Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83852 |
| ensemblid | ENSG00000136169.17 |
| hgncid | 20263 |
| symbol | SETDB2 |
| name | SET domain bifurcated histone lysine methyltransferase 2 |
| refseq_nuc | NM_001160308.3 |
| refseq_prot | NP_001153780.1 |
| ensembl_nuc | ENST00000611815.2 |
| ensembl_prot | ENSP00000482240.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 49444274 |
| end | 49495003 |
| strand | + |
| ver | v1.2 |
| region | chr13:49444274-49495003 |
| region5000 | chr13:49439274-49500003 |
| regionname0 | SETDB2_chr13_49444274_49495003 |
| regionname5000 | SETDB2_chr13_49439274_49500003 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 707 | 289 | 54 | 48 | 161 | 8 | 17 | 127 | SETDB2_chr13_49439274_49500003 | SETDB2 | MGEKN others(702): Show |
chr13 | 49439274 | 49500003 |
| a0002 | 1/0 | 707 | 59 | 4 | 19 | 22 | 4 | 9 | 17 | SETDB2_chr13_49439274_49500003 | SETDB2 | MGEKN others(702): Show |
chr13 | 49439274 | 49500003 |
| a0003 | 0/0 | 707 | 34 | 16 | 3 | 9 | 0 | 6 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | MGEKN others(702): Show |
chr13 | 49439274 | 49500003 |
| a0004 | 0/0 | 707 | 14 | 13 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | MGEKN others(702): Show |
chr13 | 49439274 | 49500003 |
| a0005 | 0/0 | 707 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | MGEKN others(702): Show |
chr13 | 49439274 | 49500003 |
| a0006 | 0/0 | 707 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | MGEKN others(702): Show |
chr13 | 49439274 | 49500003 |
| a0007 | 0/0 | 707 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | MGEKN others(702): Show |
chr13 | 49439274 | 49500003 |
| a0008 | 0/0 | 666 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | MGEKN others(661): Show |
chr13 | 49439274 | 49500003 |
| a0009 | 0/0 | 707 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | MGEKN others(702): Show |
chr13 | 49439274 | 49500003 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2121 | 169 | 35 | 29 | 87 | 7 | 10 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0001c0002 | 0/0 | 2121 | 115 | 17 | 19 | 72 | 1 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0001c0008 | 0/0 | 2121 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0001c0010 | 0/0 | 2121 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0001c0012 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0001c0014 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0002c0003 | 1/0 | 2121 | 59 | 4 | 19 | 22 | 4 | 9 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0003c0004 | 0/0 | 2121 | 34 | 16 | 3 | 9 | 0 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0004c0005 | 0/0 | 2121 | 14 | 13 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0005c0006 | 0/0 | 2121 | 5 | 0 | 5 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0006c0007 | 0/0 | 2121 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0007c0009 | 0/0 | 2121 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 | ||
| a0008c0011 | 0/0 | 2108 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2103): Show |
chr13 | 49439274 | 49500003 | ||
| a0009c0013 | 0/0 | 2121 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | ATGGG others(2116): Show |
chr13 | 49439274 | 49500003 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6200 | 127 | 8 | 25 | 77 | 7 | 10 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6195): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0005 | 0/0 | 6203 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0007 | 0/0 | 6201 | 11 | 9 | 1 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0010 | 0/0 | 6201 | 6 | 5 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0013 | 0/0 | 6202 | 4 | 3 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0016 | 0/0 | 6200 | 4 | 0 | 0 | 4 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6195): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0017 | 0/0 | 6201 | 3 | 2 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0021 | 0/0 | 6202 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0023 | 0/0 | 6200 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6195): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0027 | 0/0 | 6201 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0028 | 0/0 | 6201 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0037 | 0/0 | 6202 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0040 | 0/1 | 6196 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6191): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0041 | 0/0 | 6200 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6195): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0042 | 0/0 | 6200 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6195): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0043 | 0/0 | 6200 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6195): Show |
chr13 | 49439274 | 49500003 |
| a0001c0001t0045 | 0/0 | 6201 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0003 | 0/0 | 6202 | 38 | 1 | 8 | 28 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0004 | 0/0 | 6201 | 36 | 4 | 1 | 26 | 1 | 4 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0007 | 0/0 | 6201 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0008 | 0/0 | 6202 | 6 | 1 | 5 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0009 | 0/0 | 6201 | 10 | 0 | 0 | 10 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0011 | 0/0 | 6202 | 3 | 0 | 3 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0012 | 0/0 | 6204 | 5 | 5 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6199): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0014 | 0/0 | 6202 | 4 | 0 | 0 | 4 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0019 | 0/0 | 6201 | 3 | 3 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0022 | 0/0 | 6201 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0024 | 0/0 | 6201 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0025 | 0/0 | 6201 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0026 | 0/0 | 6201 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0029 | 0/0 | 6201 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0030 | 0/0 | 6201 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0001c0002t0036 | 0/0 | 6202 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0001c0008t0005 | 0/0 | 6203 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0001c0010t0001 | 0/0 | 6200 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6195): Show |
chr13 | 49439274 | 49500003 |
| a0001c0012t0038 | 0/0 | 6200 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6195): Show |
chr13 | 49439274 | 49500003 |
| a0001c0014t0003 | 0/0 | 6202 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0002c0003t0002 | 1/0 | 6203 | 45 | 3 | 15 | 17 | 1 | 8 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0002c0003t0008 | 0/0 | 6202 | 6 | 0 | 3 | 0 | 3 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0002c0003t0015 | 0/0 | 6201 | 4 | 0 | 0 | 4 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0002c0003t0033 | 0/0 | 6203 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0002c0003t0034 | 0/0 | 6203 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0002c0003t0035 | 0/0 | 6203 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0002c0003t0044 | 0/0 | 6200 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6195): Show |
chr13 | 49439274 | 49500003 |
| a0003c0004t0005 | 0/0 | 6203 | 28 | 11 | 2 | 9 | 0 | 6 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0003c0004t0018 | 0/0 | 6203 | 3 | 2 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0003c0004t0020 | 0/0 | 6203 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0003c0004t0031 | 0/0 | 6203 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0003c0004t0032 | 0/0 | 6203 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0004c0005t0006 | 0/0 | 6201 | 14 | 13 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| a0005c0006t0003 | 0/0 | 6202 | 5 | 0 | 5 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0006c0007t0011 | 0/0 | 6202 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6197): Show |
chr13 | 49439274 | 49500003 |
| a0007c0009t0020 | 0/0 | 6203 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6198): Show |
chr13 | 49439274 | 49500003 |
| a0008c0011t0039 | 0/0 | 6198 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6193): Show |
chr13 | 49439274 | 49500003 |
| a0009c0013t0004 | 0/0 | 6201 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | GGAGG others(6196): Show |
chr13 | 49439274 | 49500003 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0007g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0007g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0007g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0007g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0010g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0010g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0010g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0010g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0013g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0013g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0013g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0016g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0016g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0016g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0017g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0017g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0017g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0021g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0021g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0023g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0023g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0027g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0028g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0037g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0040g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0041g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0042g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0043g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0001t0045g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0004g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0007g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0008g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0008g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0008g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0008g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0008g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0009g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0009g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0009g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0009g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0009g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0009g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0009g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0009g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0009g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0011g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0011g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0011g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0012g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0012g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0012g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0014g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0014g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0014g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0014g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0019g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0019g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0019g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0022g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0022g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0024g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0025g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0026g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0029g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0030g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0002t0036g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0008t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0010t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0012t0038g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0001c0014t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0310 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0008g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0008g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0008g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0008g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0008g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0015g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0015g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0015g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0015g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0033g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0034g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0035g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0002c0003t0044g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0005g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0018g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0018g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0018g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0020g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0031g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0003c0004t0032g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0004c0005t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0005c0006t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0005c0006t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0005c0006t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0006c0007t0011g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0006c0007t0011g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0007c0009t0020g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0008c0011t0039g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| a0009c0013t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00140 | hp2 | a0002 | c0003 | t0002 | g0285 | EUR | GBR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00280 | hp1 | a0002 | c0003 | t0008 | g0288 | EUR | FIN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | FIN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0246 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00408 | hp2 | a0001 | c0002 | t0004 | g0372 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00438 | hp1 | a0001 | c0001 | t0042 | g0144 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00558 | hp2 | a0001 | c0002 | t0009 | g0373 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00597 | hp1 | a0001 | c0014 | t0003 | g0264 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00609 | hp2 | a0002 | c0003 | t0015 | g0317 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00639 | hp1 | a0001 | c0002 | t0008 | g0269 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00642 | hp1 | a0001 | c0002 | t0004 | g0369 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00642 | hp2 | a0005 | c0006 | t0003 | g0013 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00733 | hp2 | a0002 | c0003 | t0002 | g0018 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00735 | hp1 | a0002 | c0003 | t0002 | g0314 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00738 | hp1 | a0006 | c0007 | t0011 | g0244 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00738 | hp2 | a0002 | c0003 | t0002 | g0301 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00741 | hp1 | a0001 | c0002 | t0008 | g0273 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01069 | hp1 | a0002 | c0003 | t0008 | g0017 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01070 | hp1 | a0002 | c0003 | t0002 | g0020 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01071 | hp2 | a0002 | c0003 | t0002 | g0019 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01074 | hp1 | a0001 | c0001 | t0013 | g0061 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01074 | hp2 | a0001 | c0002 | t0011 | g0268 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01081 | hp1 | a0001 | c0002 | t0011 | g0272 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01081 | hp2 | a0005 | c0006 | t0003 | g0236 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01099 | hp2 | a0002 | c0003 | t0002 | g0300 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01106 | hp1 | a0001 | c0001 | t0007 | g0064 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01106 | hp2 | a0002 | c0003 | t0002 | g0313 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01109 | hp1 | a0003 | c0004 | t0018 | g0197 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01109 | hp2 | a0003 | c0004 | t0005 | g0202 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01168 | hp2 | a0006 | c0007 | t0011 | g0245 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0230 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01243 | hp1 | a0004 | c0005 | t0006 | g0068 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01243 | hp2 | a0001 | c0001 | t0017 | g0030 | AMR | PUR | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01255 | hp2 | a0005 | c0006 | t0003 | g0014 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01257 | hp1 | a0001 | c0002 | t0007 | g0011 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01257 | hp2 | a0003 | c0004 | t0005 | g0203 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01258 | hp1 | a0001 | c0002 | t0011 | g0271 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01258 | hp2 | a0001 | c0002 | t0007 | g0011 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01261 | hp1 | a0002 | c0003 | t0008 | g0289 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01261 | hp2 | a0001 | c0002 | t0008 | g0270 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01358 | hp2 | a0001 | c0002 | t0008 | g0276 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0235 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | IBS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01517 | hp2 | a0002 | c0003 | t0008 | g0017 | EUR | IBS | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01884 | hp1 | a0004 | c0005 | t0006 | g0069 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0190 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01928 | hp2 | a0002 | c0003 | t0002 | g0298 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01934 | hp1 | a0002 | c0003 | t0002 | g0302 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01943 | hp2 | a0002 | c0003 | t0002 | g0294 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01952 | hp1 | a0001 | c0002 | t0003 | g0237 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01952 | hp2 | a0002 | c0003 | t0002 | g0296 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01975 | hp1 | a0002 | c0003 | t0033 | g0023 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01975 | hp2 | a0001 | c0001 | t0010 | g0160 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01978 | hp1 | a0002 | c0003 | t0002 | g0293 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0239 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0279 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01993 | hp1 | a0002 | c0003 | t0002 | g0295 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01993 | hp2 | a0001 | c0002 | t0008 | g0274 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0277 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02015 | hp1 | a0003 | c0004 | t0005 | g0231 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02015 | hp2 | a0001 | c0002 | t0004 | g0375 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02027 | hp1 | a0001 | c0002 | t0004 | g0330 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02040 | hp2 | a0002 | c0003 | t0002 | g0328 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0159 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02056 | hp1 | a0002 | c0003 | t0002 | g0323 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02056 | hp2 | a0001 | c0002 | t0004 | g0355 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02071 | hp2 | a0001 | c0002 | t0014 | g0262 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02074 | hp1 | a0001 | c0002 | t0003 | g0258 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02080 | hp1 | a0001 | c0002 | t0014 | g0263 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0260 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02083 | hp1 | a0002 | c0003 | t0044 | g0304 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02083 | hp2 | a0003 | c0004 | t0005 | g0216 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02132 | hp1 | a0001 | c0002 | t0025 | g0022 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02132 | hp2 | a0003 | c0004 | t0005 | g0206 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02135 | hp1 | a0001 | c0002 | t0004 | g0353 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02145 | hp1 | a0004 | c0005 | t0006 | g0067 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02145 | hp2 | a0003 | c0004 | t0005 | g0223 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02148 | hp1 | a0002 | c0003 | t0002 | g0299 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0238 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02155 | hp1 | a0001 | c0002 | t0004 | g0344 | EAS | CDX | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0259 | EAS | CDX | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02165 | hp1 | a0002 | c0003 | t0015 | g0320 | EAS | CDX | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02257 | hp1 | a0001 | c0001 | t0027 | g0189 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02257 | hp2 | a0004 | c0005 | t0006 | g0076 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02258 | hp1 | a0004 | c0005 | t0006 | g0066 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02258 | hp2 | a0001 | c0001 | t0045 | g0161 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02273 | hp1 | a0001 | c0002 | t0003 | g0278 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02273 | hp2 | a0002 | c0003 | t0002 | g0297 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02280 | hp1 | a0002 | c0003 | t0034 | g0306 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0171 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02293 | hp1 | a0005 | c0006 | t0003 | g0013 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02300 | hp1 | a0005 | c0006 | t0003 | g0014 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02451 | hp1 | a0004 | c0005 | t0006 | g0072 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02451 | hp2 | a0003 | c0004 | t0005 | g0210 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02523 | hp1 | a0001 | c0002 | t0003 | g0261 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02572 | hp1 | a0003 | c0004 | t0005 | g0213 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02572 | hp2 | a0001 | c0002 | t0019 | g0275 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02602 | hp1 | a0001 | c0002 | t0024 | g0371 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02602 | hp2 | a0003 | c0004 | t0005 | g0201 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02622 | hp1 | a0003 | c0004 | t0005 | g0205 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02622 | hp2 | a0004 | c0005 | t0006 | g0077 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0082 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0170 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02647 | hp1 | a0003 | c0004 | t0020 | g0194 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02647 | hp2 | a0001 | c0001 | t0010 | g0054 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02698 | hp1 | a0001 | c0002 | t0004 | g0361 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02698 | hp2 | a0003 | c0004 | t0005 | g0006 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02717 | hp1 | a0001 | c0008 | t0005 | g0009 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02717 | hp2 | a0001 | c0001 | t0010 | g0193 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02723 | hp2 | a0001 | c0001 | t0013 | g0063 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02738 | hp2 | a0002 | c0003 | t0002 | g0305 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02818 | hp1 | a0001 | c0002 | t0012 | g0281 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02818 | hp2 | a0004 | c0005 | t0006 | g0070 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02886 | hp1 | a0003 | c0004 | t0005 | g0207 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02886 | hp2 | a0001 | c0002 | t0026 | g0329 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0015 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02895 | hp2 | a0003 | c0004 | t0018 | g0196 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02896 | hp1 | a0001 | c0002 | t0019 | g0267 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02896 | hp2 | a0004 | c0005 | t0006 | g0075 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0015 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02897 | hp2 | a0004 | c0005 | t0006 | g0065 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02922 | hp1 | a0001 | c0001 | t0017 | g0029 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02922 | hp2 | a0001 | c0002 | t0012 | g0280 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02970 | hp1 | a0003 | c0004 | t0031 | g0199 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02976 | hp1 | a0007 | c0009 | t0020 | g0195 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02976 | hp2 | a0003 | c0004 | t0005 | g0209 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03017 | hp1 | a0001 | c0002 | t0004 | g0370 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03017 | hp2 | a0002 | c0003 | t0035 | g0291 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03041 | hp1 | a0001 | c0001 | t0021 | g0059 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03041 | hp2 | a0003 | c0004 | t0005 | g0208 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03098 | hp1 | a0004 | c0005 | t0006 | g0073 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03130 | hp2 | a0001 | c0002 | t0004 | g0265 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0079 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03139 | hp2 | a0001 | c0008 | t0005 | g0009 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0081 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0333 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0080 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03209 | hp2 | a0002 | c0003 | t0002 | g0084 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03225 | hp2 | a0001 | c0001 | t0021 | g0062 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03239 | hp1 | a0002 | c0003 | t0002 | g0018 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03453 | hp1 | a0001 | c0001 | t0017 | g0028 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03453 | hp2 | a0001 | c0002 | t0012 | g0016 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03486 | hp1 | a0001 | c0001 | t0013 | g0060 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0003 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03490 | hp1 | a0003 | c0004 | t0005 | g0006 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03492 | hp1 | a0003 | c0004 | t0005 | g0006 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03492 | hp2 | a0002 | c0003 | t0002 | g0309 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03516 | hp1 | a0003 | c0004 | t0005 | g0211 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03540 | hp2 | a0001 | c0001 | t0041 | g0117 | AFR | GWD | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03579 | hp1 | a0001 | c0002 | t0029 | g0228 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03579 | hp2 | a0002 | c0003 | t0002 | g0085 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03688 | hp2 | a0001 | c0002 | t0004 | g0356 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03704 | hp2 | a0001 | c0010 | t0001 | g0108 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03710 | hp2 | a0002 | c0003 | t0002 | g0311 | SAS | PJL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03834 | hp1 | a0002 | c0003 | t0002 | g0324 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03927 | hp2 | a0002 | c0003 | t0002 | g0312 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03942 | hp1 | a0002 | c0003 | t0002 | g0303 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03942 | hp2 | a0003 | c0004 | t0005 | g0212 | SAS | BEB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG04199 | hp2 | a0003 | c0004 | t0005 | g0200 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG04204 | hp1 | a0001 | c0002 | t0004 | g0357 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18522 | hp1 | a0001 | c0002 | t0012 | g0282 | AFR | YRI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18522 | hp2 | a0001 | c0002 | t0004 | g0266 | AFR | YRI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18612 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | CHB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18612 | hp2 | a0001 | c0001 | t0043 | g0138 | EAS | CHB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18747 | hp2 | a0001 | c0002 | t0014 | g0242 | EAS | CHB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18939 | hp2 | a0001 | c0002 | t0004 | g0220 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18940 | hp1 | a0001 | c0002 | t0004 | g0359 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18940 | hp2 | a0008 | c0011 | t0039 | g0050 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18942 | hp1 | a0001 | c0002 | t0004 | g0351 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18943 | hp1 | a0001 | c0002 | t0004 | g0350 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18943 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18945 | hp2 | a0001 | c0002 | t0004 | g0337 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0250 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18947 | hp1 | a0003 | c0004 | t0005 | g0214 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18947 | hp2 | a0002 | c0003 | t0002 | g0283 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18948 | hp1 | a0001 | c0002 | t0004 | g0338 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18950 | hp1 | a0002 | c0003 | t0002 | g0308 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18952 | hp1 | a0001 | c0002 | t0022 | g0339 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18953 | hp1 | a0003 | c0004 | t0005 | g0374 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18954 | hp1 | a0001 | c0001 | t0007 | g0164 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18959 | hp2 | a0001 | c0002 | t0004 | g0334 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18960 | hp1 | a0003 | c0004 | t0005 | g0217 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18961 | hp2 | a0002 | c0003 | t0002 | g0325 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18962 | hp2 | a0003 | c0004 | t0005 | g0215 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18964 | hp2 | a0002 | c0003 | t0015 | g0321 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18966 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0252 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18969 | hp1 | a0001 | c0002 | t0014 | g0249 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18969 | hp2 | a0001 | c0001 | t0023 | g0120 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0233 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18972 | hp1 | a0001 | c0002 | t0003 | g0241 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0253 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18973 | hp2 | a0001 | c0002 | t0009 | g0366 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18974 | hp1 | a0001 | c0002 | t0022 | g0336 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18977 | hp1 | a0001 | c0002 | t0004 | g0349 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18977 | hp2 | a0001 | c0002 | t0003 | g0240 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0232 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18980 | hp2 | a0002 | c0003 | t0015 | g0322 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0248 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18983 | hp1 | a0001 | c0002 | t0009 | g0367 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18984 | hp2 | a0002 | c0003 | t0002 | g0319 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18985 | hp2 | a0001 | c0002 | t0004 | g0346 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18986 | hp1 | a0002 | c0003 | t0002 | g0318 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18987 | hp2 | a0001 | c0002 | t0003 | g0226 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18988 | hp1 | a0001 | c0002 | t0009 | g0363 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18989 | hp2 | a0001 | c0002 | t0004 | g0354 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18994 | hp2 | a0002 | c0003 | t0002 | g0327 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18998 | hp1 | a0001 | c0002 | t0009 | g0022 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18998 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19001 | hp2 | a0003 | c0004 | t0005 | g0219 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19003 | hp2 | a0001 | c0002 | t0009 | g0362 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19004 | hp1 | a0002 | c0003 | t0002 | g0284 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19004 | hp2 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19005 | hp1 | a0001 | c0012 | t0038 | g0143 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19006 | hp1 | a0002 | c0003 | t0002 | g0315 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19006 | hp2 | a0001 | c0002 | t0003 | g0286 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19007 | hp1 | a0001 | c0002 | t0009 | g0364 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19007 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19009 | hp1 | a0001 | c0001 | t0023 | g0133 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19009 | hp2 | a0001 | c0002 | t0004 | g0345 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19010 | hp2 | a0002 | c0003 | t0002 | g0020 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19011 | hp2 | a0001 | c0001 | t0016 | g0002 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19030 | hp1 | a0001 | c0001 | t0028 | g0191 | AFR | LWK | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19030 | hp2 | a0003 | c0004 | t0005 | g0204 | AFR | LWK | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19055 | hp1 | a0001 | c0002 | t0003 | g0247 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19055 | hp2 | a0002 | c0003 | t0002 | g0326 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19057 | hp1 | a0001 | c0001 | t0016 | g0039 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19057 | hp2 | a0001 | c0002 | t0004 | g0360 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19060 | hp1 | a0001 | c0002 | t0004 | g0340 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19062 | hp1 | a0001 | c0002 | t0004 | g0342 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19064 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19064 | hp2 | a0001 | c0002 | t0009 | g0021 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19066 | hp2 | a0001 | c0002 | t0004 | g0335 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19068 | hp1 | a0001 | c0002 | t0004 | g0347 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19068 | hp2 | a0001 | c0002 | t0003 | g0254 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19072 | hp1 | a0001 | c0002 | t0036 | g0234 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19072 | hp2 | a0001 | c0002 | t0004 | g0348 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19076 | hp1 | a0001 | c0002 | t0004 | g0341 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19077 | hp1 | a0001 | c0002 | t0003 | g0257 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19078 | hp1 | a0001 | c0002 | t0004 | g0343 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19078 | hp2 | a0001 | c0001 | t0037 | g0102 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19080 | hp1 | a0001 | c0002 | t0003 | g0251 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19081 | hp2 | a0001 | c0002 | t0004 | g0358 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19084 | hp1 | a0001 | c0002 | t0003 | g0225 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19085 | hp2 | a0002 | c0003 | t0002 | g0007 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19086 | hp2 | a0002 | c0003 | t0002 | g0316 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19087 | hp2 | a0003 | c0004 | t0005 | g0218 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19088 | hp2 | a0001 | c0002 | t0009 | g0021 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19089 | hp1 | a0001 | c0001 | t0016 | g0038 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19089 | hp2 | a0002 | c0003 | t0002 | g0307 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0256 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19090 | hp2 | a0001 | c0002 | t0009 | g0365 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19240 | hp1 | a0003 | c0004 | t0005 | g0224 | AFR | YRI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA19240 | hp2 | a0004 | c0005 | t0006 | g0074 | AFR | YRI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0255 | AFR | ASW | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA20129 | hp2 | a0003 | c0004 | t0018 | g0198 | AFR | ASW | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA20752 | hp1 | a0001 | c0002 | t0004 | g0331 | EUR | TSI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | TSI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA20805 | hp2 | a0002 | c0003 | t0008 | g0287 | EUR | TSI | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA20905 | hp1 | a0002 | c0003 | t0002 | g0292 | SAS | GIH | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA20905 | hp2 | a0001 | c0002 | t0003 | g0229 | SAS | GIH | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01123 | hp1 | a0002 | c0003 | t0008 | g0290 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02109 | hp1 | a0004 | c0005 | t0006 | g0024 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02109 | hp2 | a0003 | c0004 | t0032 | g0222 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0003 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02559 | hp1 | a0001 | c0002 | t0008 | g0243 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0083 | AFR | ACB | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03471 | hp1 | a0001 | c0002 | t0012 | g0016 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG03471 | hp2 | a0001 | c0002 | t0019 | g0227 | AFR | MSL | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | USA | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| HG06807 | hp2 | a0002 | c0003 | t0002 | g0019 | AFR | USA | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA18955 | hp2 | a0009 | c0013 | t0004 | g0352 | EAS | JPT | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0332 | AFR | USA | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA20300 | hp2 | a0004 | c0005 | t0006 | g0071 | AFR | USA | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA21309 | hp1 | a0001 | c0002 | t0030 | g0368 | AFR | LWK | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| NA21309 | hp2 | a0003 | c0004 | t0005 | g0221 | AFR | LWK | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0040 | g0155 | REF | REF | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0002 | g0310 | REF | REF | SETDB2_chr13_49439274_49500003 | SETDB2 | chr13 | 49439274 | 49500003 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49476484 | A | G | 6 | a0001 a0004 a0005 others(3): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
missense_variant | MODERATE | c.314A>G | p.Glu105Gly | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/14 | 1239/6203 | 314/2124 | 105/707 | chr13 | 49476484 | |||
| chr13:49476973 | A | G | 1 | a0009 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.803A>G | p.Tyr268Cys | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/14 | 1728/6203 | 803/2124 | 268/707 | chr13 | 49476973 | |||
| chr13:49482767 | A | T | 1 | a0004 | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
missense_variant | MODERATE | c.1187A>T | p.Lys396Ile | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2112/6203 | 1187/2124 | 396/707 | chr13 | 49482767 | |||
| chr13:49482790 | G | A | 1 | a0005 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.1210G>A | p.Gly404Arg | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2135/6203 | 1210/2124 | 404/707 | chr13 | 49482790 | |||
| chr13:49482860 | G | C | 1 | a0007 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1280G>C | p.Cys427Ser | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2205/6203 | 1280/2124 | 427/707 | chr13 | 49482860 | |||
| chr13:49482907 | G | A | 1 | a0006 | 2 | HG00738.hp1 HG01168.hp2 |
missense_variant | MODERATE | c.1327G>A | p.Ala443Thr | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2252/6203 | 1327/2124 | 443/707 | chr13 | 49482907 | |||
| chr13:49482961 | G | A | 8 | a0001 a0003 a0004 others(5): Show |
346 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(343): Show |
missense_variant&splice_region_variant | MODERATE | c.1381G>A | p.Val461Met | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2306/6203 | 1381/2124 | 461/707 | chr13 | 49482961 | |||
| chr13:49490897 | TTCTTCAC others(13): Show |
T | 1 | a0008 | 1 | NA18940.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1994_2006+7delTCTT others(16): Show |
p.Phe665fs | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/14 | 2919/6203 | 1994/2124 | 665/707 | chr13 | 49490897 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49467916 | C | T | 1 | a0001c0008 | 2 | HG02717.hp1 HG03139.hp2 |
synonymous_variant | LOW | c.261C>T | p.Pro87Pro | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/14 | 1186/6203 | 261/2124 | 87/707 | chr13 | 49467916 | |||
| chr13:49476650 | C | T | 1 | a0001c0014 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.480C>T | p.His160His | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/14 | 1405/6203 | 480/2124 | 160/707 | chr13 | 49476650 | |||
| chr13:49482768 | A | G | 1 | a0001c0012 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.1188A>G | p.Lys396Lys | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2113/6203 | 1188/2124 | 396/707 | chr13 | 49482768 | |||
| chr13:49482780 | T | C | 1 | a0001c0010 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1200T>C | p.Ile400Ile | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/14 | 2125/6203 | 1200/2124 | 400/707 | chr13 | 49482780 | |||
| chr13:49483497 | A | G | 5 | a0001c0001 a0001c0008 a0001c0010 others(2): Show |
173 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(170): Show |
synonymous_variant | LOW | c.1416A>G | p.Gln472Gln | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/14 | 2341/6203 | 1416/2124 | 472/707 | chr13 | 49483497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49444373 | AC | A | 1 | a0001c0002t0019 | 3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-824delC | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7519 | INFO_REALIGN_3_PRIME | chr13 | 49444373 | |||||
| chr13:49444482 | G | A | 1 | a0001c0002t0024 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-717G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7412 | chr13 | 49444482 | ||||||
| chr13:49444505 | C | T | 1 | a0001c0002t0012 | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-694C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7389 | chr13 | 49444505 | ||||||
| chr13:49444554 | G | C | 2 | a0003c0004t0020 a0007c0009t0020 |
2 | HG02647.hp1 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-645G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7340 | chr13 | 49444554 | ||||||
| chr13:49444602 | G | C | 1 | a0001c0002t0012 | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-597G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7292 | chr13 | 49444602 | ||||||
| chr13:49444641 | C | T | 2 | a0001c0001t0010 a0001c0001t0045 |
7 | HG01975.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-558C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7253 | chr13 | 49444641 | ||||||
| chr13:49444686 | C | T | 2 | a0001c0002t0011 a0006c0007t0011 |
5 | HG00738.hp1 HG01074.hp2 HG01081.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-513C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7208 | chr13 | 49444686 | ||||||
| chr13:49444692 | G | A | 1 | a0001c0002t0025 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-507G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7202 | chr13 | 49444692 | ||||||
| chr13:49444704 | CA | C | 11 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0023 others(8): Show |
141 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
5_prime_UTR_variant | MODIFIER | c.-494delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7189 | chr13 | 49444704 | ||||||
| chr13:49444705 | A | G | 8 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0013 others(5): Show |
28 | HG01074.hp1 HG01106.hp1 HG01243.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-494A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7189 | chr13 | 49444705 | ||||||
| chr13:49444706 | T | G | 11 | a0001c0001t0001 a0001c0001t0016 a0001c0001t0023 others(8): Show |
141 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(138): Show |
5_prime_UTR_variant | MODIFIER | c.-493T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7188 | chr13 | 49444706 | ||||||
| chr13:49444740 | G | A | 1 | a0001c0002t0012 | 5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-459G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/14 | 7154 | chr13 | 49444740 | ||||||
| chr13:49451874 | T | G | 1 | a0001c0002t0026 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/14 | 20 | chr13 | 49451874 | ||||||
