Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54934 |
| ensemblid | ENSG00000139620.13 |
| hgncid | 26024 |
| symbol | KANSL2 |
| name | KAT8 regulatory NSL complex subunit 2 |
| refseq_nuc | NM_017822.4 |
| refseq_prot | NP_060292.3 |
| ensembl_nuc | ENST00000420613.7 |
| ensembl_prot | ENSP00000415436.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 48653211 |
| end | 48682238 |
| strand | - |
| ver | v1.2 |
| region | chr12:48653211-48682238 |
| region5000 | chr12:48648211-48687238 |
| regionname0 | KANSL2_chr12_48653211_48682238 |
| regionname5000 | KANSL2_chr12_48648211_48687238 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 492 | 161 | 30 | 36 | 65 | 9 | 21 | 45 | KANSL2_chr12_48648211_48687238 | KANSL2 | MNRIR others(487): Show |
chr12 | 48648211 | 48687238 |
| a0002 | 1/1 | 492 | 156 | 62 | 26 | 47 | 4 | 15 | 39 | KANSL2_chr12_48648211_48687238 | KANSL2 | MNRIR others(487): Show |
chr12 | 48648211 | 48687238 |
| a0003 | 0/0 | 492 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | MNRIR others(487): Show |
chr12 | 48648211 | 48687238 |
| a0004 | 0/0 | 492 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | MNRIR others(487): Show |
chr12 | 48648211 | 48687238 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 1476 | 130 | 21 | 27 | 64 | 4 | 14 | KANSL2_chr12_48648211_48687238 | KANSL2 | ATGAA others(1471): Show |
chr12 | 48648211 | 48687238 | ||
| a0001c0003 | 0/0 | 1476 | 29 | 9 | 8 | 0 | 5 | 7 | KANSL2_chr12_48648211_48687238 | KANSL2 | ATGAA others(1471): Show |
chr12 | 48648211 | 48687238 | ||
| a0001c0006 | 0/0 | 1476 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ATGAA others(1471): Show |
chr12 | 48648211 | 48687238 | ||
| a0001c0009 | 0/0 | 1476 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ATGAA others(1471): Show |
chr12 | 48648211 | 48687238 | ||
| a0002c0001 | 1/1 | 1476 | 136 | 44 | 25 | 46 | 4 | 15 | KANSL2_chr12_48648211_48687238 | KANSL2 | ATGAA others(1471): Show |
chr12 | 48648211 | 48687238 | ||
| a0002c0004 | 0/0 | 1476 | 19 | 18 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ATGAA others(1471): Show |
chr12 | 48648211 | 48687238 | ||
| a0002c0007 | 0/0 | 1476 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ATGAA others(1471): Show |
chr12 | 48648211 | 48687238 | ||
| a0003c0005 | 0/0 | 1476 | 4 | 0 | 3 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ATGAA others(1471): Show |
chr12 | 48648211 | 48687238 | ||
| a0004c0008 | 0/0 | 1476 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ATGAA others(1471): Show |
chr12 | 48648211 | 48687238 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 2373 | 127 | 18 | 27 | 64 | 4 | 14 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0001c0002t0003 | 0/0 | 2373 | 3 | 3 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0001c0003t0001 | 0/0 | 2373 | 2 | 2 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0001c0003t0002 | 0/0 | 2371 | 25 | 7 | 6 | 0 | 5 | 7 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2366): Show |
chr12 | 48648211 | 48687238 |
| a0001c0003t0005 | 0/0 | 2371 | 2 | 0 | 2 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2366): Show |
chr12 | 48648211 | 48687238 |
| a0001c0006t0001 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0001c0009t0003 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0002c0001t0001 | 1/1 | 2373 | 131 | 39 | 25 | 46 | 4 | 15 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0002c0001t0004 | 0/0 | 2373 | 4 | 4 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0002c0001t0006 | 0/0 | 2373 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0002c0004t0001 | 0/0 | 2373 | 19 | 18 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0002c0007t0001 | 0/0 | 2373 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0003c0005t0001 | 0/0 | 2373 | 4 | 0 | 3 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| a0004c0008t0001 | 0/0 | 2373 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | ACTAG others(2368): Show |
chr12 | 48648211 | 48687238 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0001 | 0/0 | 16 | 3 | 2 | 11 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0003 | 0/0 | 8 | 0 | 4 | 4 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0005 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0026 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0003t0005g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0006t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0001c0009t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0002 | 0/0 | 11 | 1 | 2 | 7 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0004 | 1/0 | 6 | 0 | 3 | 0 | 0 | 2 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0007 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0072 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0002c0007t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0003c0005t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0003c0005t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| a0004c0008t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0001 | t0001 | g0015 | EUR | GBR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00099 | hp2 | a0001 | c0003 | t0002 | g0037 | EUR | GBR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00323 | hp1 | a0001 | c0003 | t0002 | g0038 | EUR | FIN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0214 | EUR | FIN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00544 | hp1 | a0002 | c0001 | t0001 | g0123 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00558 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00597 | hp1 | a0002 | c0001 | t0001 | g0125 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00621 | hp2 | a0002 | c0001 | t0001 | g0093 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00639 | hp2 | a0002 | c0001 | t0001 | g0077 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0178 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00673 | hp1 | a0002 | c0001 | t0001 | g0109 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0181 | EAS | CHS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00733 | hp1 | a0003 | c0005 | t0001 | g0029 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00735 | hp1 | a0003 | c0005 | t0001 | g0029 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00738 | hp1 | a0002 | c0001 | t0001 | g0054 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00738 | hp2 | a0002 | c0001 | t0001 | g0018 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG00741 | hp2 | a0002 | c0001 | t0001 | g0066 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0192 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01099 | hp1 | a0002 | c0001 | t0001 | g0004 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0223 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0210 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01106 | hp2 | a0002 | c0001 | t0001 | g0080 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01109 | hp1 | a0001 | c0009 | t0003 | g0039 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01168 | hp1 | a0002 | c0001 | t0001 | g0076 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01168 | hp2 | a0002 | c0001 | t0001 | g0068 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0215 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01175 | hp2 | a0002 | c0001 | t0001 | g0074 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01243 | hp1 | a0001 | c0003 | t0002 | g0037 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01243 | hp2 | a0002 | c0001 | t0001 | g0017 | AMR | PUR | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01255 | hp1 | a0001 | c0003 | t0002 | g0225 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01255 | hp2 | a0002 | c0001 | t0001 | g0004 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01256 | hp1 | a0002 | c0001 | t0001 | g0065 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0004 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01257 | hp2 | a0001 | c0003 | t0005 | g0227 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01258 | hp1 | a0001 | c0003 | t0005 | g0229 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01261 | hp1 | a0003 | c0005 | t0001 | g0030 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01346 | hp1 | a0002 | c0004 | t0001 | g0041 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01346 | hp2 | a0002 | c0001 | t0001 | g0078 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01358 | hp1 | a0002 | c0001 | t0001 | g0062 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01361 | hp1 | a0002 | c0001 | t0001 | g0138 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01433 | hp1 | a0002 | c0001 | t0001 | g0073 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0231 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0230 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01515 | hp1 | a0001 | c0003 | t0002 | g0226 | EUR | IBS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01515 | hp2 | a0002 | c0001 | t0001 | g0067 | EUR | IBS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0005 | EUR | IBS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01516 | hp2 | a0001 | c0003 | t0002 | g0233 | EUR | IBS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01517 | hp1 | a0002 | c0001 | t0001 | g0070 | EUR | IBS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01517 | hp2 | a0001 | c0003 | t0002 | g0232 | EUR | IBS | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01884 | hp1 | a0002 | c0001 | t0001 | g0106 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01884 | hp2 | a0002 | c0004 | t0001 | g0044 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01891 | hp1 | a0002 | c0001 | t0004 | g0023 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0194 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01952 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0202 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0006 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01993 | hp1 | a0004 | c0008 | t0001 | g0183 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01993 | hp2 | a0002 | c0001 | t0001 | g0022 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02004 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02015 | hp2 | a0001 | c0006 | t0001 | g0145 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0096 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02055 | hp1 | a0002 | c0001 | t0004 | g0117 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02055 | hp2 | a0002 | c0001 | t0001 | g0114 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02056 | hp2 | a0002 | c0001 | t0001 | g0118 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0165 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02257 | hp1 | a0002 | c0001 | t0001 | g0122 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02257 | hp2 | a0002 | c0004 | t0001 | g0142 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02273 | hp1 | a0002 | c0001 | t0001 | g0090 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02280 | hp1 | a0002 | c0001 | t0001 | g0101 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02280 | hp2 | a0002 | c0001 | t0001 | g0069 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02300 | hp1 | a0002 | c0001 | t0001 | g0022 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0071 | AMR | PEL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02451 | hp1 | a0002 | c0004 | t0001 | g0010 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | KHV | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0216 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02572 | hp2 | a0002 | c0001 | t0001 | g0098 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02602 | hp1 | a0002 | c0001 | t0001 | g0089 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0094 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02615 | hp1 | a0002 | c0001 | t0001 | g0061 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0241 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02622 | hp1 | a0002 | c0001 | t0001 | g0016 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02622 | hp2 | a0002 | c0001 | t0001 | g0104 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0136 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02630 | hp2 | a0002 | c0001 | t0001 | g0099 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02647 | hp1 | a0002 | c0001 | t0001 | g0024 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0187 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0171 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02683 | hp2 | a0002 | c0001 | t0001 | g0004 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02717 | hp1 | a0002 | c0001 | t0001 | g0008 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02717 | hp2 | a0001 | c0003 | t0002 | g0239 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02723 | hp1 | a0002 | c0001 | t0001 | g0024 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0040 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0116 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0038 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02809 | hp1 | a0002 | c0004 | t0001 | g0043 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0220 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02818 | hp1 | a0002 | c0004 | t0001 | g0047 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02818 | hp2 | a0001 | c0003 | t0002 | g0240 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02886 | hp1 | a0002 | c0004 | t0001 | g0042 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02886 | hp2 | a0002 | c0001 | t0001 | g0009 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02895 | hp1 | a0002 | c0001 | t0001 | g0009 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02896 | hp1 | a0002 | c0001 | t0001 | g0007 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02897 | hp2 | a0002 | c0001 | t0001 | g0056 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02922 | hp1 | a0001 | c0003 | t0002 | g0238 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02922 | hp2 | a0002 | c0001 | t0001 | g0131 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02965 | hp1 | a0002 | c0004 | t0001 | g0048 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02965 | hp2 | a0002 | c0001 | t0001 | g0055 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02970 | hp1 | a0002 | c0004 | t0001 | g0046 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02970 | hp2 | a0002 | c0004 | t0001 | g0058 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03041 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03098 | hp1 | a0002 | c0001 | t0001 | g0140 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03098 | hp2 | a0002 | c0004 | t0001 | g0143 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0155 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0156 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03139 | hp1 | a0002 | c0004 | t0001 | g0014 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03139 | hp2 | a0002 | c0004 | t0001 | g0010 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03195 | hp2 | a0002 | c0001 | t0001 | g0100 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03209 | hp1 | a0002 | c0001 | t0001 | g0083 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03209 | hp2 | a0002 | c0004 | t0001 | g0010 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03225 | hp1 | a0002 | c0001 | t0001 | g0129 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03225 | hp2 | a0002 | c0001 | t0001 | g0132 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03453 | hp1 | a0002 | c0001 | t0001 | g0097 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0014 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0179 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03486 | hp2 | a0002 | c0001 | t0001 | g0008 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0189 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03491 | hp1 | a0001 | c0003 | t0002 | g0224 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03491 | hp2 | a0002 | c0001 | t0001 | g0051 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03492 | hp1 | a0002 | c0001 | t0001 | g0006 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03516 | hp1 | a0002 | c0001 | t0001 | g0139 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03516 | hp2 | a0002 | c0001 | t0004 | g0119 | AFR | ESN | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0237 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03540 | hp2 | a0002 | c0001 | t0001 | g0002 | AFR | GWD | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03579 | hp1 | a0002 | c0001 | t0001 | g0009 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03579 | hp2 | a0002 | c0001 | t0001 | g0135 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03654 | hp1 | a0002 | c0001 | t0001 | g0020 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03654 | hp2 | a0001 | c0003 | t0002 | g0236 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0198 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03688 | hp1 | a0001 | c0003 | t0002 | g0221 | SAS | STU | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03688 | hp2 | a0002 | c0001 | t0001 | g0075 | SAS | STU | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03704 | hp1 | a0002 | c0001 | t0001 | g0016 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03710 | hp1 | a0001 | c0003 | t0002 | g0222 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0167 | SAS | PJL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03834 | hp1 | a0002 | c0001 | t0001 | g0004 | SAS | BEB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03834 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | BEB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | BEB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0063 | SAS | BEB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03942 | hp1 | a0002 | c0001 | t0001 | g0079 | SAS | BEB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03942 | hp2 | a0001 | c0003 | t0002 | g0228 | SAS | BEB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0234 | SAS | BEB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | BEB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | STU | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG04204 | hp2 | a0002 | c0001 | t0001 | g0115 | SAS | STU | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG04228 | hp1 | a0002 | c0001 | t0001 | g0064 | SAS | STU | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0193 | SAS | STU | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18522 | hp1 | a0002 | c0004 | t0001 | g0059 | AFR | YRI | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18522 | hp2 | a0002 | c0004 | t0001 | g0141 | AFR | YRI | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18747 | hp1 | a0002 | c0001 | t0001 | g0015 | EAS | CHB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0207 | EAS | CHB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18906 | hp1 | a0002 | c0001 | t0001 | g0108 | AFR | YRI | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0170 | AFR | YRI | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18942 | hp2 | a0002 | c0001 | t0001 | g0053 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18944 | hp2 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18947 | hp2 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0052 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18956 | hp1 | a0002 | c0001 | t0001 | g0088 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18960 | hp1 | a0002 | c0001 | t0001 | g0128 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0120 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18967 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0086 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18970 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18971 | hp1 | a0002 | c0007 | t0001 | g0049 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18971 | hp2 | a0002 | c0001 | t0001 | g0020 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18973 | hp1 | a0002 | c0001 | t0001 | g0111 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18974 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18975 | hp1 | a0002 | c0001 | t0001 | g0113 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18977 | hp2 | a0002 | c0001 | t0001 | g0091 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18979 | hp1 | a0002 | c0001 | t0001 | g0102 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18980 | hp2 | a0002 | c0001 | t0001 | g0082 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18986 | hp2 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18990 | hp1 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18993 | hp2 | a0002 | c0001 | t0001 | g0092 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18994 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19009 | hp2 | a0002 | c0001 | t0001 | g0110 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19010 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | LWK | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19043 | hp2 | a0002 | c0001 | t0001 | g0050 | AFR | LWK | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19057 | hp2 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19062 | hp1 | a0002 | c0001 | t0001 | g0007 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19067 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19067 | hp2 | a0002 | c0001 | t0001 | g0105 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19068 | hp2 | a0002 | c0001 | t0001 | g0095 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19074 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19075 | hp2 | a0002 | c0001 | t0001 | g0127 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19079 | hp2 | a0002 | c0001 | t0001 | g0087 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19083 | hp1 | a0002 | c0001 | t0001 | g0019 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19084 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0208 