||
| chr13:50944284 | T | G | 1 | a0001c0001t0001g0218 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.510+890T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944284 | |||||||
| chr13:50944412 | T | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0181 others(4): Show |
10 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.511-1015T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944412 | |||||||
| chr13:50944468 | A | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(134): Show |
210 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.511-959A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944468 | |||||||
| chr13:50944523 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0167 others(20): Show |
35 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.511-904G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944523 | |||||||
| chr13:50944785 | T | C | 136 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
208 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(205): Show |
intron_variant | MODIFIER | c.511-642T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944785 | |||||||
| chr13:50944878 | A | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0049 a0001c0001t0001g0181 others(4): Show |
10 | HG01891.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.511-549A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944878 | |||||||
| chr13:50944901 | A | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0183 a0001c0001t0001g0185 |
4 | HG01109.hp1 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-526A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944901 | |||||||
| chr13:50944951 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0107 a0001c0001t0001g0108 others(5): Show |
10 | HG00673.hp1 HG02027.hp2 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.511-476A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944951 | |||||||
| chr13:50944976 | A | T | 5 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0122 others(2): Show |
7 | HG02055.hp2 HG02559.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.511-451A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50944976 | |||||||
| chr13:50945036 | A | G | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(68): Show |
118 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.511-391A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 6/10 | chr13 | 50945036 | |||||||
| chr13:50945630 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.616+98G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50945630 | |||||||
| chr13:50945676 | A | G | 2 | a0001c0001t0001g0092 a0005c0007t0001g0095 |
2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.616+144A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50945676 | |||||||
| chr13:50945692 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0022 others(56): Show |
83 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(80): Show |
intron_variant | MODIFIER | c.616+160G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50945692 | |||||||
| chr13:50945730 | T | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0155 a0003c0006t0001g0139 |
3 | HG02486.hp2 HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.616+198T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50945730 | |||||||
| chr13:50945855 | G | T | 1 | a0001c0001t0001g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.616+323G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50945855 | |||||||
| chr13:50946060 | A | G | 5 | a0001c0001t0001g0184 a0001c0003t0001g0053 a0001c0003t0001g0200 others(2): Show |
6 | HG02109.hp2 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.616+528A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946060 | |||||||
| chr13:50946074 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.616+542A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946074 | |||||||
| chr13:50946138 | T | C | 15 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0046 others(12): Show |
23 | HG01074.hp1 HG01106.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.616+606T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946138 | |||||||
| chr13:50946145 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.616+613A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946145 | |||||||
| chr13:50946368 | T | G | 3 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0082 |
4 | HG02738.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.616+836T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946368 | |||||||
| chr13:50946485 | A | G | 3 | a0001c0001t0001g0050 a0001c0001t0001g0183 a0001c0001t0001g0185 |
4 | HG01109.hp1 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.616+953A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946485 | |||||||
| chr13:50946561 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.616+1029A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946561 | |||||||
| chr13:50946571 | A | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.616+1039A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946571 | |||||||
| chr13:50946633 | A | G | 1 | a0001c0001t0001g0054 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.616+1101A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946633 | |||||||
| chr13:50946888 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.617-1099G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946888 | |||||||
| chr13:50946911 | A | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | NA18997.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.617-1076A>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50946911 | |||||||
| chr13:50947027 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.617-960G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50947027 | |||||||
| chr13:50947386 | A | AGT | 13 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0145 others(10): Show |
14 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.617-564_617-563dup others(2): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947386 | A | AGTGT | 5 | a0001c0001t0001g0043 a0001c0001t0001g0133 a0001c0001t0001g0194 others(2): Show |
6 | HG02630.hp2 HG03516.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.617-566_617-563dup others(4): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947386 | A | AGTGTGT | 4 | a0001c0001t0001g0125 a0001c0001t0001g0193 a0001c0001t0001g0231 others(1): Show |
5 | HG02622.hp2 HG02970.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.617-568_617-563dup others(6): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947386 | A | AGTGTGTG others(1): Show |
18 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0016 others(15): Show |
34 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.617-570_617-563dup others(8): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947386 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0001g0196 a0002c0002t0002g0123 |
2 | NA18522.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.617-572_617-563dup others(10): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947386 | AGT | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(108): Show |
181 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.617-564_617-563del others(2): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947386 | AGTGT | A | 9 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0050 others(6): Show |