| chr13:49491917 | T | A | 1 | a0001c0001t0016 | 4 | NA19004.hp2 NA19011.hp2 NA19057.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*68T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 68 | chr13 | 49491917 | ||||||
| chr13:49492222 | C | A | 1 | a0001c0001t0027 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 373 | chr13 | 49492222 | ||||||
| chr13:49492252 | A | G | 1 | a0004c0005t0006 | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*403A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 403 | chr13 | 49492252 | ||||||
| chr13:49492353 | A | G | 1 | a0001c0001t0023 | 2 | NA18969.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*504A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 504 | chr13 | 49492353 | ||||||
| chr13:49492388 | G | A | 19 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(16): Show |
171 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*539G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 539 | chr13 | 49492388 | ||||||
| chr13:49492495 | C | T | 1 | a0001c0002t0036 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*646C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 646 | chr13 | 49492495 | ||||||
| chr13:49492507 | T | A | 48 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(45): Show |
352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*658T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 658 | chr13 | 49492507 | ||||||
| chr13:49492527 | G | A | 1 | a0001c0002t0009 | 10 | HG00558.hp2 NA18973.hp2 NA18983.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*678G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 678 | chr13 | 49492527 | ||||||
| chr13:49492585 | C | T | 48 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(45): Show |
352 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*736C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 736 | chr13 | 49492585 | ||||||
| chr13:49492842 | T | C | 39 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(36): Show |
308 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*993T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 993 | chr13 | 49492842 | ||||||
| chr13:49492948 | ACT | A | 2 | a0002c0003t0015 a0002c0003t0044 |
5 | HG00609.hp2 HG02083.hp1 HG02165.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1107_*1108delTC | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1107 | INFO_REALIGN_3_PRIME | chr13 | 49492948 | |||||
| chr13:49492962 | A | G | 5 | a0001c0002t0003 a0001c0002t0014 a0001c0002t0036 others(2): Show |
49 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1113A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1113 | chr13 | 49492962 | ||||||
| chr13:49492968 | GCA | G | 38 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(35): Show |
307 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(304): Show |
3_prime_UTR_variant | MODIFIER | c.*1135_*1136delAC | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1135 | INFO_REALIGN_3_PRIME | chr13 | 49492968 | |||||
| chr13:49493049 | A | C | 5 | a0001c0001t0005 a0001c0002t0012 a0001c0008t0005 others(2): Show |
38 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1200A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1200 | chr13 | 49493049 | ||||||
| chr13:49493052 | C | CT | 13 | a0001c0001t0013 a0001c0001t0021 a0001c0002t0003 others(10): Show |
80 | HG00280.hp1 HG00408.hp1 HG00597.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1213dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1214 | INFO_REALIGN_3_PRIME | chr13 | 49493052 | |||||
| chr13:49493110 | G | C | 39 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(36): Show |
308 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*1261G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1261 | chr13 | 49493110 | ||||||
| chr13:49493121 | T | C | 1 | a0001c0002t0014 | 4 | HG02071.hp2 HG02080.hp1 NA18747.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1272T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1272 | chr13 | 49493121 | ||||||
| chr13:49493152 | C | T | 1 | a0001c0001t0042 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1303C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1303 | chr13 | 49493152 | ||||||
| chr13:49493250 | G | A | 1 | a0004c0005t0006 | 14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1401G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1401 | chr13 | 49493250 | ||||||
| chr13:49493306 | T | C | 39 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(36): Show |
308 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(305): Show |
3_prime_UTR_variant | MODIFIER | c.*1457T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1457 | chr13 | 49493306 | ||||||
| chr13:49493307 | G | A | 19 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(16): Show |
172 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*1458G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1458 | chr13 | 49493307 | ||||||
| chr13:49493329 | G | A | 1 | a0001c0012t0038 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1480G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1480 | chr13 | 49493329 | ||||||
| chr13:49493357 | T | C | 1 | a0002c0003t0033 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1508T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1508 | chr13 | 49493357 | ||||||
| chr13:49493636 | T | C | 1 | a0002c0003t0034 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1787T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1787 | chr13 | 49493636 | ||||||
| chr13:49493737 | G | C | 3 | a0003c0004t0018 a0003c0004t0020 a0007c0009t0020 |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1888G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1888 | chr13 | 49493737 | ||||||
| chr13:49493788 | T | C | 3 | a0003c0004t0018 a0003c0004t0020 a0007c0009t0020 |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1939T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1939 | chr13 | 49493788 | ||||||
| chr13:49493829 | C | A | 1 | a0001c0001t0045 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1980C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1980 | chr13 | 49493829 | ||||||
| chr13:49493848 | T | C | 1 | a0003c0004t0031 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1999T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 1999 | chr13 | 49493848 | ||||||
| chr13:49494168 | C | T | 2 | a0001c0001t0027 a0001c0001t0028 |
2 | HG02257.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2319C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2319 | chr13 | 49494168 | ||||||
| chr13:49494169 | A | G | 1 | a0001c0001t0041 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2320A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2320 | chr13 | 49494169 | ||||||
| chr13:49494211 | G | A | 1 | a0001c0001t0021 | 2 | HG03041.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2362G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2362 | chr13 | 49494211 | ||||||
| chr13:49494228 | A | G | 1 | a0002c0003t0035 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2379A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2379 | chr13 | 49494228 | ||||||
| chr13:49494241 | T | G | 1 | a0001c0001t0041 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2392T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2392 | chr13 | 49494241 | ||||||
| chr13:49494251 | G | A | 19 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0010 others(16): Show |
171 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*2402G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2402 | chr13 | 49494251 | ||||||
| chr13:49494434 | G | A | 1 | a0001c0001t0017 | 3 | HG01243.hp2 HG02922.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2585G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2585 | chr13 | 49494434 | ||||||
| chr13:49494488 | T | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2639T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2639 | chr13 | 49494488 | ||||||
| chr13:49494489 | A | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2640A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2640 | chr13 | 49494489 | ||||||
| chr13:49494490 | C | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2641C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2641 | chr13 | 49494490 | ||||||
| chr13:49494491 | T | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2642T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2642 | chr13 | 49494491 | ||||||
| chr13:49494492 | A | G | 47 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(44): Show |
351 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(348): Show |
3_prime_UTR_variant | MODIFIER | c.*2643A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2643 | chr13 | 49494492 | ||||||
| chr13:49494493 | T | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2644T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2644 | chr13 | 49494493 | ||||||
| chr13:49494495 | A | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2646A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2646 | chr13 | 49494495 | ||||||
| chr13:49494497 | C | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2648C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2648 | chr13 | 49494497 | ||||||
| chr13:49494497 | C | T | 1 | a0003c0004t0032 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2648C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2648 | chr13 | 49494497 | ||||||
| chr13:49494498 | T | C | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2649T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2649 | chr13 | 49494498 | ||||||
| chr13:49494499 | G | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2650G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2650 | chr13 | 49494499 | ||||||
| chr13:49494502 | A | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2653A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2653 | chr13 | 49494502 | ||||||
| chr13:49494507 | G | A | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2658G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2658 | chr13 | 49494507 | ||||||
| chr13:49494511 | A | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2662A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2662 | chr13 | 49494511 | ||||||
| chr13:49494517 | T | TTGGTTTA others(4): Show |
1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2668_*2669insTGGT others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2669 | chr13 | 49494517 | ||||||
| chr13:49494525 | T | A | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2676T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2676 | chr13 | 49494525 | ||||||
| chr13:49494546 | A | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2697A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2697 | chr13 | 49494546 | ||||||
| chr13:49494548 | C | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2699C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2699 | chr13 | 49494548 | ||||||
| chr13:49494551 | G | C | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2702G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2702 | chr13 | 49494551 | ||||||
| chr13:49494552 | C | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2703C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2703 | chr13 | 49494552 | ||||||
| chr13:49494553 | T | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2704T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2704 | chr13 | 49494553 | ||||||
| chr13:49494584 | A | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2735A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2735 | chr13 | 49494584 | ||||||
| chr13:49494594 | C | A | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2745C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2745 | chr13 | 49494594 | ||||||
| chr13:49494596 | T | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2747T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2747 | chr13 | 49494596 | ||||||
| chr13:49494644 | A | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2795A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2795 | chr13 | 49494644 | ||||||
| chr13:49494647 | A | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2798A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2798 | chr13 | 49494647 | ||||||
| chr13:49494650 | A | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2801A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2801 | chr13 | 49494650 | ||||||
| chr13:49494697 | C | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2848C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2848 | chr13 | 49494697 | ||||||
| chr13:49494709 | T | A | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2860T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2860 | chr13 | 49494709 | ||||||
| chr13:49494712 | T | A | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2863T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2863 | chr13 | 49494712 | ||||||
| chr13:49494745 | C | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2896C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2896 | chr13 | 49494745 | ||||||
| chr13:49494761 | A | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2912A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2912 | chr13 | 49494761 | ||||||
| chr13:49494762 | T | A | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2913T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2913 | chr13 | 49494762 | ||||||
| chr13:49494765 | T | C | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2916T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2916 | chr13 | 49494765 | ||||||
| chr13:49494766 | C | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2917C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2917 | chr13 | 49494766 | ||||||
| chr13:49494767 | T | A | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2918T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2918 | chr13 | 49494767 | ||||||
| chr13:49494768 | C | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2919C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2919 | chr13 | 49494768 | ||||||
| chr13:49494796 | T | A | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2947T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2947 | chr13 | 49494796 | ||||||
| chr13:49494797 | C | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2948C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2948 | chr13 | 49494797 | ||||||
| chr13:49494800 | C | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2951C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2951 | chr13 | 49494800 | ||||||
| chr13:49494801 | T | A | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2952T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2952 | chr13 | 49494801 | ||||||
| chr13:49494803 | T | C | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2954T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2954 | chr13 | 49494803 | ||||||
| chr13:49494804 | A | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2955A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2955 | chr13 | 49494804 | ||||||
| chr13:49494837 | C | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2988C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2988 | chr13 | 49494837 | ||||||
| chr13:49494841 | T | A | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2992T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2992 | chr13 | 49494841 | ||||||
| chr13:49494843 | A | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2994A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2994 | chr13 | 49494843 | ||||||
| chr13:49494846 | C | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2997C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 2997 | chr13 | 49494846 | ||||||
| chr13:49494849 | C | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3000C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 3000 | chr13 | 49494849 | ||||||
| chr13:49494857 | C | G | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3008C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 3008 | chr13 | 49494857 | ||||||
| chr13:49494861 | A | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3012A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 3012 | chr13 | 49494861 | ||||||
| chr13:49494865 | A | T | 1 | a0008c0011t0039 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3016A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 3016 | chr13 | 49494865 | ||||||
| chr13:49494940 | C | T | 1 | a0001c0002t0030 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3091C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 14/14 | 3091 | chr13 | 49494940 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49444985 | G | T | 1 | a0001c0002t0004g0375 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-342+128G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49444985 | |||||||
| chr13:49445012 | A | T | 1 | a0003c0004t0005g0374 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-342+155A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445012 | |||||||
| chr13:49445128 | G | C | 1 | a0002c0003t0033g0023 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-342+271G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445128 | |||||||
| chr13:49445144 | C | G | 49 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0004g0330 others(46): Show |
50 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.-342+287C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445144 | |||||||
| chr13:49445240 | T | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
187 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.-342+383T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445240 | |||||||
| chr13:49445471 | C | T | 1 | a0001c0001t0010g0193 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-342+614C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445471 | |||||||
| chr13:49445681 | C | A | 5 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-342+824C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445681 | |||||||
| chr13:49445936 | C | CAA | 112 | a0001c0001t0001g0192 a0001c0001t0005g0332 a0001c0001t0005g0333 others(109): Show |
122 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.-342+1094_-342+109 others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49445936 | ||||||
| chr13:49445936 | C | CAAA | 169 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(166): Show |
181 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(178): Show |
intron_variant | MODIFIER | c.-342+1093_-342+109 others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49445936 | ||||||
| chr13:49445936 | C | CAAAA | 43 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(40): Show |
44 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.-342+1092_-342+109 others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49445936 | ||||||
| chr13:49445972 | G | T | 3 | a0001c0001t0013g0190 a0001c0001t0027g0189 a0001c0001t0028g0191 |
3 | HG01884.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-342+1115G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445972 | |||||||
| chr13:49445986 | A | G | 1 | a0001c0002t0009g0373 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-342+1129A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49445986 | |||||||
| chr13:49446144 | C | G | 153 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
161 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(158): Show |
intron_variant | MODIFIER | c.-342+1287C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49446144 | |||||||
| chr13:49446280 | G | A | 2 | a0001c0002t0003g0229 a0001c0002t0003g0230 |
2 | HG01192.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-342+1423G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49446280 | |||||||
| chr13:49446783 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-342+1926C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49446783 | |||||||
| chr13:49447123 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-342+2266A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447123 | |||||||
| chr13:49447314 | A | G | 4 | a0001c0002t0012g0016 a0001c0002t0012g0280 a0001c0002t0012g0281 others(1): Show |
5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-342+2457A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447314 | |||||||
| chr13:49447406 | G | A | 28 | a0001c0002t0004g0220 a0003c0004t0005g0006 a0003c0004t0005g0200 others(25): Show |
30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.-342+2549G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447406 | |||||||
| chr13:49447415 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-342+2558T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447415 | |||||||
| chr13:49447470 | G | A | 2 | a0002c0003t0002g0283 a0002c0003t0002g0284 |
2 | NA18947.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-342+2613G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447470 | |||||||
| chr13:49447513 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-342+2656G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447513 | |||||||
| chr13:49447563 | T | A | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG00140.hp2 HG01346.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-342+2706T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447563 | |||||||
| chr13:49447918 | G | A | 1 | a0001c0002t0003g0232 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-342+3061G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447918 | |||||||
| chr13:49447953 | G | C | 320 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(317): Show |
343 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(340): Show |
intron_variant | MODIFIER | c.-342+3096G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447953 | |||||||
| chr13:49447973 | A | G | 7 | a0001c0002t0007g0011 a0001c0002t0029g0228 a0003c0004t0018g0196 others(4): Show |
8 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-342+3116A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49447973 | |||||||
| chr13:49448325 | A | G | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG00438.hp2 NA18960.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.-341-3228A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448325 | |||||||
| chr13:49448490 | C | T | 2 | a0002c0003t0002g0084 a0002c0003t0002g0085 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-341-3063C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448490 | |||||||
| chr13:49448628 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-341-2925G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448628 | |||||||
| chr13:49448707 | C | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG00609.hp1 HG01255.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-341-2846C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448707 | |||||||
| chr13:49448737 | C | T | 28 | a0001c0002t0004g0220 a0003c0004t0005g0006 a0003c0004t0005g0200 others(25): Show |
30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.-341-2816C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448737 | |||||||