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19085 | hp2 | a0002 | c0001 | t0001 | g0084 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19087 | hp2 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19089 | hp2 | a0002 | c0001 | t0001 | g0124 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19091 | hp1 | a0002 | c0001 | t0001 | g0021 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19240 | hp1 | a0002 | c0001 | t0001 | g0107 | AFR | YRI | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA19240 | hp2 | a0002 | c0001 | t0006 | g0133 | AFR | YRI | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA20129 | hp1 | a0002 | c0001 | t0004 | g0023 | AFR | ASW | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA20129 | hp2 | a0002 | c0001 | t0001 | g0081 | AFR | ASW | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA20752 | hp1 | a0002 | c0001 | t0001 | g0018 | EUR | TSI | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0217 | EUR | TSI | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA20805 | hp1 | a0003 | c0005 | t0001 | g0030 | EUR | TSI | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0212 | EUR | TSI | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0163 | SAS | GIH | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0218 | SAS | GIH | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01123 | hp1 | a0001 | c0003 | t0002 | g0219 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | CLM | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0235 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02486 | hp1 | a0002 | c0004 | t0001 | g0045 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0195 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG02559 | hp2 | a0002 | c0001 | t0001 | g0130 | AFR | ACB | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| HG03471 | hp2 | a0002 | c0001 | t0001 | g0134 | AFR | MSL | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA18955 | hp2 | a0002 | c0001 | t0001 | g0057 | EAS | JPT | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | USA | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA20300 | hp2 | a0002 | c0001 | t0001 | g0017 | AFR | USA | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA21309 | hp1 | a0001 | c0003 | t0001 | g0060 | AFR | LWK | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| NA21309 | hp2 | a0002 | c0001 | t0001 | g0085 | AFR | LWK | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0072 | REF | REF | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| homoSapiens | grch38p0 | a0002 | c0001 | t0001 | g0004 | REF | REF | KANSL2_chr12_48648211_48687238 | KANSL2 | chr12 | 48648211 | 48687238 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48654130 | G | C | 1 | a0004 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.1393C>G | p.Arg465Gly | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 10/10 | 1454/2373 | 1393/1479 | 465/492 | chr12 | 48654130 | |||
| chr12:48654955 | G | T | 3 | a0001 a0003 a0004 |
166 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(163): Show |
missense_variant | MODERATE | c.1333C>A | p.Pro445Thr | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 9/10 | 1394/2373 | 1333/1479 | 445/492 | chr12 | 48654955 | |||
| chr12:48667728 | T | C | 1 | a0003 | 4 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(1): Show |
missense_variant | MODERATE | c.938A>G | p.Asn313Ser | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/10 | 999/2373 | 938/1479 | 313/492 | chr12 | 48667728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48654998 | T | G | 1 | a0001c0009 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1290A>C | p.Ser430Ser | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 9/10 | 1351/2373 | 1290/1479 | 430/492 | chr12 | 48654998 | |||
| chr12:48671944 | T | C | 2 | a0001c0003 a0002c0004 |
48 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(45): Show |
synonymous_variant | LOW | c.564A>G | p.Thr188Thr | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/10 | 625/2373 | 564/1479 | 188/492 | chr12 | 48671944 | |||
| chr12:48681552 | A | C | 1 | a0002c0007 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.81T>G | p.Ser27Ser | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/10 | 142/2373 | 81/1479 | 27/492 | chr12 | 48681552 | |||
| chr12:48681591 | C | T | 1 | a0001c0006 | 1 | HG02015.hp2 | synonymous_variant | LOW | c.42G>A | p.Gly14Gly | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/10 | 103/2373 | 42/1479 | 14/492 | chr12 | 48681591 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48653676 | C | T | 1 | a0001c0003t0005 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*368G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 10/10 | 368 | chr12 | 48653676 | ||||||
| chr12:48653678 | A | G | 1 | a0002c0001t0004 | 4 | HG01891.hp1 HG02055.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*366T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 10/10 | 366 | chr12 | 48653678 | ||||||
| chr12:48653703 | GAC | G | 2 | a0001c0003t0002 a0001c0003t0005 |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*339_*340delGT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 10/10 | 339 | chr12 | 48653703 | ||||||
| chr12:48653888 | G | A | 1 | a0002c0001t0006 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*156C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 10/10 | 156 | chr12 | 48653888 | ||||||
| chr12:48682200 | C | G | 2 | a0001c0003t0002 a0001c0003t0005 |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-23G>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 1/10 | 568 | chr12 | 48682200 | ||||||
| chr12:48682201 | T | G | 2 | a0001c0003t0002 a0001c0003t0005 |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-24A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 1/10 | 569 | chr12 | 48682201 | ||||||
| chr12:48682221 | C | T | 2 | a0001c0002t0003 a0001c0009t0003 |
4 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-44G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 1/10 | 589 | chr12 | 48682221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:48654244 | T | A | 1 | a0002c0001t0001g0052 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1348-69A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 9/9 | chr12 | 48654244 | |||||||
| chr12:48654260 | A | T | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1348-85T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 9/9 | chr12 | 48654260 | |||||||
| chr12:48654367 | G | T | 2 | a0002c0001t0001g0139 a0002c0001t0001g0140 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1348-192C>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 9/9 | chr12 | 48654367 | |||||||
| chr12:48654429 | A | G | 1 | a0002c0004t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1348-254T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 9/9 | chr12 | 48654429 | |||||||
| chr12:48654623 | G | A | 1 | a0001c0003t0001g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1347+318C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 9/9 | chr12 | 48654623 | |||||||
| chr12:48654723 | C | T | 2 | a0003c0005t0001g0029 a0003c0005t0001g0030 |
4 | HG00733.hp1 HG00735.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+218G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 9/9 | chr12 | 48654723 | |||||||
| chr12:48655202 | G | A | 139 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(136): Show |
187 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.1228-142C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48655202 | |||||||
| chr12:48655251 | C | A | 1 | a0002c0001t0001g0068 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1228-191G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48655251 | |||||||
| chr12:48655344 | A | G | 2 | a0001c0003t0002g0220 a0001c0003t0002g0239 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1228-284T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48655344 | |||||||
| chr12:48655430 | G | A | 7 | a0002c0004t0001g0010 a0002c0004t0001g0058 a0002c0004t0001g0059 others(4): Show |
9 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1228-370C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48655430 | |||||||
| chr12:48655568 | C | CA | 130 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(127): Show |
176 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.1228-509dupT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48655568 | |||||||
| chr12:48655568 | C | CAA | 10 | a0001c0002t0001g0179 a0001c0002t0001g0202 a0001c0003t0001g0060 others(7): Show |
12 | HG01952.hp2 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1228-510_1228-509d others(4): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48655568 | |||||||
| chr12:48655827 | G | A | 1 | a0002c0001t0001g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1228-767C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48655827 | |||||||
| chr12:48655930 | G | A | 3 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 |
4 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-870C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48655930 | |||||||
| chr12:48656088 | T | C | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1228-1028A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656088 | |||||||
| chr12:48656137 | C | A | 1 | a0001c0002t0001g0182 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1228-1077G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656137 | |||||||
| chr12:48656203 | T | C | 4 | a0002c0004t0001g0014 a0002c0004t0001g0046 a0002c0004t0001g0047 others(1): Show |
5 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1228-1143A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656203 | |||||||
| chr12:48656267 | T | G | 1 | a0001c0002t0001g0207 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1228-1207A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656267 | |||||||
| chr12:48656277 | G | GT | 26 | a0001c0002t0001g0168 a0001c0003t0002g0037 a0001c0003t0002g0038 others(23): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1228-1218dupA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656277 | |||||||
| chr12:48656277 | GT | G | 11 | a0002c0001t0001g0008 a0002c0001t0001g0106 a0002c0001t0001g0134 others(8): Show |
15 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1228-1218delA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656277 | |||||||
| chr12:48656282 | T | G | 1 | a0002c0001t0001g0077 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1228-1222A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656282 | |||||||
| chr12:48656283 | T | G | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1228-1223A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656283 | |||||||
| chr12:48656335 | G | A | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1228-1275C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656335 | |||||||
| chr12:48656337 | G | A | 1 | a0001c0002t0001g0181 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1228-1277C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656337 | |||||||