13 | HG01109.hp1 HG01256.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.617-566_617-563del others(4): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947386 | AGTGTGT | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0138 a0001c0001t0001g0156 others(2): Show |
6 | HG00438.hp1 HG02523.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.617-568_617-563del others(6): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947386 | AGTGTGTG others(1): Show |
A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0047 others(17): Show |
27 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.617-570_617-563del others(8): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947386 | AGTGTGTG others(3): Show |
A | 8 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0181 others(5): Show |
11 | HG01975.hp1 HG02109.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.617-572_617-563del others(10): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947386 | AGTGTGTG others(5): Show |
A | 1 | a0001c0001t0001g0054 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.617-574_617-563del others(12): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947386 | ||||||
| chr13:50947472 | T | C | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.617-515T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50947472 | |||||||
| chr13:50947569 | GATTT | G | 19 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0016 others(16): Show |
34 | HG00639.hp1 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.617-414_617-411del others(4): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr13 | 50947569 | ||||||
| chr13:50947663 | T | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0073 others(1): Show |
11 | HG00609.hp2 HG02027.hp1 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.617-324T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50947663 | |||||||
| chr13:50947747 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.617-240G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50947747 | |||||||
| chr13:50947814 | A | G | 1 | a0001c0001t0001g0017 | 3 | HG03017.hp2 HG03834.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.617-173A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50947814 | |||||||
| chr13:50947816 | C | T | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.617-171C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50947816 | |||||||
| chr13:50947913 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.617-74G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50947913 | |||||||
| chr13:50947976 | G | C | 1 | a0001c0001t0001g0088 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.617-11G>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 7/10 | chr13 | 50947976 | |||||||
| chr13:50948193 | A | G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.698+125A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 8/10 | chr13 | 50948193 | |||||||
| chr13:50948388 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.698+320G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 8/10 | chr13 | 50948388 | |||||||
| chr13:50948518 | AAT | A | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG02280.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.698+453_698+454del others(2): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr13 | 50948518 | ||||||
| chr13:50948672 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.698+604G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 8/10 | chr13 | 50948672 | |||||||
| chr13:50948916 | A | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0191 a0001c0001t0001g0203 |
6 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.699-547A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 8/10 | chr13 | 50948916 | |||||||
| chr13:50948930 | C | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0167 others(20): Show |
35 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.699-533C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 8/10 | chr13 | 50948930 | |||||||
| chr13:50948955 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0104 |
3 | HG01361.hp1 HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.699-508C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 8/10 | chr13 | 50948955 | |||||||
| chr13:50950063 | T | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.741+558T>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50950063 | |||||||
| chr13:50950135 | C | T | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.741+630C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50950135 | |||||||
| chr13:50950263 | T | C | 5 | a0001c0001t0001g0184 a0001c0003t0001g0053 a0001c0003t0001g0200 others(2): Show |
6 | HG02109.hp2 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+758T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50950263 | |||||||
| chr13:50950265 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.741+760T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50950265 | |||||||
| chr13:50950632 | T | C | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG01884.hp2 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.741+1127T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50950632 | |||||||
| chr13:50950644 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.741+1139G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50950644 | |||||||
| chr13:50950873 | T | C | 1 | a0001c0001t0001g0020 | 3 | HG03491.hp1 HG03492.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.741+1368T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50950873 | |||||||
| chr13:50950890 | A | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
211 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.741+1385A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50950890 | |||||||
| chr13:50951239 | C | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(127): Show |
197 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.741+1734C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50951239 | |||||||
| chr13:50951394 | G | A | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.741+1889G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50951394 | |||||||
| chr13:50951619 | T | C | 1 | a0001c0001t0001g0054 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.741+2114T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50951619 | |||||||
| chr13:50951867 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.742-2038C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50951867 | |||||||
| chr13:50951912 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.742-1993C>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50951912 | |||||||
| chr13:50952113 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.742-1792C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952113 | |||||||
| chr13:50952114 | G | T | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-1791G>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952114 | |||||||
| chr13:50952133 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.742-1772G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952133 | |||||||
| chr13:50952181 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.742-1724A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952181 | |||||||