| chr13:49448746 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0172 others(4): Show |
8 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-341-2807A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448746 | |||||||
| chr13:49448810 | C | T | 1 | a0002c0003t0002g0328 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-341-2743C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448810 | |||||||
| chr13:49448846 | A | G | 2 | a0001c0001t0010g0170 a0001c0001t0010g0171 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-341-2707A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448846 | |||||||
| chr13:49448921 | G | A | 1 | a0001c0002t0026g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-341-2632G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49448921 | |||||||
| chr13:49449000 | C | A | 5 | a0002c0003t0008g0017 a0002c0003t0008g0287 a0002c0003t0008g0288 others(2): Show |
6 | HG00280.hp1 HG01069.hp1 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.-341-2553C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449000 | |||||||
| chr13:49449031 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-341-2522G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449031 | |||||||
| chr13:49449346 | G | T | 1 | a0001c0008t0005g0009 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-341-2207G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449346 | |||||||
| chr13:49449438 | A | G | 1 | a0001c0001t0028g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-341-2115A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449438 | |||||||
| chr13:49449943 | G | A | 5 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-341-1610G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449943 | |||||||
| chr13:49449946 | T | A | 5 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-341-1607T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49449946 | |||||||
| chr13:49450088 | C | T | 1 | a0001c0002t0004g0372 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-341-1465C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450088 | |||||||
| chr13:49450718 | C | G | 63 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(60): Show |
72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-341-835C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450718 | |||||||
| chr13:49450735 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.-341-818A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450735 | |||||||
| chr13:49450741 | A | G | 46 | a0001c0002t0004g0330 a0001c0002t0004g0331 a0001c0002t0004g0334 others(43): Show |
47 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.-341-812A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450741 | |||||||
| chr13:49450851 | A | G | 2 | a0001c0002t0007g0011 a0001c0002t0029g0228 |
3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-341-702A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450851 | |||||||
| chr13:49450866 | T | G | 1 | a0001c0008t0005g0009 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-341-687T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450866 | |||||||
| chr13:49450903 | A | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(17): Show |
22 | HG00621.hp2 HG01975.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.-341-650A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450903 | |||||||
| chr13:49450918 | CTAAA | C | 3 | a0001c0002t0003g0277 a0001c0002t0003g0278 a0001c0002t0003g0279 |
3 | HG01981.hp1 HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.-341-632_-341-629d others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49450918 | ||||||
| chr13:49450941 | ATAT | A | 63 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(60): Show |
72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-341-606_-341-604d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49450941 | ||||||
| chr13:49450945 | TATTA | T | 2 | a0001c0002t0007g0011 a0001c0002t0029g0228 |
3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-341-601_-341-598d others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49450945 | ||||||
| chr13:49450966 | AAATTT | A | 63 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(60): Show |
72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-341-582_-341-578d others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49450966 | ||||||
| chr13:49450977 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0179 |
3 | HG01255.hp1 HG01496.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.-341-576T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49450977 | |||||||
| chr13:49451006 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-341-547C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451006 | |||||||
| chr13:49451066 | G | A | 2 | a0003c0004t0020g0194 a0007c0009t0020g0195 |
2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-341-487G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451066 | |||||||
| chr13:49451103 | AAAATT | A | 7 | a0001c0002t0003g0012 a0001c0002t0003g0233 a0001c0002t0003g0235 others(4): Show |
10 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-341-445_-341-441d others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451103 | ||||||
| chr13:49451195 | G | A | 29 | a0001c0002t0004g0220 a0003c0004t0005g0006 a0003c0004t0005g0200 others(26): Show |
31 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.-341-358G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451195 | |||||||
| chr13:49451204 | A | C | 2 | a0001c0002t0007g0011 a0001c0002t0029g0228 |
3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-341-349A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451204 | |||||||
| chr13:49451336 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 |
3 | HG01515.hp2 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-341-217T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451336 | |||||||
| chr13:49451359 | T | A | 319 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(316): Show |
342 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(339): Show |
intron_variant | MODIFIER | c.-341-194T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451359 | |||||||
| chr13:49451478 | C | CAT | 31 | a0001c0001t0013g0060 a0001c0001t0013g0061 a0001c0001t0013g0063 others(28): Show |
32 | HG00140.hp2 HG00280.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-341-48_-341-47dup others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | ||||||
| chr13:49451478 | C | CATAT | 9 | a0001c0001t0001g0092 a0001c0001t0021g0059 a0001c0002t0004g0330 others(6): Show |
10 | HG00733.hp2 HG01978.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.-341-50_-341-47dup others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | ||||||
| chr13:49451478 | CAT | C | 89 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0058 others(86): Show |
96 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-341-48_-341-47del others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | ||||||
| chr13:49451478 | CATAT | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(161): Show |
179 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.-341-50_-341-47del others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | ||||||
| chr13:49451478 | CATATAT | C | 22 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0001t0013g0190 others(19): Show |
25 | HG00639.hp1 HG00741.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.-341-52_-341-47del others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | ||||||
| chr13:49451478 | CATATATA others(1): Show |
C | 4 | a0001c0001t0028g0191 a0001c0002t0012g0282 a0002c0003t0002g0084 others(1): Show |
4 | HG03209.hp2 HG03579.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-341-54_-341-47del others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | ||||||
| chr13:49451478 | CATATATA others(3): Show |
C | 5 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-341-56_-341-47del others(10): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | ||||||
| chr13:49451478 | CATATATA others(5): Show |
C | 1 | a0001c0002t0008g0276 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-341-58_-341-47del others(12): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr13 | 49451478 | ||||||
| chr13:49451485 | A | G | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-341-68A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 1/13 | chr13 | 49451485 | |||||||
| chr13:49452110 | CT | C | 31 | a0001c0002t0004g0220 a0003c0004t0005g0006 a0003c0004t0005g0200 others(28): Show |
33 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.16+213delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49452110 | ||||||
| chr13:49452149 | T | C | 1 | a0001c0002t0026g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.16+240T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452149 | |||||||
| chr13:49452200 | C | T | 2 | a0002c0003t0002g0084 a0002c0003t0002g0085 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16+291C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452200 | |||||||
| chr13:49452525 | G | A | 1 | a0001c0002t0026g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.16+616G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452525 | |||||||
| chr13:49452656 | C | T | 5 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+747C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452656 | |||||||
| chr13:49452758 | A | G | 22 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0096 others(19): Show |
23 | HG00438.hp1 HG00558.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.16+849A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452758 | |||||||
| chr13:49452812 | C | T | 2 | a0003c0004t0020g0194 a0007c0009t0020g0195 |
2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.16+903C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452812 | |||||||
| chr13:49452844 | A | G | 1 | a0007c0009t0020g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.16+935A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452844 | |||||||
| chr13:49452928 | G | A | 1 | a0001c0001t0027g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.16+1019G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49452928 | |||||||
| chr13:49453059 | A | G | 1 | a0002c0003t0002g0324 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.16+1150A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453059 | |||||||
| chr13:49453134 | C | A | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
348 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(345): Show |
intron_variant | MODIFIER | c.16+1225C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453134 | |||||||
| chr13:49453197 | T | C | 63 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(60): Show |
72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.16+1288T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453197 | |||||||
| chr13:49453302 | T | C | 2 | a0002c0003t0002g0084 a0002c0003t0002g0085 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16+1393T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453302 | |||||||
| chr13:49453303 | C | CT | 29 | a0001c0001t0001g0053 a0001c0002t0004g0220 a0003c0004t0005g0006 others(26): Show |
31 | HG00280.hp2 HG01109.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.16+1405dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49453303 | ||||||
| chr13:49453513 | G | C | 1 | a0001c0002t0012g0282 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.16+1604G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453513 | |||||||
| chr13:49453566 | G | C | 48 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0004g0330 others(45): Show |
49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+1657G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453566 | |||||||
| chr13:49453627 | C | T | 5 | a0001c0002t0004g0331 a0001c0002t0004g0369 a0001c0002t0004g0370 others(2): Show |
5 | HG00642.hp1 HG02602.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+1718C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453627 | |||||||
| chr13:49453710 | C | T | 48 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0004g0330 others(45): Show |
49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+1801C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49453710 | |||||||
| chr13:49453870 | G | GTA | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
170 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.16+1974_16+1975dup others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49453870 | ||||||
| chr13:49454174 | G | T | 1 | a0001c0001t0001g0136 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.16+2265G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454174 | |||||||
| chr13:49454248 | A | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0192 |
2 | HG01358.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.16+2339A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454248 | |||||||
| chr13:49454251 | T | A | 1 | a0001c0002t0014g0242 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.16+2342T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454251 | |||||||
| chr13:49454363 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
316 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.16+2454T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454363 | |||||||
| chr13:49454553 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.16+2644G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454553 | |||||||
| chr13:49454749 | A | G | 1 | a0001c0014t0003g0264 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.16+2840A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454749 | |||||||
| chr13:49454900 | C | T | 48 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0004g0330 others(45): Show |
49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+2991C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49454900 | |||||||
| chr13:49455145 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.16+3236C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455145 | |||||||
| chr13:49455244 | G | A | 48 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0004g0330 others(45): Show |
49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+3335G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455244 | |||||||
| chr13:49455296 | A | G | 1 | a0001c0001t0023g0133 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.16+3387A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455296 | |||||||
| chr13:49455339 | G | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
316 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.16+3430G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455339 | |||||||
| chr13:49455446 | C | T | 2 | a0003c0004t0018g0197 a0003c0004t0018g0198 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.16+3537C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455446 | |||||||
| chr13:49455462 | G | T | 4 | a0001c0002t0012g0016 a0001c0002t0012g0280 a0001c0002t0012g0281 others(1): Show |
5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+3553G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455462 | |||||||
| chr13:49455527 | T | G | 1 | a0001c0001t0013g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.16+3618T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455527 | |||||||
| chr13:49455549 | C | T | 1 | a0003c0004t0031g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.16+3640C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455549 | |||||||
| chr13:49455648 | C | T | 48 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0004g0330 others(45): Show |
49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+3739C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455648 | |||||||
| chr13:49455652 | A | T | 1 | a0001c0002t0024g0371 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.16+3743A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455652 | |||||||
| chr13:49455755 | A | G | 1 | a0001c0002t0009g0367 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.16+3846A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455755 | |||||||
| chr13:49455785 | CAAAA | C | 28 | a0001c0002t0004g0220 a0003c0004t0005g0006 a0003c0004t0005g0200 others(25): Show |
30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.16+3882_16+3885del others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49455785 | ||||||
| chr13:49455805 | TA | T | 8 | a0001c0001t0007g0003 a0001c0001t0007g0064 a0001c0001t0007g0078 others(5): Show |
10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.16+3897delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455805 | |||||||
| chr13:49455840 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
316 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.16+3931T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455840 | |||||||
| chr13:49455864 | A | G | 2 | a0002c0003t0002g0084 a0002c0003t0002g0085 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16+3955A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455864 | |||||||
| chr13:49455909 | G | A | 2 | a0002c0003t0002g0084 a0002c0003t0002g0085 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.16+4000G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455909 | |||||||
| chr13:49455971 | G | T | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.16+4062G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49455971 | |||||||
| chr13:49456032 | G | A | 1 | a0001c0002t0022g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.17-4075G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456032 | |||||||
| chr13:49456129 | C | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
170 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.17-3978C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456129 | |||||||
| chr13:49456210 | C | A | 4 | a0001c0002t0012g0016 a0001c0002t0012g0280 a0001c0002t0012g0281 others(1): Show |
5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-3897C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456210 | |||||||
| chr13:49456528 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.17-3579G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456528 | |||||||
| chr13:49456566 | G | T | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.17-3541G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456566 | |||||||
| chr13:49456688 | T | C | 3 | a0001c0002t0004g0015 a0001c0002t0004g0265 a0001c0002t0004g0266 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-3419T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456688 | |||||||
| chr13:49456850 | G | A | 2 | a0002c0003t0002g0084 a0002c0003t0002g0085 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.17-3257G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456850 | |||||||
| chr13:49456892 | G | A | 1 | a0003c0004t0005g0205 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.17-3215G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456892 | |||||||
| chr13:49456926 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.17-3181G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49456926 | |||||||
| chr13:49457034 | G | T | 39 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(36): Show |
46 | HG00408.hp1 HG00642.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.17-3073G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457034 | |||||||
| chr13:49457215 | C | CCT | 3 | a0001c0002t0004g0015 a0001c0002t0004g0265 a0001c0002t0004g0266 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-2892_17-2891ins others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457215 | |||||||
| chr13:49457215 | C | CT | 9 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0004g0375 others(6): Show |
9 | HG01109.hp1 HG02015.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.17-2877dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457215 | ||||||
| chr13:49457215 | C | CTT | 149 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(146): Show |
161 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.17-2878_17-2877dup others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457215 | ||||||
| chr13:49457216 | T | TTC | 157 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
167 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.17-2890_17-2889ins others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457216 | ||||||
| chr13:49457217 | T | TC | 3 | a0001c0001t0001g0033 a0001c0001t0001g0137 a0001c0001t0010g0054 |
3 | HG02647.hp2 HG03239.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.17-2890_17-2889ins others(1): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457217 | |||||||
| chr13:49457261 | G | A | 1 | a0003c0004t0005g0206 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.17-2846G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457261 | |||||||
| chr13:49457287 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.17-2820T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457287 | |||||||
| chr13:49457292 | T | G | 1 | a0003c0004t0005g0207 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.17-2815T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457292 | |||||||
| chr13:49457306 | A | AT | 8 | a0001c0001t0007g0003 a0001c0001t0007g0064 a0001c0001t0007g0078 others(5): Show |
10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.17-2797dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457306 | ||||||
| chr13:49457400 | A | AG | 325 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(322): Show |
348 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(345): Show |
intron_variant | MODIFIER | c.17-2707_17-2706ins others(1): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457400 | |||||||
| chr13:49457435 | C | CT | 16 | a0001c0001t0001g0092 a0002c0003t0002g0293 a0002c0003t0002g0318 others(13): Show |
17 | HG00280.hp1 HG00609.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.17-2654dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457435 | ||||||
| chr13:49457435 | CT | C | 276 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(273): Show |
297 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.17-2654delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457435 | ||||||
| chr13:49457435 | CTT | C | 8 | a0001c0001t0001g0137 a0001c0001t0043g0138 a0001c0002t0003g0248 others(5): Show |
8 | HG01074.hp2 HG02897.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.17-2655_17-2654del others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr13 | 49457435 | ||||||
| chr13:49457470 | G | A | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.17-2637G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457470 | |||||||
| chr13:49457474 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
316 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.17-2633C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457474 | |||||||
| chr13:49457591 | G | A | 1 | a0003c0004t0031g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.17-2516G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457591 | |||||||
| chr13:49457732 | A | G | 104 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(101): Show |
108 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.17-2375A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457732 | |||||||