| chr12:48656399 | C | A | 128 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(125): Show |
175 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.1228-1339G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656399 | |||||||
| chr12:48656422 | T | C | 3 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 |
4 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1228-1362A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656422 | |||||||
| chr12:48656495 | G | A | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1228-1435C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656495 | |||||||
| chr12:48656610 | T | TA | 17 | a0001c0002t0001g0172 a0001c0002t0001g0210 a0001c0002t0001g0215 others(14): Show |
18 | HG00741.hp1 HG00741.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1228-1551dupT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656610 | |||||||
| chr12:48656610 | TA | T | 5 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 others(2): Show |
6 | HG01109.hp1 HG01168.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1228-1551delT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656610 | |||||||
| chr12:48656631 | T | A | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1228-1571A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656631 | |||||||
| chr12:48656972 | G | A | 1 | a0002c0001t0001g0094 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1228-1912C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656972 | |||||||
| chr12:48656996 | G | T | 5 | a0002c0004t0001g0010 a0002c0004t0001g0136 a0002c0004t0001g0141 others(2): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1228-1936C>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48656996 | |||||||
| chr12:48657268 | T | C | 7 | a0002c0004t0001g0010 a0002c0004t0001g0058 a0002c0004t0001g0059 others(4): Show |
9 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1228-2208A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657268 | |||||||
| chr12:48657411 | C | G | 1 | a0001c0002t0001g0161 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1228-2351G>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657411 | |||||||
| chr12:48657415 | ACT | A | 3 | a0002c0001t0001g0115 a0002c0001t0001g0116 a0002c0001t0001g0118 |
3 | HG02056.hp2 HG02735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1228-2357_1228-235 others(6): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657415 | |||||||
| chr12:48657473 | G | A | 1 | a0002c0001t0001g0106 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1228-2413C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657473 | |||||||
| chr12:48657500 | AT | A | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1228-2441delA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657500 | |||||||
| chr12:48657604 | T | TTG | 2 | a0001c0002t0001g0003 a0001c0002t0001g0177 |
3 | NA19060.hp1 NA19060.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.1228-2546_1228-254 others(6): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657604 | |||||||
| chr12:48657604 | TTG | T | 41 | a0001c0003t0001g0060 a0001c0003t0001g0121 a0001c0003t0002g0037 others(38): Show |
46 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.1228-2546_1228-254 others(6): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657604 | |||||||
| chr12:48657606 | G | C | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1228-2546C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657606 | |||||||
| chr12:48657625 | C | A | 1 | a0001c0002t0001g0150 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1228-2565G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657625 | |||||||
| chr12:48657761 | C | T | 1 | a0002c0001t0001g0024 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1227+2605G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657761 | |||||||
| chr12:48657824 | C | T | 3 | a0002c0001t0001g0057 a0002c0001t0001g0111 a0002c0001t0001g0112 |
3 | NA18955.hp2 NA18973.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1227+2542G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657824 | |||||||
| chr12:48657907 | G | A | 1 | a0002c0004t0001g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1227+2459C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657907 | |||||||
| chr12:48657910 | C | T | 1 | a0003c0005t0001g0029 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1227+2456G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657910 | |||||||
| chr12:48657959 | G | T | 2 | a0002c0001t0001g0009 a0002c0001t0001g0056 |
4 | HG02886.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1227+2407C>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657959 | |||||||
| chr12:48657986 | T | C | 1 | a0001c0003t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1227+2380A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48657986 | |||||||
| chr12:48658014 | T | G | 1 | a0001c0002t0001g0209 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1227+2352A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658014 | |||||||
| chr12:48658187 | C | T | 3 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 |
4 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1227+2179G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658187 | |||||||
| chr12:48658333 | CAT | C | 3 | a0002c0004t0001g0010 a0002c0004t0001g0141 a0002c0004t0001g0143 |
5 | HG02451.hp1 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1227+2031_1227+203 others(6): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658333 | |||||||
| chr12:48658480 | C | T | 1 | a0001c0002t0001g0216 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1227+1886G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658480 | |||||||
| chr12:48658482 | C | T | 1 | a0001c0002t0001g0169 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1227+1884G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658482 | |||||||
| chr12:48658572 | A | G | 1 | a0001c0002t0001g0178 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1227+1794T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658572 | |||||||
| chr12:48658582 | C | T | 1 | a0001c0002t0001g0147 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1227+1784G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658582 | |||||||
| chr12:48658790 | C | T | 1 | a0002c0004t0001g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1227+1576G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658790 | |||||||
| chr12:48658948 | T | C | 1 | a0002c0001t0001g0079 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1227+1418A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658948 | |||||||
| chr12:48658953 | A | G | 26 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(23): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1227+1413T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658953 | |||||||
| chr12:48658975 | G | A | 135 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(132): Show |
181 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.1227+1391C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48658975 | |||||||
| chr12:48659012 | C | G | 138 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(135): Show |
184 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1227+1354G>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659012 | |||||||
| chr12:48659276 | A | G | 1 | a0001c0002t0001g0146 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1227+1090T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659276 | |||||||
| chr12:48659278 | A | C | 1 | a0001c0002t0001g0011 | 3 | NA18960.hp2 NA18984.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1227+1088T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659278 | |||||||
| chr12:48659330 | T | C | 1 | a0002c0004t0001g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1227+1036A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659330 | |||||||
| chr12:48659359 | G | GGAGGCCA others(17): Show |
1 | a0001c0003t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1227+983_1227+1006 others(27): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659359 | |||||||
| chr12:48659448 | A | C | 1 | a0002c0001t0001g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1227+918T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659448 | |||||||
| chr12:48659623 | A | T | 15 | a0001c0002t0001g0011 a0002c0001t0001g0007 a0002c0001t0001g0053 others(12): Show |
18 | HG02055.hp2 HG02056.hp2 HG02735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1227+743T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659623 | |||||||
| chr12:48659664 | G | C | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1227+702C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659664 | |||||||
| chr12:48659741 | C | G | 1 | a0001c0002t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1227+625G>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659741 | |||||||
| chr12:48659980 | G | C | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1227+386C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659980 | |||||||
| chr12:48659999 | T | C | 1 | a0002c0004t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1227+367A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48659999 | |||||||
| chr12:48660310 | A | G | 1 | a0002c0004t0001g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1227+56T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 8/9 | chr12 | 48660310 | |||||||
| chr12:48660708 | G | C | 138 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(135): Show |
184 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.974-89C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48660708 | |||||||
| chr12:48660767 | A | G | 1 | a0001c0003t0002g0225 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.974-148T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48660767 | |||||||
| chr12:48660922 | C | T | 9 | a0002c0004t0001g0014 a0002c0004t0001g0041 a0002c0004t0001g0042 others(6): Show |
10 | HG01346.hp1 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.974-303G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48660922 | |||||||
| chr12:48660932 | C | T | 90 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(87): Show |
130 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.974-313G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48660932 | |||||||
| chr12:48661195 | CT | C | 83 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0012 others(80): Show |
116 | HG00323.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.974-577delA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661195 | |||||||
| chr12:48661282 | G | GAA | 4 | a0002c0004t0001g0010 a0002c0004t0001g0141 a0002c0004t0001g0142 others(1): Show |
6 | HG02257.hp2 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-665_974-664dup others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661282 | |||||||
| chr12:48661282 | GA | G | 26 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(23): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.974-664delT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661282 | |||||||