| chr13:50952235 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.742-1670T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952235 | |||||||
| chr13:50952331 | A | G | 4 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 others(1): Show |
5 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-1574A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952331 | |||||||
| chr13:50952429 | T | C | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.742-1476T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952429 | |||||||
| chr13:50952435 | C | T | 1 | a0002c0002t0002g0105 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.742-1470C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952435 | |||||||
| chr13:50952436 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.742-1469G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952436 | |||||||
| chr13:50952557 | A | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG02572.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.742-1348A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952557 | |||||||
| chr13:50952588 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0155 a0003c0006t0001g0139 |
3 | HG02486.hp2 HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.742-1317G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952588 | |||||||
| chr13:50952622 | C | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(157): Show |
239 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.742-1283C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952622 | |||||||
| chr13:50952799 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.742-1106T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952799 | |||||||
| chr13:50952899 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.742-1006G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50952899 | |||||||
| chr13:50953019 | C | G | 8 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0143 others(5): Show |
8 | HG02071.hp1 NA18948.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.742-886C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50953019 | |||||||
| chr13:50953107 | A | G | 8 | a0002c0002t0002g0037 a0002c0002t0002g0041 a0002c0002t0002g0042 others(5): Show |
11 | HG02055.hp2 HG02559.hp1 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.742-798A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | chr13 | 50953107 | |||||||
| chr13:50953538 | CT | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0029 a0001c0001t0001g0030 others(6): Show |
18 | HG00609.hp2 HG02027.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.742-365delT | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr13 | 50953538 | ||||||
| chr13:50953991 | T | C | 4 | a0001c0001t0001g0227 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
4 | HG01891.hp1 HG02723.hp2 HG03098.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.822+6T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50953991 | |||||||
| chr13:50954029 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.822+44C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50954029 | |||||||
| chr13:50954413 | A | G | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.822+428A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50954413 | |||||||
| chr13:50954438 | G | A | 1 | a0001c0001t0001g0049 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.822+453G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50954438 | |||||||
| chr13:50954571 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.822+586G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50954571 | |||||||
| chr13:50954629 | T | G | 3 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 |
3 | HG02280.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.822+644T>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50954629 | |||||||
| chr13:50955061 | T | C | 5 | a0001c0001t0001g0184 a0001c0003t0001g0053 a0001c0003t0001g0200 others(2): Show |
6 | HG02109.hp2 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.822+1076T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50955061 | |||||||
| chr13:50955103 | A | AACAGTGT others(54): Show |
1 | a0001c0001t0001g0193 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.822+1119_822+1179d others(63): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr13 | 50955103 | ||||||
| chr13:50955105 | C | G | 23 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0167 others(20): Show |
35 | HG00597.hp1 HG00741.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.822+1120C>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50955105 | |||||||
| chr13:50955240 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.823-1118C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50955240 | |||||||
| chr13:50955323 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.823-1035G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50955323 | |||||||
| chr13:50955335 | GCCCAA | G | 3 | a0001c0004t0001g0045 a0001c0004t0001g0164 a0001c0004t0001g0165 |
4 | HG02145.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-1022_823-1018d others(7): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50955335 | |||||||
| chr13:50955581 | T | C | 5 | a0001c0001t0001g0184 a0001c0003t0001g0053 a0001c0003t0001g0200 others(2): Show |
6 | HG02109.hp2 HG02145.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-777T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50955581 | |||||||
| chr13:50955588 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.823-770C>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50955588 | |||||||
| chr13:50955608 | A | G | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.823-750A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50955608 | |||||||
| chr13:50955657 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(128): Show |
202 | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(199): Show |
intron_variant | MODIFIER | c.823-701C>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50955657 | |||||||
| chr13:50955791 | T | TAGAAATG others(150): Show |
1 | a0001c0001t0001g0193 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.823-557_823-556ins others(157): Show |
RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr13 | 50955791 | ||||||
| chr13:50956056 | T | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0223 |
2 | NA18982.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.823-302T>C | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50956056 | |||||||
| chr13:50956094 | C | A | 1 | a0001c0001t0001g0043 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.823-264C>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50956094 | |||||||
| chr13:50956278 | A | T | 22 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0049 others(19): Show |
28 | HG00099.hp1 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.823-80A>T | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50956278 | |||||||
| chr13:50956283 | G | A | 6 | a0001c0001t0001g0018 a0001c0001t0001g0108 a0001c0001t0001g0109 others(3): Show |
8 | HG00673.hp1 NA18961.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.823-75G>A | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50956283 | |||||||
| chr13:50956325 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.823-33A>G | RNASEH2B | ENSG00000136104.21 | transcript | ENST00000336617.8 | protein_coding | 10/10 | chr13 | 50956325 |