| chr13:49457925 | A | G | 28 | a0001c0002t0004g0220 a0003c0004t0005g0006 a0003c0004t0005g0200 others(25): Show |
30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.17-2182A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49457925 | |||||||
| chr13:49458157 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(155): Show |
168 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.17-1950C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458157 | |||||||
| chr13:49458340 | G | A | 63 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0004g0330 others(60): Show |
64 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.17-1767G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458340 | |||||||
| chr13:49458368 | C | G | 1 | a0003c0004t0018g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.17-1739C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458368 | |||||||
| chr13:49458463 | C | T | 1 | a0004c0005t0006g0077 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.17-1644C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458463 | |||||||
| chr13:49458653 | G | T | 1 | a0003c0004t0005g0224 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.17-1454G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458653 | |||||||
| chr13:49458719 | G | A | 28 | a0001c0002t0004g0220 a0003c0004t0005g0006 a0003c0004t0005g0200 others(25): Show |
30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.17-1388G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458719 | |||||||
| chr13:49458838 | C | T | 2 | a0002c0003t0002g0084 a0002c0003t0002g0085 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.17-1269C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458838 | |||||||
| chr13:49458960 | G | A | 1 | a0003c0004t0031g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.17-1147G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458960 | |||||||
| chr13:49458965 | G | C | 49 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0004g0330 others(46): Show |
50 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.17-1142G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458965 | |||||||
| chr13:49458992 | C | A | 2 | a0002c0003t0002g0305 a0002c0003t0002g0323 |
2 | HG02056.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.17-1115C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49458992 | |||||||
| chr13:49459007 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.17-1100C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459007 | |||||||
| chr13:49459052 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(144): Show |
155 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.17-1055G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459052 | |||||||
| chr13:49459530 | T | A | 3 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 |
3 | HG01109.hp1 HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.17-577T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459530 | |||||||
| chr13:49459741 | C | T | 5 | a0003c0004t0005g0204 a0003c0004t0005g0208 a0003c0004t0005g0221 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-366C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459741 | |||||||
| chr13:49459767 | T | C | 3 | a0001c0002t0004g0015 a0001c0002t0004g0265 a0001c0002t0004g0266 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-340T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459767 | |||||||
| chr13:49459804 | T | C | 11 | a0001c0002t0003g0001 a0001c0002t0003g0232 a0001c0002t0003g0233 others(8): Show |
15 | NA18612.hp1 NA18946.hp2 NA18953.hp2 others(12): Show |
intron_variant | MODIFIER | c.17-303T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459804 | |||||||
| chr13:49459894 | A | T | 1 | a0001c0001t0013g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.17-213A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49459894 | |||||||
| chr13:49460001 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.17-106T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 2/13 | chr13 | 49460001 | |||||||
| chr13:49460256 | A | G | 2 | a0001c0002t0004g0340 a0001c0002t0004g0342 |
2 | NA19060.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.142+24A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460256 | |||||||
| chr13:49460261 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.142+29T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460261 | |||||||
| chr13:49460548 | C | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
171 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.142+316C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460548 | |||||||
| chr13:49460587 | T | G | 8 | a0001c0001t0013g0060 a0001c0001t0013g0061 a0001c0001t0013g0063 others(5): Show |
8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+355T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460587 | |||||||
| chr13:49460606 | G | C | 4 | a0004c0005t0006g0066 a0004c0005t0006g0067 a0004c0005t0006g0068 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.142+374G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460606 | |||||||
| chr13:49460646 | A | AT | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(118): Show |
126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.142+420dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr13 | 49460646 | ||||||
| chr13:49460655 | A | T | 1 | a0002c0003t0034g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.142+423A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460655 | |||||||
| chr13:49460749 | T | C | 28 | a0001c0002t0004g0220 a0003c0004t0005g0006 a0003c0004t0005g0200 others(25): Show |
30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.143-348T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460749 | |||||||
| chr13:49460906 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
316 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.143-191T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460906 | |||||||
| chr13:49460912 | G | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
316 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(313): Show |
intron_variant | MODIFIER | c.143-185G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49460912 | |||||||
| chr13:49461015 | G | C | 160 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
170 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.143-82G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49461015 | |||||||
| chr13:49461072 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
171 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.143-25G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 3/13 | chr13 | 49461072 | |||||||
| chr13:49461276 | T | G | 1 | a0001c0008t0005g0009 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.208+114T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461276 | |||||||
| chr13:49461293 | C | T | 29 | a0001c0002t0004g0220 a0003c0004t0005g0006 a0003c0004t0005g0200 others(26): Show |
31 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.208+131C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461293 | |||||||
| chr13:49461377 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.208+215A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461377 | |||||||
| chr13:49461398 | G | A | 7 | a0001c0001t0010g0054 a0001c0001t0010g0159 a0001c0001t0010g0160 others(4): Show |
7 | HG01975.hp2 HG02055.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+236G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461398 | |||||||
| chr13:49461660 | G | A | 5 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+498G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461660 | |||||||
| chr13:49461944 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.208+782G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49461944 | |||||||
| chr13:49462216 | T | C | 1 | a0002c0003t0002g0308 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.208+1054T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462216 | |||||||
| chr13:49462262 | C | G | 64 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0090 others(61): Show |
68 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.208+1100C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462262 | |||||||
| chr13:49462426 | T | C | 1 | a0001c0002t0030g0368 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.208+1264T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462426 | |||||||
| chr13:49462546 | C | A | 3 | a0001c0001t0013g0190 a0001c0001t0027g0189 a0001c0001t0028g0191 |
3 | HG01884.hp2 HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.208+1384C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462546 | |||||||
| chr13:49462562 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.208+1400A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462562 | |||||||
| chr13:49462574 | T | C | 1 | a0001c0008t0005g0009 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.208+1412T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462574 | |||||||
| chr13:49462654 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.208+1492A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462654 | |||||||
| chr13:49462698 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0167 |
2 | HG02165.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.208+1536A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462698 | |||||||
| chr13:49462731 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.208+1569C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49462731 | |||||||
| chr13:49463130 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(17): Show |
22 | HG00621.hp2 HG01975.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.208+1968C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463130 | |||||||
| chr13:49463162 | C | T | 2 | a0002c0003t0002g0305 a0002c0003t0002g0323 |
2 | HG02056.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.208+2000C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463162 | |||||||
| chr13:49463171 | AT | A | 285 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(282): Show |
305 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.208+2021delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49463171 | ||||||
| chr13:49463186 | A | G | 14 | a0001c0002t0008g0243 a0001c0002t0008g0269 a0001c0002t0008g0270 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+2024A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463186 | |||||||
| chr13:49463290 | C | T | 2 | a0001c0001t0005g0332 a0001c0001t0005g0333 |
2 | HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.208+2128C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463290 | |||||||
| chr13:49463369 | G | A | 1 | a0001c0002t0012g0282 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.208+2207G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463369 | |||||||
| chr13:49463531 | T | C | 8 | a0001c0001t0013g0060 a0001c0001t0013g0061 a0001c0001t0013g0063 others(5): Show |
8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+2369T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463531 | |||||||
| chr13:49463669 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.208+2507G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463669 | |||||||
| chr13:49463727 | C | A | 63 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(60): Show |
72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.208+2565C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463727 | |||||||
| chr13:49463728 | CACT | C | 7 | a0001c0002t0007g0011 a0001c0002t0029g0228 a0003c0004t0018g0196 others(4): Show |
8 | HG01109.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.208+2567_208+2569d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463728 | |||||||
| chr13:49463777 | G | T | 1 | a0001c0001t0013g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208+2615G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463777 | |||||||
| chr13:49463820 | T | C | 171 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
182 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.208+2658T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463820 | |||||||
| chr13:49463944 | G | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(133): Show |
143 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.208+2782G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49463944 | |||||||
| chr13:49464073 | C | T | 30 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0002t0004g0220 others(27): Show |
32 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(29): Show |
intron_variant | MODIFIER | c.208+2911C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464073 | |||||||
| chr13:49464219 | T | C | 5 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.208+3057T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464219 | |||||||
| chr13:49464221 | C | T | 60 | a0001c0002t0004g0330 a0001c0002t0004g0331 a0001c0002t0004g0334 others(57): Show |
61 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.208+3059C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464221 | |||||||
| chr13:49464252 | A | T | 2 | a0001c0002t0007g0011 a0001c0002t0029g0228 |
3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.208+3090A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464252 | |||||||
| chr13:49464284 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.208+3122T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464284 | |||||||
| chr13:49464357 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.208+3195T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464357 | |||||||
| chr13:49464394 | C | G | 1 | a0001c0001t0027g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.208+3232C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464394 | |||||||
| chr13:49464521 | C | T | 14 | a0001c0002t0008g0243 a0001c0002t0008g0269 a0001c0002t0008g0270 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.209-3343C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464521 | |||||||
| chr13:49464531 | C | T | 3 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0008t0005g0009 |
4 | HG02717.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-3333C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464531 | |||||||
| chr13:49464594 | C | T | 1 | a0001c0014t0003g0264 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.209-3270C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464594 | |||||||
| chr13:49464704 | A | G | 294 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(291): Show |
315 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(312): Show |
intron_variant | MODIFIER | c.209-3160A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464704 | |||||||
| chr13:49464981 | G | A | 63 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(60): Show |
72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.209-2883G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49464981 | |||||||
| chr13:49465072 | T | TA | 227 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(224): Show |
241 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.209-2778dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49465072 | ||||||
| chr13:49465115 | A | T | 293 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(290): Show |
314 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(311): Show |
intron_variant | MODIFIER | c.209-2749A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465115 | |||||||
| chr13:49465180 | A | C | 8 | a0001c0001t0013g0060 a0001c0001t0013g0061 a0001c0001t0013g0063 others(5): Show |
8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-2684A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465180 | |||||||
| chr13:49465211 | T | C | 1 | a0002c0003t0015g0317 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.209-2653T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465211 | |||||||
| chr13:49465237 | G | A | 16 | a0001c0001t0007g0003 a0001c0001t0007g0064 a0001c0001t0007g0078 others(13): Show |
18 | HG01074.hp1 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.209-2627G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465237 | |||||||
| chr13:49465372 | A | G | 31 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0002t0004g0220 others(28): Show |
33 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(30): Show |
intron_variant | MODIFIER | c.209-2492A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465372 | |||||||
| chr13:49465539 | A | AT | 6 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0128 others(3): Show |
6 | HG01517.hp1 HG01981.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.209-2311dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49465539 | ||||||
| chr13:49465600 | G | A | 1 | a0003c0004t0005g0206 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.209-2264G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465600 | |||||||
| chr13:49465629 | C | T | 2 | a0001c0001t0001g0041 a0002c0003t0034g0306 |
2 | HG02280.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.209-2235C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465629 | |||||||
| chr13:49465662 | G | A | 1 | a0001c0002t0008g0269 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.209-2202G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465662 | |||||||
| chr13:49465785 | C | T | 10 | a0001c0002t0009g0021 a0001c0002t0009g0022 a0001c0002t0009g0362 others(7): Show |
11 | HG00558.hp2 HG02132.hp1 NA18973.hp2 others(8): Show |
intron_variant | MODIFIER | c.209-2079C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49465785 | |||||||
| chr13:49466160 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.209-1704G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466160 | |||||||
| chr13:49466254 | G | C | 17 | a0001c0001t0001g0096 a0001c0001t0001g0137 a0001c0001t0001g0139 others(14): Show |
17 | HG00438.hp1 HG02074.hp2 NA18612.hp2 others(14): Show |
intron_variant | MODIFIER | c.209-1610G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466254 | |||||||
| chr13:49466438 | T | TA | 35 | a0001c0001t0001g0139 a0001c0001t0037g0102 a0001c0002t0004g0220 others(32): Show |
37 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.209-1410dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466438 | ||||||
| chr13:49466438 | TA | T | 14 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0002t0004g0370 others(11): Show |
15 | HG02109.hp1 HG02257.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.209-1410delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466438 | ||||||
| chr13:49466457 | T | G | 326 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(323): Show |
349 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(346): Show |
intron_variant | MODIFIER | c.209-1407T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466457 | |||||||
| chr13:49466573 | G | A | 1 | a0002c0003t0002g0309 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.209-1291G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466573 | |||||||
| chr13:49466684 | G | A | 3 | a0001c0002t0004g0343 a0001c0002t0004g0344 a0001c0002t0004g0345 |
3 | HG02155.hp1 NA19009.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.209-1180G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466684 | |||||||
| chr13:49466811 | C | CT | 91 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(88): Show |
103 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.209-1033dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466811 | ||||||
| chr13:49466811 | C | CTT | 188 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(185): Show |
197 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.209-1034_209-1033d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466811 | ||||||
| chr13:49466811 | C | CTTT | 11 | a0001c0001t0001g0035 a0001c0001t0001g0058 a0001c0001t0001g0100 others(8): Show |
11 | HG01123.hp2 HG02055.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.209-1035_209-1033d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466811 | ||||||
| chr13:49466811 | CT | C | 28 | a0001c0002t0004g0220 a0003c0004t0005g0006 a0003c0004t0005g0200 others(25): Show |
30 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.209-1033delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49466811 | ||||||
| chr13:49466872 | C | T | 1 | a0003c0004t0031g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.209-992C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49466872 | |||||||
| chr13:49467082 | G | C | 1 | a0001c0001t0027g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.209-782G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467082 | |||||||
| chr13:49467265 | C | T | 46 | a0001c0002t0004g0330 a0001c0002t0004g0331 a0001c0002t0004g0334 others(43): Show |
47 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.209-599C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467265 | |||||||
| chr13:49467366 | C | T | 2 | a0001c0001t0001g0123 a0003c0004t0018g0196 |
2 | HG02895.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.209-498C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467366 | |||||||
| chr13:49467398 | CA | C | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
346 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.209-457delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr13 | 49467398 | ||||||
| chr13:49467675 | T | G | 1 | a0001c0002t0007g0011 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.209-189T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467675 | |||||||
| chr13:49467791 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.209-73A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467791 | |||||||
| chr13:49467809 | T | C | 1 | a0003c0004t0005g0209 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.209-55T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 4/13 | chr13 | 49467809 | |||||||
| chr13:49467974 | T | C | 1 | a0002c0003t0002g0292 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.305+14T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49467974 | |||||||
| chr13:49468348 | T | G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(135): Show |
145 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.305+388T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468348 | |||||||
| chr13:49468590 | A | G | 8 | a0001c0001t0013g0060 a0001c0001t0013g0061 a0001c0001t0013g0063 others(5): Show |
8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.305+630A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468590 | |||||||
| chr13:49468594 | T | C | 3 | a0001c0002t0019g0227 a0001c0002t0019g0267 a0001c0002t0019g0275 |
3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.305+634T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468594 | |||||||
| chr13:49468614 | T | TGTTACCC others(309): Show |
1 | a0001c0014t0003g0264 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.305+668_305+669ins others(316): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(319): Show |
1 | a0001c0002t0026g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.305+668_305+669ins others(326): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(319): Show |
12 | a0001c0002t0008g0243 a0001c0002t0008g0269 a0001c0002t0008g0270 others(9): Show |