| chr12:48661283 | A | G | 3 | a0002c0001t0001g0002 a0002c0001t0001g0120 a0002c0001t0001g0128 |
3 | HG00558.hp1 NA18960.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.974-664T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661283 | |||||||
| chr12:48661324 | A | G | 1 | a0002c0001t0001g0102 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.974-705T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661324 | |||||||
| chr12:48661396 | C | T | 136 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(133): Show |
182 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.974-777G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661396 | |||||||
| chr12:48661402 | T | G | 1 | a0002c0001t0001g0127 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.974-783A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661402 | |||||||
| chr12:48661507 | T | C | 1 | a0002c0001t0001g0102 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.974-888A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661507 | |||||||
| chr12:48661629 | T | C | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG01346.hp1 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.974-1010A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661629 | |||||||
| chr12:48661672 | G | A | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.974-1053C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661672 | |||||||
| chr12:48661767 | A | G | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.974-1148T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48661767 | |||||||
| chr12:48662004 | G | A | 1 | a0002c0001t0001g0127 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.974-1385C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48662004 | |||||||
| chr12:48662010 | T | C | 1 | a0001c0002t0001g0166 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.974-1391A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48662010 | |||||||
| chr12:48662072 | T | C | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.974-1453A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48662072 | |||||||
| chr12:48662127 | C | T | 7 | a0002c0004t0001g0010 a0002c0004t0001g0058 a0002c0004t0001g0059 others(4): Show |
9 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.974-1508G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48662127 | |||||||
| chr12:48662352 | G | A | 8 | a0002c0004t0001g0010 a0002c0004t0001g0041 a0002c0004t0001g0042 others(5): Show |
10 | HG01346.hp1 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.974-1733C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48662352 | |||||||
| chr12:48662422 | G | A | 4 | a0002c0004t0001g0010 a0002c0004t0001g0141 a0002c0004t0001g0142 others(1): Show |
6 | HG02257.hp2 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.974-1803C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48662422 | |||||||
| chr12:48662452 | T | C | 1 | a0002c0001t0001g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.974-1833A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48662452 | |||||||
| chr12:48662638 | G | A | 1 | a0001c0002t0001g0025 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.974-2019C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48662638 | |||||||
| chr12:48662880 | G | A | 26 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(23): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.974-2261C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48662880 | |||||||
| chr12:48663004 | G | A | 27 | a0001c0003t0001g0060 a0001c0003t0001g0121 a0001c0003t0002g0037 others(24): Show |
29 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.974-2385C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663004 | |||||||
| chr12:48663069 | T | C | 1 | a0002c0001t0001g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.974-2450A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663069 | |||||||
| chr12:48663088 | T | C | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.974-2469A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663088 | |||||||
| chr12:48663092 | A | C | 1 | a0002c0001t0001g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.974-2473T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663092 | |||||||
| chr12:48663119 | A | C | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.974-2500T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663119 | |||||||
| chr12:48663325 | A | G | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG01346.hp1 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.974-2706T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663325 | |||||||
| chr12:48663422 | T | C | 1 | a0001c0002t0001g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.974-2803A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663422 | |||||||
| chr12:48663488 | T | C | 1 | a0001c0002t0001g0206 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.974-2869A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663488 | |||||||
| chr12:48663546 | CAAT | C | 3 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 |
4 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-2930_974-2928d others(5): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663546 | |||||||
| chr12:48663562 | T | A | 4 | a0002c0004t0001g0014 a0002c0004t0001g0046 a0002c0004t0001g0047 others(1): Show |
5 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.974-2943A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663562 | |||||||
| chr12:48663752 | CT | C | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG01346.hp1 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.974-3134delA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663752 | |||||||
| chr12:48663779 | T | C | 1 | a0001c0002t0001g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.974-3160A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663779 | |||||||
| chr12:48663869 | G | A | 1 | a0001c0002t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.974-3250C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663869 | |||||||
| chr12:48663898 | C | T | 3 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 |
4 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-3279G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663898 | |||||||
| chr12:48663905 | C | T | 1 | a0001c0002t0001g0175 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.974-3286G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663905 | |||||||
| chr12:48663913 | C | CT | 65 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(62): Show |
91 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.974-3295dupA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663913 | |||||||
| chr12:48663913 | C | CTT | 13 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0034 others(10): Show |
14 | HG00597.hp2 HG00733.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.974-3296_974-3295d others(4): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663913 | |||||||
| chr12:48663913 | CT | C | 18 | a0001c0002t0001g0151 a0001c0002t0001g0152 a0001c0002t0003g0013 others(15): Show |
22 | HG01109.hp1 HG01257.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.974-3295delA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663913 | |||||||
| chr12:48663913 | CTT | C | 25 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(22): Show |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.974-3296_974-3295d others(4): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663913 | |||||||
| chr12:48663914 | T | G | 1 | a0002c0004t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.974-3295A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663914 | |||||||
| chr12:48663915 | T | G | 5 | a0002c0004t0001g0010 a0002c0004t0001g0059 a0002c0004t0001g0141 others(2): Show |
7 | HG02257.hp2 HG02451.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.974-3296A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663915 | |||||||
| chr12:48663916 | T | G | 1 | a0002c0004t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.974-3297A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663916 | |||||||
| chr12:48663918 | T | C | 3 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 |
4 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.974-3299A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663918 | |||||||
| chr12:48663922 | T | G | 1 | a0002c0004t0001g0059 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.974-3303A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663922 | |||||||
| chr12:48663939 | A | T | 1 | a0002c0004t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.974-3320T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663939 | |||||||
| chr12:48663967 | G | A | 1 | a0001c0002t0001g0166 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.974-3348C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48663967 | |||||||
| chr12:48664040 | G | T | 15 | a0001c0002t0001g0028 a0001c0002t0001g0147 a0001c0002t0001g0152 others(12): Show |
18 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.974-3421C>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664040 | |||||||
| chr12:48664089 | A | G | 5 | a0002c0004t0001g0010 a0002c0004t0001g0136 a0002c0004t0001g0141 others(2): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.974-3470T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664089 | |||||||
| chr12:48664216 | T | C | 1 | a0002c0004t0001g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.973+3477A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664216 | |||||||
| chr12:48664257 | C | T | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+3436G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664257 | |||||||
| chr12:48664279 | AT | A | 134 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(131): Show |
182 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.973+3413delA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664279 | |||||||
| chr12:48664373 | A | G | 135 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(132): Show |
183 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.973+3320T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664373 | |||||||
| chr12:48664468 | T | C | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG01346.hp1 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.973+3225A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664468 | |||||||
| chr12:48664480 | G | A | 1 | a0002c0001t0001g0122 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.973+3213C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664480 | |||||||
| chr12:48664530 | G | A | 1 | a0002c0001t0001g0140 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.973+3163C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664530 | |||||||
| chr12:48664577 | C | CT | 21 | a0002c0001t0001g0017 a0002c0001t0001g0063 a0002c0001t0001g0065 others(18): Show |
24 | HG00621.hp2 HG01243.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.973+3115dupA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664577 | |||||||
| chr12:48664577 | CT | C | 102 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(99): Show |
146 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.973+3115delA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664577 | |||||||
| chr12:48664577 | CTT | C | 11 | a0001c0002t0001g0152 a0001c0003t0001g0060 a0001c0003t0002g0222 others(8): Show |
11 | HG01346.hp1 HG01515.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.973+3114_973+3115d others(4): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664577 | |||||||
| chr12:48664577 | CTTT | C | 9 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 others(6): Show |
11 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.973+3113_973+3115d others(5): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664577 | |||||||
| chr12:48664619 | T | C | 91 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(88): Show |
133 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.973+3074A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664619 | |||||||
| chr12:48664798 | G | A | 1 | a0001c0002t0001g0025 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.973+2895C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664798 | |||||||
| chr12:48664860 | G | GT | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+2832dupA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664860 | |||||||
| chr12:48664872 | G | A | 4 | a0002c0001t0001g0021 a0002c0001t0001g0093 a0002c0001t0001g0095 others(1): Show |
5 | HG00621.hp2 NA18944.hp2 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.973+2821C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664872 | |||||||
| chr12:48664879 | C | CT | 54 | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0002t0001g0035 others(51): Show |
62 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.973+2813dupA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664879 | |||||||
| chr12:48664879 | C | CTT | 11 | a0001c0003t0002g0220 a0001c0003t0002g0237 a0001c0003t0002g0238 others(8): Show |
13 | HG01109.hp1 HG02056.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.973+2812_973+2813d others(4): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664879 | |||||||
| chr12:48664879 | C | CTTT | 13 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(10): Show |
15 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.973+2811_973+2813d others(5): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664879 | |||||||
| chr12:48664946 | G | C | 2 | a0002c0001t0001g0098 a0002c0001t0001g0099 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.973+2747C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664946 | |||||||
| chr12:48664953 | C | CCTAA | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+2739_973+2740i others(6): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48664953 | |||||||
| chr12:48665025 | G | A | 1 | a0002c0001t0001g0127 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.973+2668C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48665025 | |||||||
| chr12:48665031 | A | G | 91 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(88): Show |
133 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.973+2662T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48665031 | |||||||
| chr12:48665036 | ATTTTTCT others(6): Show |
A | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+2644_973+2656d others(15): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48665036 | |||||||
| chr12:48665127 | C | T | 1 | a0001c0002t0001g0199 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.973+2566G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48665127 | |||||||
| chr12:48665131 | C | G | 1 | a0002c0004t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.973+2562G>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48665131 | |||||||
| chr12:48665195 | A | C | 1 | a0001c0003t0002g0224 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.973+2498T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48665195 | |||||||
| chr12:48665297 | G | A | 1 | a0001c0002t0001g0164 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.973+2396C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48665297 | |||||||
| chr12:48665475 | A | G | 1 | a0002c0001t0001g0090 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.973+2218T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48665475 | |||||||
| chr12:48665649 | A | C | 1 | a0002c0001t0001g0110 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.973+2044T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48665649 | |||||||
| chr12:48665909 | T | A | 1 | a0002c0004t0001g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.973+1784A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48665909 | |||||||
| chr12:48666030 | T | C | 1 | a0001c0002t0001g0180 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.973+1663A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666030 | |||||||
| chr12:48666200 | G | C | 9 | a0002c0004t0001g0014 a0002c0004t0001g0041 a0002c0004t0001g0042 others(6): Show |
10 | HG01346.hp1 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+1493C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666200 | |||||||
| chr12:48666220 | A | T | 1 | a0002c0001t0001g0138 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.973+1473T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666220 | |||||||
| chr12:48666320 | G | A | 1 | a0002c0001t0001g0071 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.973+1373C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666320 | |||||||
| chr12:48666378 | T | C | 13 | a0001c0002t0001g0003 a0001c0002t0001g0031 a0001c0002t0001g0033 others(10): Show |
22 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.973+1315A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666378 | |||||||
| chr12:48666381 | A | C | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.973+1312T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666381 | |||||||
| chr12:48666395 | A | T | 1 | a0001c0003t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+1298T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666395 | |||||||
| chr12:48666399 | A | T | 1 | a0002c0001t0001g0024 | 2 | HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.973+1294T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666399 | |||||||
| chr12:48666402 | A | T | 1 | a0001c0002t0001g0173 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.973+1291T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666402 | |||||||
| chr12:48666452 | G | A | 26 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(23): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.973+1241C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666452 | |||||||
| chr12:48666521 | C | T | 26 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(23): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.973+1172G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666521 | |||||||
| chr12:48666554 | G | A | 1 | a0002c0001t0001g0100 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.973+1139C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666554 | |||||||
| chr12:48666587 | G | C | 1 | a0001c0003t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.973+1106C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666587 | |||||||
| chr12:48666726 | A | T | 1 | a0001c0002t0001g0031 | 2 | HG01261.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.973+967T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48666726 | |||||||
| chr12:48667059 | T | C | 1 | a0002c0001t0001g0083 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.973+634A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48667059 | |||||||
| chr12:48667082 | G | A | 7 | a0002c0001t0001g0009 a0002c0001t0001g0056 a0002c0001t0001g0104 others(4): Show |
9 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.973+611C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48667082 | |||||||
| chr12:48667191 | A | C | 1 | a0002c0001t0001g0124 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.973+502T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48667191 | |||||||
| chr12:48667223 | C | T | 1 | a0001c0002t0001g0208 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.973+470G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48667223 | |||||||
| chr12:48667315 | A | G | 1 | a0002c0001t0006g0133 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.973+378T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48667315 | |||||||
| chr12:48667453 | C | T | 1 | a0001c0002t0001g0012 | 3 | NA18961.hp1 NA18986.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.973+240G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 7/9 | chr12 | 48667453 | |||||||
| chr12:48668012 | T | G | 1 | a0002c0004t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.877-223A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668012 | |||||||
| chr12:48668157 | C | T | 1 | a0002c0001t0001g0114 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.877-368G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668157 | |||||||
| chr12:48668204 | C | T | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.877-415G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668204 | |||||||
| chr12:48668356 | T | A | 1 | a0002c0001t0001g0128 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.877-567A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668356 | |||||||
| chr12:48668555 | C | T | 1 | a0002c0004t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.876+551G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668555 | |||||||
| chr12:48668767 | C | A | 1 | a0002c0001t0001g0096 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.876+339G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668767 | |||||||
| chr12:48668779 | T | C | 5 | a0002c0001t0001g0104 a0002c0001t0001g0122 a0002c0001t0001g0130 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.876+327A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668779 | |||||||
| chr12:48668783 | T | C | 1 | a0002c0001t0001g0129 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.876+323A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668783 | |||||||
| chr12:48668869 | A | C | 15 | a0001c0002t0001g0028 a0001c0002t0001g0147 a0001c0002t0001g0152 others(12): Show |
18 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.876+237T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668869 | |||||||
| chr12:48668880 | A | G | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.876+226T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668880 | |||||||
| chr12:48668929 | G | A | 7 | a0002c0004t0001g0010 a0002c0004t0001g0058 a0002c0004t0001g0059 others(4): Show |
9 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.876+177C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48668929 | |||||||