12 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.305+668_305+669ins others(326): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(320): Show |
2 | a0001c0002t0008g0273 a0001c0002t0008g0274 |
2 | HG00741.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.305+668_305+669ins others(327): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(322): Show |
3 | a0004c0005t0006g0066 a0004c0005t0006g0067 a0004c0005t0006g0068 |
3 | HG01243.hp1 HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.305+668_305+669ins others(329): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(323): Show |
1 | a0004c0005t0006g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.305+668_305+669ins others(330): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(323): Show |
39 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(36): Show |
46 | HG00408.hp1 HG00642.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.305+668_305+669ins others(330): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(324): Show |
2 | a0001c0002t0003g0229 a0001c0002t0003g0230 |
2 | HG01192.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.305+668_305+669ins others(331): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(325): Show |
2 | a0001c0002t0004g0340 a0001c0002t0004g0342 |
2 | NA19060.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.305+668_305+669ins others(332): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(326): Show |
37 | a0001c0002t0004g0330 a0001c0002t0004g0331 a0001c0002t0004g0334 others(34): Show |
38 | HG00558.hp2 HG02015.hp2 HG02027.hp1 others(35): Show |
intron_variant | MODIFIER | c.305+668_305+669ins others(333): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(327): Show |
17 | a0001c0002t0004g0220 a0001c0002t0004g0343 a0001c0002t0004g0344 others(14): Show |
17 | HG00408.hp2 HG00642.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.305+668_305+669ins others(334): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(328): Show |
1 | a0001c0002t0004g0335 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.305+668_305+669ins others(335): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(335): Show |
2 | a0001c0002t0004g0015 a0001c0002t0004g0265 |
3 | HG02895.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.305+668_305+669ins others(342): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(336): Show |
1 | a0001c0002t0012g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.305+668_305+669ins others(343): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(337): Show |
2 | a0001c0002t0004g0266 a0001c0002t0012g0016 |
3 | HG03453.hp2 HG03471.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.305+668_305+669ins others(344): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468614 | T | TGTTACCC others(338): Show |
2 | a0001c0002t0012g0281 a0001c0002t0012g0282 |
2 | HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.305+668_305+669ins others(345): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468614 | ||||||
| chr13:49468623 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.305+663A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468623 | |||||||
| chr13:49468661 | A | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
173 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.305+701A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468661 | |||||||
| chr13:49468679 | AT | A | 5 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+726delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49468679 | ||||||
| chr13:49468847 | T | C | 47 | a0001c0002t0004g0220 a0001c0002t0004g0330 a0001c0002t0004g0331 others(44): Show |
48 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.305+887T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49468847 | |||||||
| chr13:49469090 | G | A | 27 | a0003c0004t0005g0006 a0003c0004t0005g0200 a0003c0004t0005g0201 others(24): Show |
29 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.305+1130G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469090 | |||||||
| chr13:49469156 | C | T | 2 | a0001c0002t0003g0229 a0001c0002t0003g0230 |
2 | HG01192.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.305+1196C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469156 | |||||||
| chr13:49469278 | C | T | 48 | a0001c0002t0004g0220 a0001c0002t0004g0330 a0001c0002t0004g0331 others(45): Show |
49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.305+1318C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469278 | |||||||
| chr13:49469500 | T | C | 2 | a0001c0002t0007g0011 a0001c0002t0029g0228 |
3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.305+1540T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469500 | |||||||
| chr13:49469684 | A | G | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
346 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.305+1724A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469684 | |||||||
| chr13:49469874 | C | G | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.305+1914C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469874 | |||||||
| chr13:49469938 | C | T | 1 | a0001c0002t0004g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.305+1978C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49469938 | |||||||
| chr13:49470420 | C | G | 1 | a0001c0002t0004g0375 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.305+2460C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470420 | |||||||
| chr13:49470449 | T | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
173 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.305+2489T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470449 | |||||||
| chr13:49470522 | CTT | C | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.305+2563_305+2564d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470522 | |||||||
| chr13:49470539 | T | C | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
346 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.305+2579T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470539 | |||||||
| chr13:49470574 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.305+2614A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470574 | |||||||
| chr13:49470618 | C | T | 1 | a0001c0002t0004g0266 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.305+2658C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470618 | |||||||
| chr13:49470619 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.305+2659A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470619 | |||||||
| chr13:49470845 | A | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(240): Show |
263 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.305+2885A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470845 | |||||||
| chr13:49470847 | A | G | 3 | a0001c0002t0019g0227 a0001c0002t0019g0267 a0001c0002t0019g0275 |
3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.305+2887A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470847 | |||||||
| chr13:49470861 | A | G | 1 | a0001c0001t0007g0083 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.305+2901A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470861 | |||||||
| chr13:49470872 | G | T | 1 | a0001c0001t0013g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.305+2912G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470872 | |||||||
| chr13:49470888 | A | G | 1 | a0001c0002t0004g0361 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.305+2928A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470888 | |||||||
| chr13:49470927 | T | G | 1 | a0001c0001t0013g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.305+2967T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470927 | |||||||
| chr13:49470941 | G | T | 3 | a0001c0002t0019g0227 a0001c0002t0019g0267 a0001c0002t0019g0275 |
3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.305+2981G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49470941 | |||||||
| chr13:49470966 | C | CT | 48 | a0002c0003t0002g0007 a0002c0003t0002g0018 a0002c0003t0002g0019 others(45): Show |
54 | HG00140.hp2 HG00280.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.305+3024dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | ||||||
| chr13:49470966 | C | CTTTCTT | 20 | a0001c0001t0001g0025 a0001c0001t0001g0036 a0001c0001t0001g0052 others(17): Show |
21 | HG00280.hp2 HG01243.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | ||||||
| chr13:49470966 | C | CTTTCTTT | 70 | a0001c0002t0004g0330 a0001c0002t0004g0334 a0001c0002t0004g0337 others(67): Show |
73 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(9): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | ||||||
| chr13:49470966 | C | CTTTCTTT others(3): Show |
94 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(91): Show |
99 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(12): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | ||||||
| chr13:49470966 | C | CTTTCTTT others(4): Show |
18 | a0001c0001t0001g0049 a0001c0001t0001g0057 a0001c0001t0001g0096 others(15): Show |
18 | HG00609.hp1 HG01123.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(13): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | ||||||
| chr13:49470966 | C | CTTTCTTT others(7): Show |
1 | a0001c0001t0001g0132 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.305+3009_305+3010i others(16): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | ||||||
| chr13:49470966 | C | CTTTCTTT others(1): Show |
38 | a0001c0001t0001g0157 a0001c0001t0010g0160 a0001c0001t0013g0060 others(35): Show |
40 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(10): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | ||||||
| chr13:49470966 | C | CTTTCTTT others(2): Show |
65 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(62): Show |
76 | HG00408.hp1 HG00621.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(11): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | ||||||
| chr13:49470966 | C | CTTTCTTT others(3): Show |
12 | a0001c0001t0001g0169 a0001c0001t0007g0078 a0001c0001t0007g0082 others(9): Show |
13 | HG00597.hp1 HG01192.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.305+3009_305+3010i others(12): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470966 | ||||||
| chr13:49470968 | T | TTCTTTCT others(3): Show |
2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG01928.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.305+3009_305+3010i others(12): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49470968 | ||||||
| chr13:49471145 | A | AT | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(140): Show |
151 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.305+3197dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471145 | ||||||
| chr13:49471222 | C | T | 2 | a0001c0002t0003g0260 a0001c0002t0003g0261 |
2 | HG02080.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.305+3262C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471222 | |||||||
| chr13:49471276 | C | T | 1 | a0003c0004t0031g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.305+3316C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471276 | |||||||
| chr13:49471285 | A | G | 27 | a0003c0004t0005g0006 a0003c0004t0005g0200 a0003c0004t0005g0201 others(24): Show |
29 | HG01109.hp2 HG01257.hp2 HG02015.hp1 others(26): Show |
intron_variant | MODIFIER | c.305+3325A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471285 | |||||||
| chr13:49471350 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.305+3390A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471350 | |||||||
| chr13:49471411 | C | T | 16 | a0001c0001t0007g0003 a0001c0001t0007g0064 a0001c0001t0007g0078 others(13): Show |
18 | HG01074.hp1 HG01106.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.305+3451C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471411 | |||||||
| chr13:49471420 | C | CT | 30 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0055 others(27): Show |
33 | HG00621.hp2 HG00735.hp2 HG01975.hp2 others(30): Show |
intron_variant | MODIFIER | c.305+3477dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471420 | ||||||
| chr13:49471420 | C | CTT | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.305+3476_305+3477d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471420 | ||||||
| chr13:49471420 | CT | C | 69 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0051 others(66): Show |
79 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.305+3477delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471420 | ||||||
| chr13:49471613 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
173 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.305+3653C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471613 | |||||||
| chr13:49471828 | AG | A | 14 | a0001c0002t0008g0243 a0001c0002t0008g0269 a0001c0002t0008g0270 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.305+3869delG | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471828 | |||||||
| chr13:49471864 | C | G | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.305+3904C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471864 | |||||||
| chr13:49471913 | C | CAT | 3 | a0001c0001t0013g0190 a0001c0014t0003g0264 a0002c0003t0008g0287 |
3 | HG00597.hp1 HG01884.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.305+3974_305+3975d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | ||||||
| chr13:49471913 | C | CATATAT | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(3): Show |
6 | HG01346.hp1 HG02004.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.305+3970_305+3975d others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | ||||||
| chr13:49471913 | C | CATATATA others(1): Show |
3 | a0001c0001t0023g0120 a0001c0002t0007g0011 a0001c0002t0029g0228 |
4 | HG01257.hp1 HG01258.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+3968_305+3975d others(10): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | ||||||
| chr13:49471913 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.305+3966_305+3975d others(12): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | ||||||
| chr13:49471913 | C | CATATATA others(5): Show |
29 | a0001c0002t0004g0331 a0001c0002t0004g0335 a0001c0002t0004g0337 others(26): Show |
30 | HG00642.hp1 HG02132.hp1 HG02155.hp1 others(27): Show |
intron_variant | MODIFIER | c.305+3964_305+3975d others(14): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | ||||||
| chr13:49471913 | C | CATATATA others(7): Show |
4 | a0001c0002t0004g0220 a0001c0002t0004g0353 a0001c0002t0004g0361 others(1): Show |
4 | HG00408.hp2 HG02135.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.305+3962_305+3975d others(16): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | ||||||
| chr13:49471913 | C | CATATATA others(9): Show |
2 | a0001c0002t0009g0373 a0003c0004t0018g0196 |
2 | HG00558.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.305+3960_305+3975d others(18): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | ||||||
| chr13:49471913 | C | CATATATA others(11): Show |
2 | a0001c0002t0004g0342 a0001c0002t0004g0375 |
2 | HG02015.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.305+3958_305+3975d others(20): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | ||||||
| chr13:49471913 | C | CATATATA others(13): Show |
2 | a0001c0002t0004g0340 a0001c0002t0004g0356 |
2 | HG03688.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.305+3956_305+3975d others(22): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471913 | ||||||
| chr13:49471926 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.305+3966A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471926 | |||||||
| chr13:49471927 | TATATATA | T | 9 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.305+3968_305+3974d others(9): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471927 | |||||||
| chr13:49471929 | TA | T | 3 | a0001c0002t0019g0227 a0001c0002t0019g0267 a0001c0002t0019g0275 |
3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.305+3970delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471929 | |||||||
| chr13:49471930 | A | AT | 5 | a0001c0001t0010g0054 a0001c0001t0010g0160 a0001c0001t0010g0170 others(2): Show |
5 | HG01975.hp2 HG02258.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.305+3971dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471930 | ||||||
| chr13:49471930 | A | T | 2 | a0001c0001t0010g0159 a0001c0001t0010g0193 |
2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.305+3970A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471930 | |||||||
| chr13:49471931 | TA | T | 7 | a0001c0002t0008g0269 a0001c0002t0008g0270 a0001c0002t0008g0276 others(4): Show |
7 | HG00639.hp1 HG00738.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.305+3972delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471931 | |||||||
| chr13:49471932 | A | AT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(6): Show |
9 | HG00621.hp2 HG02165.hp2 HG03490.hp2 others(6): Show |
intron_variant | MODIFIER | c.305+3973dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471932 | ||||||
| chr13:49471932 | A | ATTT | 3 | a0003c0004t0005g0203 a0003c0004t0005g0215 a0003c0004t0005g0231 |
3 | HG01257.hp2 HG02015.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.305+3973_305+3974i others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471932 | ||||||
| chr13:49471932 | A | T | 10 | a0001c0001t0010g0054 a0001c0001t0010g0159 a0001c0001t0010g0160 others(7): Show |
10 | HG01975.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.305+3972A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471932 | |||||||
| chr13:49471933 | TA | T | 6 | a0001c0002t0008g0243 a0001c0002t0008g0273 a0001c0002t0008g0274 others(3): Show |
6 | HG00741.hp1 HG01106.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.305+3974delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471933 | |||||||
| chr13:49471934 | A | AT | 7 | a0001c0001t0001g0166 a0001c0001t0021g0059 a0001c0002t0003g0229 others(4): Show |
7 | HG01192.hp2 HG02080.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.305+3989dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | ||||||
| chr13:49471934 | A | ATATATAT others(4): Show |
1 | a0001c0002t0004g0346 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.305+3975_305+3976i others(13): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | ||||||
| chr13:49471934 | A | ATATATAT others(6): Show |
1 | a0001c0002t0004g0355 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.305+3975_305+3976i others(15): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | ||||||
| chr13:49471934 | A | ATATATAT others(5): Show |
3 | a0001c0002t0004g0330 a0001c0002t0004g0334 a0001c0002t0024g0371 |
3 | HG02027.hp1 HG02602.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.305+3975_305+3976i others(14): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | ||||||
| chr13:49471934 | A | ATATATAT others(4): Show |
1 | a0001c0002t0004g0358 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.305+3975_305+3976i others(13): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | ||||||
| chr13:49471934 | A | ATATT | 8 | a0001c0001t0001g0157 a0003c0004t0005g0204 a0003c0004t0005g0205 others(5): Show |
8 | HG02109.hp2 HG02132.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | ||||||
| chr13:49471934 | A | ATTTT | 12 | a0003c0004t0005g0006 a0003c0004t0005g0200 a0003c0004t0005g0201 others(9): Show |
12 | HG01109.hp2 HG02083.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.305+3986_305+3989d others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | ||||||
| chr13:49471934 | A | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(33): Show |
36 | HG00621.hp2 HG00639.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.305+3974A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471934 | |||||||
| chr13:49471934 | AT | A | 5 | a0001c0002t0004g0015 a0001c0002t0004g0265 a0001c0002t0004g0266 others(2): Show |
7 | HG01070.hp1 HG01071.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.305+3989delT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49471934 | ||||||
| chr13:49471935 | T | TA | 39 | a0001c0001t0005g0333 a0001c0001t0013g0060 a0001c0001t0013g0063 others(36): Show |
47 | HG00408.hp1 HG00642.hp2 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(3): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | |||||||
| chr13:49471935 | T | TATA | 26 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0026 others(23): Show |
28 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | |||||||
| chr13:49471935 | T | TATATA | 59 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(56): Show |
64 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | |||||||
| chr13:49471935 | T | TATATATA | 22 | a0001c0001t0001g0042 a0001c0001t0001g0049 a0001c0001t0001g0086 others(19): Show |
22 | HG00609.hp1 HG01099.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(9): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | |||||||
| chr13:49471935 | T | TATATATA others(2): Show |
12 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0096 others(9): Show |
12 | HG00621.hp1 HG01358.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(11): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | |||||||
| chr13:49471935 | T | TATATATA others(4): Show |
7 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0122 others(4): Show |
7 | HG03704.hp2 HG04204.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.305+3975_305+3976i others(13): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | |||||||
| chr13:49471935 | T | TATATATA others(6): Show |
2 | a0001c0001t0001g0109 a0001c0002t0026g0329 |
2 | HG02886.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.305+3975_305+3976i others(15): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | |||||||
| chr13:49471935 | T | TATATATA others(10): Show |
1 | a0003c0004t0020g0194 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.305+3975_305+3976i others(19): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | |||||||
| chr13:49471935 | T | TATATATA others(12): Show |
2 | a0003c0004t0018g0197 a0007c0009t0020g0195 |
2 | HG01109.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.305+3975_305+3976i others(21): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471935 | |||||||
| chr13:49471936 | T | A | 26 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(23): Show |
28 | HG00597.hp1 HG00642.hp1 HG01346.hp1 others(25): Show |
intron_variant | MODIFIER | c.305+3976T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471936 | |||||||
| chr13:49471937 | T | A | 111 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(108): Show |
117 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.305+3977T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471937 | |||||||
| chr13:49471938 | T | A | 15 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(12): Show |
17 | HG01346.hp1 HG02004.hp1 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.305+3978T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471938 | |||||||
| chr13:49471939 | T | A | 50 | a0001c0001t0001g0010 a0001c0001t0001g0031 a0001c0001t0001g0042 others(47): Show |
52 | HG00438.hp1 HG00639.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.305+3979T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471939 | |||||||