| chr12:48669059 | A | G | 1 | a0001c0002t0001g0185 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.876+47T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48669059 | |||||||
| chr12:48669088 | G | A | 1 | a0002c0001t0001g0116 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.876+18C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48669088 | |||||||
| chr12:48669089 | G | T | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.876+17C>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48669089 | |||||||
| chr12:48669096 | C | T | 1 | a0001c0002t0001g0166 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.876+10G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 6/9 | chr12 | 48669096 | |||||||
| chr12:48669329 | C | G | 1 | a0002c0001t0001g0089 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.710-57G>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48669329 | |||||||
| chr12:48669439 | C | T | 1 | a0001c0003t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.710-167G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48669439 | |||||||
| chr12:48669521 | A | T | 133 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(130): Show |
179 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.710-249T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48669521 | |||||||
| chr12:48669612 | G | A | 1 | a0001c0003t0002g0238 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.710-340C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48669612 | |||||||
| chr12:48669615 | T | C | 5 | a0002c0004t0001g0010 a0002c0004t0001g0136 a0002c0004t0001g0141 others(2): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.710-343A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48669615 | |||||||
| chr12:48669678 | C | T | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.710-406G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48669678 | |||||||
| chr12:48669805 | G | A | 2 | a0001c0003t0002g0221 a0001c0003t0002g0222 |
2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.710-533C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48669805 | |||||||
| chr12:48669873 | G | A | 1 | a0002c0001t0001g0128 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.710-601C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48669873 | |||||||
| chr12:48670053 | T | C | 1 | a0002c0004t0001g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.710-781A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48670053 | |||||||
| chr12:48670198 | C | CA | 10 | a0001c0002t0001g0157 a0001c0003t0002g0235 a0002c0001t0001g0105 others(7): Show |
12 | HG00544.hp2 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.710-927dupT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48670198 | |||||||
| chr12:48670198 | C | CAA | 93 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(90): Show |
134 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.710-928_710-927dup others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48670198 | |||||||
| chr12:48670461 | G | A | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.710-1189C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48670461 | |||||||
| chr12:48670463 | T | C | 26 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(23): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.710-1191A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48670463 | |||||||
| chr12:48670554 | T | A | 1 | a0002c0004t0001g0041 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.709+1245A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48670554 | |||||||
| chr12:48670592 | A | T | 1 | a0002c0001t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.709+1207T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48670592 | |||||||
| chr12:48670676 | T | A | 93 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(90): Show |
134 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.709+1123A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48670676 | |||||||
| chr12:48670840 | A | G | 1 | a0002c0001t0001g0088 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.709+959T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48670840 | |||||||
| chr12:48670997 | C | A | 1 | a0001c0002t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.709+802G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48670997 | |||||||
| chr12:48671063 | G | A | 1 | a0002c0004t0001g0042 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.709+736C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671063 | |||||||
| chr12:48671091 | C | G | 2 | a0002c0001t0001g0019 a0002c0001t0001g0087 |
3 | NA18974.hp1 NA19079.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.709+708G>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671091 | |||||||
| chr12:48671266 | G | A | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.709+533C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671266 | |||||||
| chr12:48671274 | T | TAA | 85 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(82): Show |
124 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.709+523_709+524dup others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671274 | |||||||
| chr12:48671274 | T | TAAA | 9 | a0001c0002t0001g0036 a0001c0002t0001g0185 a0001c0002t0001g0190 others(6): Show |
11 | HG00621.hp1 HG00639.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.709+522_709+524dup others(3): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671274 | |||||||
| chr12:48671274 | T | TAAAA | 25 | a0001c0003t0002g0037 a0001c0003t0002g0219 a0001c0003t0002g0220 others(22): Show |
28 | HG00099.hp2 HG01099.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.709+521_709+524dup others(4): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671274 | |||||||
| chr12:48671274 | T | TAAAAA | 7 | a0001c0003t0001g0060 a0001c0003t0001g0121 a0001c0003t0002g0038 others(4): Show |
8 | HG00323.hp1 HG02559.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.709+520_709+524dup others(5): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671274 | |||||||
| chr12:48671274 | T | TTAA | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG01346.hp1 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.709+524_709+525ins others(3): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671274 | |||||||
| chr12:48671486 | T | G | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG01346.hp1 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.709+313A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671486 | |||||||
| chr12:48671629 | G | A | 4 | a0002c0004t0001g0014 a0002c0004t0001g0046 a0002c0004t0001g0047 others(1): Show |
5 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.709+170C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671629 | |||||||
| chr12:48671672 | C | T | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.709+127G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 5/9 | chr12 | 48671672 | |||||||
| chr12:48672106 | T | C | 1 | a0001c0002t0001g0186 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.546-144A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672106 | |||||||
| chr12:48672128 | CAA | C | 9 | a0002c0004t0001g0014 a0002c0004t0001g0041 a0002c0004t0001g0042 others(6): Show |
10 | HG01346.hp1 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.546-168_546-167del others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672128 | |||||||
| chr12:48672366 | TGTATATA others(3): Show |
T | 1 | a0001c0003t0001g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.546-414_546-405del others(10): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672366 | |||||||
| chr12:48672367 | G | A | 16 | a0002c0004t0001g0010 a0002c0004t0001g0014 a0002c0004t0001g0041 others(13): Show |
19 | HG01346.hp1 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.546-405C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672367 | |||||||
| chr12:48672374 | T | C | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.546-412A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672374 | |||||||
| chr12:48672393 | G | GTA | 3 | a0002c0004t0001g0010 a0002c0004t0001g0141 a0002c0004t0001g0143 |
5 | HG02451.hp1 HG03098.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.546-433_546-432dup others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672393 | |||||||
| chr12:48672393 | G | GTATATAT others(25): Show |
1 | a0002c0004t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.546-432_546-431ins others(32): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672393 | |||||||
| chr12:48672393 | G | GTATATAT others(33): Show |
1 | a0002c0004t0001g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.546-432_546-431ins others(40): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672393 | |||||||
| chr12:48672393 | G | GTATATAT others(35): Show |
1 | a0002c0004t0001g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.546-432_546-431ins others(42): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672393 | |||||||
| chr12:48672395 | A | G | 1 | a0001c0002t0001g0028 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.546-433T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672395 | |||||||
| chr12:48672406 | T | C | 1 | a0001c0002t0001g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.546-444A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672406 | |||||||
| chr12:48672409 | G | GTA | 62 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(59): Show |
95 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.546-449_546-448dup others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672409 | |||||||
| chr12:48672409 | G | GTATA | 7 | a0001c0002t0001g0026 a0001c0002t0001g0034 a0001c0002t0001g0188 others(4): Show |
9 | HG00323.hp2 HG01361.hp2 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.546-451_546-448dup others(4): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672409 | |||||||
| chr12:48672409 | G | GTATATA | 4 | a0001c0002t0001g0189 a0001c0002t0001g0190 a0001c0002t0001g0194 others(1): Show |
4 | HG01928.hp1 HG02523.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.546-453_546-448dup others(6): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672409 | |||||||
| chr12:48672410 | T | TGC | 2 | a0002c0004t0001g0014 a0002c0004t0001g0048 |
3 | HG02965.hp1 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.546-449_546-448ins others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672410 | |||||||
| chr12:48672411 | A | G | 3 | a0002c0001t0006g0133 a0002c0004t0001g0058 a0002c0004t0001g0059 |
3 | HG02970.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.546-449T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672411 | |||||||
| chr12:48672423 | A | ACG | 2 | a0002c0004t0001g0014 a0002c0004t0001g0048 |
3 | HG02965.hp1 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.546-462_546-461ins others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672423 | |||||||
| chr12:48672426 | TA | T | 8 | a0001c0003t0002g0220 a0001c0003t0002g0232 a0001c0003t0002g0233 others(5): Show |
8 | HG01516.hp2 HG01517.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-465delT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672426 | |||||||