| chr13:49471940 | T | A | 6 | a0001c0001t0001g0088 a0001c0001t0001g0106 a0001c0001t0001g0187 others(3): Show |
6 | HG02004.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.305+3980T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471940 | |||||||
| chr13:49471941 | T | A | 15 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0101 others(12): Show |
15 | HG01168.hp1 HG02055.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.305+3981T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471941 | |||||||
| chr13:49471942 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.305+3982T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49471942 | |||||||
| chr13:49472108 | A | G | 1 | a0001c0002t0011g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.305+4148A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49472108 | |||||||
| chr13:49472526 | T | C | 1 | a0001c0002t0012g0281 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.306-3950T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49472526 | |||||||
| chr13:49472621 | C | A | 1 | a0002c0003t0002g0296 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.306-3855C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49472621 | |||||||
| chr13:49473301 | G | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(17): Show |
22 | HG00621.hp2 HG01975.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.306-3175G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473301 | |||||||
| chr13:49473393 | A | T | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.306-3083A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473393 | |||||||
| chr13:49473419 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 |
3 | HG01346.hp1 HG02004.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.306-3057C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473419 | |||||||
| chr13:49473444 | G | A | 1 | a0001c0001t0023g0133 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.306-3032G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473444 | |||||||
| chr13:49473485 | A | G | 8 | a0001c0001t0007g0003 a0001c0001t0007g0064 a0001c0001t0007g0078 others(5): Show |
10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.306-2991A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473485 | |||||||
| chr13:49473497 | A | G | 1 | a0001c0002t0004g0361 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.306-2979A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473497 | |||||||
| chr13:49473505 | T | G | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.306-2971T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473505 | |||||||
| chr13:49473551 | C | CA | 45 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0034 others(42): Show |
48 | HG00741.hp2 HG01192.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.306-2903dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49473551 | ||||||
| chr13:49473551 | C | CAA | 64 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(61): Show |
72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.306-2904_306-2903d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49473551 | ||||||
| chr13:49473551 | C | CAAA | 22 | a0001c0002t0003g0237 a0001c0002t0003g0256 a0001c0002t0003g0260 others(19): Show |
22 | HG00642.hp1 HG01952.hp1 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.306-2905_306-2903d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49473551 | ||||||
| chr13:49473551 | CA | C | 8 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0094 others(5): Show |
8 | HG00140.hp1 HG01074.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.306-2903delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49473551 | ||||||
| chr13:49473845 | G | A | 3 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0008t0005g0009 |
4 | HG02717.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.306-2631G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473845 | |||||||
| chr13:49473852 | G | C | 1 | a0001c0002t0008g0243 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.306-2624G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49473852 | |||||||
| chr13:49474019 | T | C | 1 | a0003c0004t0005g0205 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.306-2457T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474019 | |||||||
| chr13:49474265 | C | CA | 84 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(81): Show |
95 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.306-2201dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49474265 | ||||||
| chr13:49474354 | T | G | 1 | a0001c0001t0001g0097 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.306-2122T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474354 | |||||||
| chr13:49474363 | G | T | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.306-2113G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474363 | |||||||
| chr13:49474444 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(17): Show |
22 | HG00621.hp2 HG01975.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.306-2032C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474444 | |||||||
| chr13:49474521 | T | A | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.306-1955T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474521 | |||||||
| chr13:49474614 | G | A | 4 | a0004c0005t0006g0066 a0004c0005t0006g0067 a0004c0005t0006g0068 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.306-1862G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474614 | |||||||
| chr13:49474698 | G | A | 1 | a0001c0001t0042g0144 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.306-1778G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474698 | |||||||
| chr13:49474734 | G | C | 2 | a0001c0002t0007g0011 a0001c0002t0029g0228 |
3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.306-1742G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474734 | |||||||
| chr13:49474839 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
172 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.306-1637A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474839 | |||||||
| chr13:49474839 | A | T | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.306-1637A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49474839 | |||||||
| chr13:49475005 | C | T | 3 | a0001c0002t0019g0227 a0001c0002t0019g0267 a0001c0002t0019g0275 |
3 | HG02572.hp2 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.306-1471C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475005 | |||||||
| chr13:49475014 | G | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.306-1462G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475014 | |||||||
| chr13:49475241 | G | T | 7 | a0001c0001t0001g0010 a0001c0001t0001g0057 a0001c0001t0001g0172 others(4): Show |
8 | HG00639.hp2 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.306-1235G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475241 | |||||||
| chr13:49475491 | A | AT | 8 | a0001c0001t0001g0109 a0001c0001t0027g0189 a0001c0002t0003g0230 others(5): Show |
8 | HG01109.hp1 HG01192.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.306-972dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr13 | 49475491 | ||||||
| chr13:49475608 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.306-868C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475608 | |||||||
| chr13:49475651 | T | C | 14 | a0001c0002t0008g0243 a0001c0002t0008g0269 a0001c0002t0008g0270 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.306-825T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475651 | |||||||
| chr13:49475716 | G | A | 1 | a0002c0003t0002g0297 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.306-760G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475716 | |||||||
| chr13:49475747 | C | T | 1 | a0001c0002t0009g0021 | 2 | NA19064.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.306-729C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475747 | |||||||
| chr13:49475800 | T | A | 4 | a0001c0002t0004g0375 a0001c0002t0019g0227 a0001c0002t0019g0267 others(1): Show |
4 | HG02015.hp2 HG02572.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.306-676T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49475800 | |||||||
| chr13:49476184 | G | T | 2 | a0001c0002t0007g0011 a0001c0002t0029g0228 |
3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.306-292G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49476184 | |||||||
| chr13:49476232 | G | A | 3 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0008t0005g0009 |
4 | HG02717.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.306-244G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49476232 | |||||||
| chr13:49476259 | T | C | 1 | a0001c0002t0029g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.306-217T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 5/13 | chr13 | 49476259 | |||||||
| chr13:49477059 | G | A | 2 | a0002c0003t0002g0318 a0002c0003t0002g0319 |
2 | NA18984.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.869+20G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477059 | |||||||
| chr13:49477089 | G | A | 1 | a0001c0002t0029g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.869+50G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477089 | |||||||
| chr13:49477201 | C | T | 1 | a0004c0005t0006g0072 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.869+162C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477201 | |||||||
| chr13:49477508 | A | C | 1 | a0001c0002t0030g0368 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.869+469A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477508 | |||||||
| chr13:49477529 | A | G | 8 | a0001c0001t0007g0003 a0001c0001t0007g0064 a0001c0001t0007g0078 others(5): Show |
10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.869+490A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477529 | |||||||
| chr13:49477561 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.869+522A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477561 | |||||||
| chr13:49477866 | A | C | 1 | a0001c0001t0001g0040 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.869+827A>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49477866 | |||||||
| chr13:49478016 | T | C | 2 | a0002c0003t0002g0318 a0002c0003t0002g0319 |
2 | NA18984.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.869+977T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478016 | |||||||
| chr13:49478157 | T | C | 2 | a0003c0004t0005g0200 a0003c0004t0005g0201 |
2 | HG02602.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.869+1118T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478157 | |||||||
| chr13:49478319 | A | G | 62 | a0001c0002t0004g0220 a0001c0002t0004g0330 a0001c0002t0004g0331 others(59): Show |
63 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.869+1280A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478319 | |||||||
| chr13:49478363 | G | A | 1 | a0001c0002t0003g0253 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.869+1324G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478363 | |||||||
| chr13:49478523 | A | G | 1 | a0001c0002t0004g0342 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.869+1484A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478523 | |||||||
| chr13:49478548 | C | T | 1 | a0001c0002t0011g0272 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.869+1509C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478548 | |||||||
| chr13:49478927 | A | G | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
346 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.870-1292A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478927 | |||||||
| chr13:49478992 | G | A | 1 | a0001c0001t0041g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.870-1227G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49478992 | |||||||
| chr13:49479051 | A | G | 1 | a0001c0002t0011g0268 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.870-1168A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49479051 | |||||||
| chr13:49479227 | ATG | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
173 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.870-989_870-988del others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr13 | 49479227 | ||||||
| chr13:49479499 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.870-720A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49479499 | |||||||
| chr13:49479582 | G | A | 3 | a0001c0002t0012g0016 a0001c0002t0012g0280 a0001c0002t0012g0281 |
4 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.870-637G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49479582 | |||||||
| chr13:49479599 | C | T | 1 | a0002c0003t0008g0287 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.870-620C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49479599 | |||||||
| chr13:49479740 | G | A | 8 | a0001c0001t0007g0003 a0001c0001t0007g0064 a0001c0001t0007g0078 others(5): Show |
10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.870-479G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49479740 | |||||||
| chr13:49480017 | A | G | 1 | a0001c0010t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.870-202A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49480017 | |||||||
| chr13:49480050 | T | C | 1 | a0004c0005t0006g0066 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.870-169T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49480050 | |||||||
| chr13:49480172 | G | A | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
346 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.870-47G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49480172 | |||||||
| chr13:49480210 | G | T | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
346 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.870-9G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 6/13 | chr13 | 49480210 | |||||||
| chr13:49480575 | C | T | 4 | a0001c0002t0012g0016 a0001c0002t0012g0280 a0001c0002t0012g0281 others(1): Show |
5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.986+240C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 7/13 | chr13 | 49480575 | |||||||
| chr13:49480611 | G | A | 1 | a0001c0001t0028g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.986+276G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 7/13 | chr13 | 49480611 | |||||||
| chr13:49480658 | A | G | 3 | a0001c0002t0004g0015 a0001c0002t0004g0265 a0001c0002t0004g0266 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.987-289A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 7/13 | chr13 | 49480658 | |||||||
| chr13:49480702 | A | G | 1 | a0001c0001t0027g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.987-245A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 7/13 | chr13 | 49480702 | |||||||
| chr13:49480823 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.987-124G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 7/13 | chr13 | 49480823 | |||||||
| chr13:49481296 | G | A | 1 | a0001c0001t0028g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1156+180G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481296 | |||||||
| chr13:49481436 | T | TA | 15 | a0001c0002t0004g0353 a0001c0002t0004g0355 a0002c0003t0002g0018 others(12): Show |
16 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1156+331dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr13 | 49481436 | ||||||
| chr13:49481437 | A | G | 2 | a0001c0002t0007g0011 a0001c0002t0029g0228 |
3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1156+321A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481437 | |||||||
| chr13:49481547 | T | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0091 a0001c0001t0001g0101 others(4): Show |
7 | HG00733.hp1 HG01168.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156+431T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481547 | |||||||
| chr13:49481748 | A | G | 4 | a0001c0002t0012g0016 a0001c0002t0012g0280 a0001c0002t0012g0281 others(1): Show |
5 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1156+632A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481748 | |||||||
| chr13:49481837 | A | AG | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1156+721_1156+722i others(3): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481837 | |||||||
| chr13:49481864 | G | T | 8 | a0001c0002t0003g0001 a0001c0002t0003g0233 a0001c0002t0003g0240 others(5): Show |
12 | NA18612.hp1 NA18953.hp2 NA18967.hp1 others(9): Show |
intron_variant | MODIFIER | c.1156+748G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49481864 | |||||||
| chr13:49482001 | G | A | 8 | a0001c0001t0013g0060 a0001c0001t0013g0061 a0001c0001t0013g0063 others(5): Show |
8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157-736G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49482001 | |||||||
| chr13:49482149 | G | A | 1 | a0002c0003t0015g0317 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1157-588G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49482149 | |||||||
| chr13:49482265 | G | A | 5 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1157-472G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49482265 | |||||||
| chr13:49482265 | G | C | 1 | a0001c0001t0001g0163 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1157-472G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49482265 | |||||||
| chr13:49482657 | T | C | 33 | a0003c0004t0005g0006 a0003c0004t0005g0200 a0003c0004t0005g0201 others(30): Show |
35 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.1157-80T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 8/13 | chr13 | 49482657 | |||||||
| chr13:49483015 | G | T | 6 | a0001c0001t0007g0079 a0001c0001t0007g0081 a0001c0002t0012g0016 others(3): Show |
7 | HG02818.hp1 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1382+53G>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483015 | |||||||
| chr13:49483151 | A | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(118): Show |
126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1382+189A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483151 | |||||||
| chr13:49483210 | T | C | 8 | a0001c0001t0013g0060 a0001c0001t0013g0061 a0001c0001t0013g0063 others(5): Show |
8 | HG01074.hp1 HG01243.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1382+248T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483210 | |||||||
| chr13:49483269 | T | C | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1383-195T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483269 | |||||||
| chr13:49483276 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1383-188A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483276 | |||||||
| chr13:49483380 | G | A | 1 | a0005c0006t0003g0236 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1383-84G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 9/13 | chr13 | 49483380 | |||||||
| chr13:49483609 | A | AT | 22 | a0002c0003t0002g0007 a0002c0003t0002g0285 a0002c0003t0002g0297 others(19): Show |
25 | HG00140.hp2 HG00609.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1482+83dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | ||||||
| chr13:49483609 | A | ATT | 13 | a0002c0003t0002g0085 a0002c0003t0002g0284 a0002c0003t0002g0294 others(10): Show |
13 | HG01123.hp1 HG01934.hp1 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.1482+82_1482+83dup others(2): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | ||||||
| chr13:49483609 | ATTTTTT | A | 8 | a0001c0002t0004g0356 a0001c0002t0026g0329 a0003c0004t0005g0205 others(5): Show |
8 | HG02145.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1482+78_1482+83del others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | ||||||
| chr13:49483609 | ATTTTTTT | A | 57 | a0001c0001t0001g0026 a0001c0001t0001g0042 a0001c0001t0001g0043 others(54): Show |
59 | HG00408.hp2 HG00733.hp1 HG01069.hp2 others(56): Show |
intron_variant | MODIFIER | c.1482+77_1482+83del others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | ||||||
| chr13:49483609 | ATTTTTTT others(1): Show |
A | 129 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(126): Show |
135 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1482+76_1482+83del others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | ||||||
| chr13:49483609 | ATTTTTTT others(2): Show |
A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0031 others(59): Show |
67 | HG00280.hp2 HG00735.hp2 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.1482+75_1482+83del others(9): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | ||||||
| chr13:49483609 | ATTTTTTT others(3): Show |
A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0055 others(41): Show |
53 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1482+74_1482+83del others(10): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | ||||||
| chr13:49483609 | ATTTTTTT others(4): Show |
A | 19 | a0001c0001t0001g0157 a0001c0001t0001g0162 a0001c0001t0007g0164 others(16): Show |
19 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1482+73_1482+83del others(11): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | ||||||
| chr13:49483609 | ATTTTTTT others(10): Show |
A | 3 | a0001c0002t0012g0016 a0001c0002t0012g0280 a0001c0002t0012g0281 |
4 | HG02818.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1482+67_1482+83del others(17): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | ||||||
| chr13:49483609 | ATTTTTTT others(11): Show |
A | 1 | a0001c0002t0012g0282 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1482+66_1482+83del others(18): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483609 | ||||||
| chr13:49483728 | G | A | 1 | a0002c0003t0002g0324 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1482+165G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49483728 | |||||||
| chr13:49483800 | A | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
173 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.1482+237A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49483800 | |||||||
| chr13:49483860 | C | T | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1482+297C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49483860 | |||||||
| chr13:49483974 | AAATGTTT others(10): Show |
A | 63 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(60): Show |
72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1482+413_1482+429d others(19): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr13 | 49483974 | ||||||
| chr13:49484034 | G | A | 1 | a0001c0010t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1482+471G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484034 | |||||||
| chr13:49484266 | T | G | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1482+703T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484266 | |||||||
| chr13:49484409 | A | G | 2 | a0001c0002t0007g0011 a0001c0002t0029g0228 |
3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1482+846A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484409 | |||||||
| chr13:49484422 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1482+859A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484422 | |||||||
| chr13:49484530 | G | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1482+967G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484530 | |||||||
| chr13:49484549 | C | T | 2 | a0001c0002t0007g0011 a0001c0002t0029g0228 |
3 | HG01257.hp1 HG01258.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1482+986C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484549 | |||||||
| chr13:49484550 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(122): Show |
131 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1482+987G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484550 | |||||||
| chr13:49484696 | T | G | 1 | a0001c0001t0001g0037 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1483-934T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484696 | |||||||
| chr13:49484702 | G | A | 15 | a0001c0002t0007g0011 a0001c0002t0029g0228 a0003c0004t0005g0202 others(12): Show |
16 | HG01109.hp2 HG01257.hp1 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1483-928G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484702 | |||||||
| chr13:49484731 | A | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1483-899A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484731 | |||||||
| chr13:49484942 | T | C | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1483-688T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49484942 | |||||||
| chr13:49485218 | C | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1483-412C>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49485218 | |||||||
| chr13:49485395 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(118): Show |
126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1483-235T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49485395 | |||||||
| chr13:49485520 | C | T | 2 | a0001c0002t0008g0273 a0001c0002t0008g0274 |
2 | HG00741.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1483-110C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49485520 | |||||||
| chr13:49485535 | T | C | 14 | a0003c0004t0005g0006 a0003c0004t0005g0200 a0003c0004t0005g0201 others(11): Show |
16 | HG01257.hp2 HG02015.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1483-95T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 10/13 | chr13 | 49485535 | |||||||
| chr13:49485788 | C | G | 1 | a0003c0004t0031g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1576+65C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49485788 | |||||||
| chr13:49486030 | TA | T | 14 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0066 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1576+310delA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr13 | 49486030 | ||||||
| chr13:49486033 | A | G | 1 | a0001c0002t0029g0228 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1576+310A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486033 | |||||||
| chr13:49486063 | G | A | 1 | a0001c0002t0003g0246 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1576+340G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486063 | |||||||
| chr13:49486281 | G | A | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(1): Show |
4 | HG00438.hp2 NA18960.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1576+558G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486281 | |||||||
| chr13:49486303 | C | CA | 38 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(35): Show |
42 | HG00621.hp2 HG01074.hp1 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.1576+591dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr13 | 49486303 | ||||||
| chr13:49486303 | C | CAA | 125 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(122): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1576+590_1576+591d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr13 | 49486303 | ||||||
| chr13:49486303 | C | CAAA | 71 | a0001c0001t0007g0003 a0001c0001t0007g0064 a0001c0001t0007g0078 others(68): Show |
82 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.1576+589_1576+591d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr13 | 49486303 | ||||||
| chr13:49486310 | A | AAT | 56 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0041 others(53): Show |
58 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1576+588_1576+589i others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr13 | 49486310 | ||||||
| chr13:49486310 | A | T | 1 | a0003c0004t0031g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1576+587A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486310 | |||||||
| chr13:49486333 | G | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1576+610G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486333 | |||||||
| chr13:49486402 | G | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0033 |
2 | HG00735.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1576+679G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486402 | |||||||
| chr13:49486510 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1576+787A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486510 | |||||||
| chr13:49486540 | T | G | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
346 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.1576+817T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486540 | |||||||
| chr13:49486568 | T | C | 1 | a0002c0003t0002g0309 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1576+845T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486568 | |||||||
| chr13:49486613 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1576+890G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486613 | |||||||
| chr13:49486666 | C | T | 1 | a0003c0004t0018g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1576+943C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486666 | |||||||
| chr13:49486674 | A | G | 1 | a0001c0002t0026g0329 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1576+951A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486674 | |||||||
| chr13:49486842 | G | A | 1 | a0001c0002t0003g0258 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1576+1119G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486842 | |||||||
| chr13:49486984 | T | C | 3 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0008t0005g0009 |
4 | HG02717.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1576+1261T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49486984 | |||||||
| chr13:49487075 | G | A | 4 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0008g0273 others(1): Show |
4 | HG00741.hp1 HG01993.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1577-1215G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487075 | |||||||
| chr13:49487136 | G | A | 1 | a0001c0002t0022g0336 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1577-1154G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487136 | |||||||
| chr13:49487376 | C | T | 1 | a0001c0001t0007g0164 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1577-914C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487376 | |||||||
| chr13:49487514 | A | T | 291 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1577-776A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487514 | |||||||
| chr13:49487675 | T | A | 2 | a0001c0002t0004g0330 a0001c0002t0004g0334 |
2 | HG02027.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1577-615T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487675 | |||||||
| chr13:49487706 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1577-584C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487706 | |||||||
| chr13:49487709 | T | C | 9 | a0001c0001t0007g0003 a0001c0001t0007g0064 a0001c0001t0007g0078 others(6): Show |
11 | HG01106.hp1 HG01884.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1577-581T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487709 | |||||||
| chr13:49487974 | T | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1577-316T>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49487974 | |||||||
| chr13:49488037 | G | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(287): Show |
311 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.1577-253G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49488037 | |||||||
| chr13:49488191 | C | T | 323 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(320): Show |
346 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(343): Show |
intron_variant | MODIFIER | c.1577-99C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49488191 | |||||||
| chr13:49488222 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1577-68G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 11/13 | chr13 | 49488222 | |||||||
| chr13:49488686 | T | G | 1 | a0001c0001t0013g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1917+56T>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49488686 | |||||||
| chr13:49488775 | T | C | 14 | a0001c0002t0008g0243 a0001c0002t0008g0269 a0001c0002t0008g0270 others(11): Show |
14 | HG00639.hp1 HG00738.hp1 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1917+145T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49488775 | |||||||
| chr13:49488812 | A | G | 63 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(60): Show |
72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1917+182A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49488812 | |||||||
| chr13:49488823 | A | T | 48 | a0001c0002t0004g0220 a0001c0002t0004g0330 a0001c0002t0004g0331 others(45): Show |
49 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.1917+193A>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49488823 | |||||||
| chr13:49488831 | C | T | 3 | a0001c0002t0004g0015 a0001c0002t0004g0265 a0001c0002t0004g0266 |
4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1917+201C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49488831 | |||||||
| chr13:49489102 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
173 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.1917+472C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489102 | |||||||
| chr13:49489165 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1917+535A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489165 | |||||||
| chr13:49489189 | C | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(100): Show |
107 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1917+559C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489189 | |||||||
| chr13:49489224 | C | T | 63 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(60): Show |
72 | HG00408.hp1 HG00597.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1917+594C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489224 | |||||||
| chr13:49489318 | C | G | 4 | a0001c0002t0004g0341 a0001c0002t0004g0348 a0001c0002t0004g0350 others(1): Show |
4 | NA18942.hp1 NA18943.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.1917+688C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489318 | |||||||
| chr13:49489375 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(286): Show |
310 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.1917+745G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489375 | |||||||
| chr13:49489497 | T | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(17): Show |
22 | HG00621.hp2 HG01975.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1917+867T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489497 | |||||||
| chr13:49489502 | T | TA | 29 | a0001c0001t0001g0057 a0001c0001t0001g0115 a0001c0001t0010g0054 others(26): Show |
33 | HG00408.hp1 HG01884.hp2 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.1917+888dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489502 | ||||||
| chr13:49489512 | A | G | 4 | a0004c0005t0006g0066 a0004c0005t0006g0067 a0004c0005t0006g0068 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1917+882A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489512 | |||||||
| chr13:49489551 | C | G | 291 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(288): Show |
312 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(309): Show |
intron_variant | MODIFIER | c.1917+921C>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489551 | |||||||
| chr13:49489596 | C | CT | 36 | a0001c0001t0001g0101 a0001c0001t0001g0113 a0001c0001t0001g0141 others(33): Show |
38 | HG01069.hp2 HG01109.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1917+985dupT | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489596 | ||||||
| chr13:49489596 | C | CTT | 210 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(207): Show |
230 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.1917+984_1917+985d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489596 | ||||||
| chr13:49489596 | C | CTTT | 77 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0086 others(74): Show |
78 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.1917+983_1917+985d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489596 | ||||||
| chr13:49489621 | C | T | 46 | a0001c0002t0004g0220 a0001c0002t0004g0330 a0001c0002t0004g0331 others(43): Show |
47 | HG00408.hp2 HG00558.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1917+991C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489621 | |||||||
| chr13:49489643 | C | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG00609.hp1 HG01255.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.1917+1013C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489643 | |||||||
| chr13:49489665 | C | T | 70 | a0001c0002t0004g0220 a0001c0002t0004g0330 a0001c0002t0004g0331 others(67): Show |
73 | HG00280.hp1 HG00408.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1917+1035C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489665 | |||||||
| chr13:49489675 | C | T | 1 | a0001c0008t0005g0009 | 2 | HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1917+1045C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489675 | |||||||
| chr13:49489714 | G | C | 10 | a0004c0005t0006g0024 a0004c0005t0006g0065 a0004c0005t0006g0070 others(7): Show |
10 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1917+1084G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489714 | |||||||
| chr13:49489738 | G | A | 171 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
180 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.1918-1084G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489738 | |||||||
| chr13:49489769 | C | T | 1 | a0001c0002t0003g0258 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1918-1053C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489769 | |||||||
| chr13:49489842 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA18966.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1918-980T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489842 | |||||||
| chr13:49489886 | G | A | 2 | a0001c0001t0041g0117 a0001c0002t0019g0227 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1918-936G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489886 | |||||||
| chr13:49489906 | C | T | 5 | a0003c0004t0018g0196 a0003c0004t0018g0197 a0003c0004t0018g0198 others(2): Show |
5 | HG01109.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1918-916C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489906 | |||||||
| chr13:49489907 | G | GC | 52 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(49): Show |
58 | HG00408.hp2 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.1918-904dupC | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489907 | ||||||
| chr13:49489907 | G | GCC | 17 | a0001c0001t0013g0060 a0001c0001t0013g0063 a0001c0001t0017g0028 others(14): Show |
17 | HG01243.hp2 HG02056.hp2 HG02698.hp1 others(14): Show |
intron_variant | MODIFIER | c.1918-905_1918-904d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489907 | ||||||
| chr13:49489907 | GC | G | 49 | a0001c0002t0003g0001 a0001c0002t0003g0012 a0001c0002t0003g0225 others(46): Show |
57 | HG00408.hp1 HG01081.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.1918-904delC | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49489907 | ||||||
| chr13:49489918 | C | CCCT | 25 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0034 others(22): Show |
26 | HG00280.hp2 HG00735.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.1918-904_1918-903i others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489918 | |||||||
| chr13:49489918 | C | CCT | 33 | a0001c0001t0010g0159 a0002c0003t0002g0019 a0002c0003t0002g0084 others(30): Show |
34 | HG00140.hp2 HG01071.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1918-904_1918-903i others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489918 | |||||||
| chr13:49489918 | C | T | 25 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0095 others(22): Show |
27 | HG00438.hp2 HG00597.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1918-904C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489918 | |||||||
| chr13:49489919 | T | C | 64 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0025 others(61): Show |
67 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.1918-903T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489919 | |||||||
| chr13:49489927 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0031 others(26): Show |
32 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1918-895T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489927 | |||||||
| chr13:49489927 | T | TC | 34 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0048 others(31): Show |
34 | HG00609.hp1 HG00639.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1918-895_1918-894i others(3): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489927 | |||||||
| chr13:49489928 | T | TC | 27 | a0001c0001t0005g0333 a0001c0002t0009g0364 a0001c0002t0009g0366 others(24): Show |
33 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1918-894_1918-893i others(3): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489928 | |||||||
| chr13:49489928 | T | TCC | 63 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0025 others(60): Show |
66 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1918-894_1918-893i others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489928 | |||||||
| chr13:49489949 | T | C | 38 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0001t0007g0064 others(35): Show |
40 | HG01106.hp1 HG01109.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1918-873T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49489949 | |||||||
| chr13:49490095 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1918-727G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490095 | |||||||
| chr13:49490137 | G | A | 35 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0003c0004t0005g0006 others(32): Show |
37 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.1918-685G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490137 | |||||||
| chr13:49490279 | C | CA | 27 | a0001c0002t0003g0248 a0001c0002t0004g0330 a0001c0002t0004g0331 others(24): Show |
28 | HG00408.hp2 HG00735.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1918-520dupA | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | ||||||
| chr13:49490279 | C | CAA | 59 | a0001c0001t0001g0005 a0001c0001t0001g0056 a0001c0001t0001g0157 others(56): Show |
69 | HG00408.hp1 HG00597.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1918-521_1918-520d others(4): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | ||||||
| chr13:49490279 | C | CAAA | 39 | a0001c0001t0001g0055 a0001c0001t0001g0086 a0001c0001t0001g0097 others(36): Show |
41 | HG00621.hp2 HG01074.hp1 HG01074.hp2 others(38): Show |
intron_variant | MODIFIER | c.1918-522_1918-520d others(5): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | ||||||
| chr13:49490279 | C | CAAAA | 85 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0010 others(82): Show |
91 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.1918-523_1918-520d others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | ||||||
| chr13:49490279 | C | CAAAAA | 47 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0036 others(44): Show |
47 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1918-524_1918-520d others(7): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | ||||||
| chr13:49490279 | C | CAAAAAA | 10 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0096 others(7): Show |
11 | HG00558.hp1 HG00741.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.1918-525_1918-520d others(8): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | ||||||
| chr13:49490279 | C | CAAAAAAA others(9): Show |
1 | a0003c0004t0031g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1918-535_1918-520d others(18): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | ||||||
| chr13:49490279 | CAAAA | C | 27 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0003g0229 others(24): Show |
29 | HG01109.hp2 HG01192.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1918-523_1918-520d others(6): Show |
SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr13 | 49490279 | ||||||
| chr13:49490571 | G | A | 2 | a0002c0003t0002g0084 a0002c0003t0002g0085 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1918-251G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490571 | |||||||
| chr13:49490579 | T | C | 1 | a0002c0003t0034g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1918-243T>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490579 | |||||||
| chr13:49490703 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(286): Show |
309 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.1918-119G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490703 | |||||||
| chr13:49490792 | C | T | 2 | a0001c0002t0029g0228 a0002c0003t0034g0306 |
2 | HG02280.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1918-30C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 12/13 | chr13 | 49490792 | |||||||
| chr13:49490926 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(10): Show |
15 | HG00621.hp2 HG02165.hp2 HG03490.hp2 others(12): Show |
intron_variant | MODIFIER | c.2006+16C>T | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49490926 | |||||||
| chr13:49490947 | G | A | 40 | a0001c0001t0005g0332 a0001c0001t0005g0333 a0001c0002t0012g0016 others(37): Show |
44 | HG01109.hp1 HG01109.hp2 HG01257.hp2 others(41): Show |
intron_variant | MODIFIER | c.2006+37G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49490947 | |||||||
| chr13:49491053 | G | C | 1 | a0002c0003t0034g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2006+143G>C | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49491053 | |||||||
| chr13:49491074 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(286): Show |
309 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.2006+164G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49491074 | |||||||
| chr13:49491341 | A | G | 8 | a0001c0001t0007g0003 a0001c0001t0007g0064 a0001c0001t0007g0078 others(5): Show |
10 | HG01106.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.2007-391A>G | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49491341 | |||||||
| chr13:49491522 | G | A | 1 | a0002c0003t0034g0306 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2007-210G>A | SETDB2 | ENSG00000136169.17 | transcript | ENST00000611815.2 | protein_coding | 13/13 | chr13 | 49491522 |