| chr12:48672428 | TA | T | 14 | a0001c0003t0002g0037 a0001c0003t0002g0038 a0001c0003t0002g0219 others(11): Show |
16 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.546-467delT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672428 | |||||||
| chr12:48672429 | A | AT | 7 | a0001c0002t0001g0011 a0002c0001t0001g0002 a0002c0001t0001g0015 others(4): Show |
8 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-468dupA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672429 | |||||||
| chr12:48672429 | A | ATT | 9 | a0001c0002t0001g0011 a0002c0001t0001g0007 a0002c0001t0001g0053 others(6): Show |
11 | HG02735.hp1 NA18942.hp2 NA18960.hp2 others(8): Show |
intron_variant | MODIFIER | c.546-468_546-467ins others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672429 | |||||||
| chr12:48672429 | A | T | 10 | a0001c0003t0002g0220 a0001c0003t0002g0232 a0001c0003t0002g0233 others(7): Show |
10 | HG01516.hp2 HG01517.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.546-467T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672429 | |||||||
| chr12:48672430 | TA | T | 13 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0003t0002g0224 others(10): Show |
14 | HG01109.hp1 HG01255.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.546-469delT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672430 | |||||||
| chr12:48672431 | A | ATT | 8 | a0002c0001t0001g0002 a0002c0001t0001g0024 a0002c0001t0001g0081 others(5): Show |
9 | HG00558.hp1 HG02055.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.546-470_546-469ins others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672431 | |||||||
| chr12:48672431 | A | ATTTT | 2 | a0002c0001t0001g0008 a0002c0001t0001g0134 |
4 | HG02717.hp1 HG03041.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-470_546-469ins others(4): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672431 | |||||||
| chr12:48672431 | A | T | 83 | a0001c0002t0001g0011 a0001c0003t0002g0037 a0001c0003t0002g0038 others(80): Show |
105 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.546-469T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672431 | |||||||
| chr12:48672433 | A | ATATATAT others(39): Show |
1 | a0002c0004t0001g0014 | 2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.546-472_546-471ins others(46): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672433 | |||||||
| chr12:48672433 | A | ATATATAT others(39): Show |
1 | a0002c0004t0001g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.546-472_546-471ins others(46): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672433 | |||||||
| chr12:48672433 | A | ATATATAT others(35): Show |
1 | a0001c0003t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.546-472_546-471ins others(42): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672433 | |||||||
| chr12:48672433 | A | ATT | 11 | a0001c0002t0001g0012 a0001c0002t0001g0027 a0001c0002t0001g0036 others(8): Show |
15 | HG00438.hp1 HG00621.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.546-473_546-472dup others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672433 | |||||||
| chr12:48672433 | A | T | 122 | a0001c0002t0001g0011 a0001c0002t0003g0013 a0001c0002t0003g0040 others(119): Show |
153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.546-471T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672433 | |||||||
| chr12:48672435 | T | A | 2 | a0001c0002t0001g0211 a0001c0002t0001g0214 |
2 | HG00323.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.546-473A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672435 | |||||||
| chr12:48672456 | C | T | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.546-494G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672456 | |||||||
| chr12:48672509 | T | C | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG01346.hp1 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.546-547A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672509 | |||||||
| chr12:48672584 | C | T | 1 | a0001c0002t0001g0146 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.546-622G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672584 | |||||||
| chr12:48672704 | G | A | 1 | a0001c0002t0001g0191 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.546-742C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672704 | |||||||
| chr12:48672767 | A | AT | 7 | a0002c0004t0001g0010 a0002c0004t0001g0058 a0002c0004t0001g0059 others(4): Show |
9 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.546-806dupA | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672767 | |||||||
| chr12:48672790 | GCT | G | 5 | a0002c0004t0001g0010 a0002c0004t0001g0136 a0002c0004t0001g0141 others(2): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.546-830_546-829del others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672790 | |||||||
| chr12:48672845 | G | A | 1 | a0001c0002t0001g0212 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.546-883C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672845 | |||||||
| chr12:48672912 | C | A | 5 | a0002c0004t0001g0010 a0002c0004t0001g0136 a0002c0004t0001g0141 others(2): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.546-950G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672912 | |||||||
| chr12:48672996 | C | T | 1 | a0002c0001t0001g0062 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.546-1034G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48672996 | |||||||
| chr12:48673011 | G | A | 90 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(87): Show |
130 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.546-1049C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673011 | |||||||
| chr12:48673025 | G | C | 17 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0014 others(14): Show |
20 | HG01346.hp1 HG01884.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.546-1063C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673025 | |||||||
| chr12:48673065 | T | C | 1 | a0002c0001t0001g0107 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.546-1103A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673065 | |||||||
| chr12:48673141 | C | G | 2 | a0002c0001t0001g0139 a0002c0001t0001g0140 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.546-1179G>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673141 | |||||||
| chr12:48673157 | T | C | 7 | a0002c0004t0001g0010 a0002c0004t0001g0058 a0002c0004t0001g0059 others(4): Show |
9 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.546-1195A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673157 | |||||||
| chr12:48673197 | C | T | 1 | a0002c0001t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.546-1235G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673197 | |||||||
| chr12:48673285 | C | T | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.546-1323G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673285 | |||||||
| chr12:48673406 | G | A | 1 | a0002c0004t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.546-1444C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673406 | |||||||
| chr12:48673480 | A | C | 3 | a0002c0001t0001g0115 a0002c0001t0001g0116 a0002c0001t0001g0118 |
3 | HG02056.hp2 HG02735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.546-1518T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673480 | |||||||
| chr12:48673567 | G | GA | 5 | a0001c0002t0001g0146 a0001c0002t0001g0205 a0002c0001t0001g0022 others(2): Show |
6 | HG01993.hp2 HG02300.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.546-1606dupT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673567 | |||||||
| chr12:48673567 | GA | G | 13 | a0001c0002t0001g0152 a0001c0003t0001g0060 a0001c0003t0002g0223 others(10): Show |
15 | HG01099.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.546-1606delT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673567 | |||||||
| chr12:48673574 | A | G | 5 | a0002c0004t0001g0010 a0002c0004t0001g0136 a0002c0004t0001g0141 others(2): Show |
7 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.546-1612T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673574 | |||||||
| chr12:48673619 | T | A | 17 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0014 others(14): Show |
20 | HG01346.hp1 HG01884.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.546-1657A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673619 | |||||||
| chr12:48673663 | T | C | 1 | a0001c0003t0002g0236 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.546-1701A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673663 | |||||||
| chr12:48673784 | A | T | 1 | a0001c0002t0001g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.546-1822T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673784 | |||||||
| chr12:48673826 | C | T | 5 | a0002c0001t0001g0081 a0002c0001t0001g0083 a0002c0001t0001g0085 others(2): Show |
5 | HG02055.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.546-1864G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673826 | |||||||
| chr12:48673849 | A | G | 1 | a0002c0004t0001g0046 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.546-1887T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48673849 | |||||||
| chr12:48674027 | A | T | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.546-2065T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48674027 | |||||||
| chr12:48674234 | G | A | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.546-2272C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48674234 | |||||||
| chr12:48674401 | C | T | 1 | a0002c0001t0001g0114 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.546-2439G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48674401 | |||||||
| chr12:48674430 | G | A | 93 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(90): Show |
134 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.546-2468C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48674430 | |||||||
| chr12:48674451 | C | A | 138 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(135): Show |
184 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.546-2489G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48674451 | |||||||
| chr12:48674695 | G | A | 1 | a0001c0003t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.546-2733C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48674695 | |||||||
| chr12:48674905 | G | A | 3 | a0001c0002t0001g0192 a0001c0002t0001g0193 a0001c0002t0001g0194 |
3 | HG01081.hp2 HG01928.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.546-2943C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48674905 | |||||||
| chr12:48674983 | TAATAA | T | 3 | a0001c0002t0001g0156 a0001c0002t0001g0162 a0001c0002t0001g0195 |
3 | HG02486.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.546-3026_546-3022d others(7): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48674983 | |||||||
| chr12:48675023 | TAAAA | T | 38 | a0002c0001t0001g0002 a0002c0001t0001g0015 a0002c0001t0001g0019 others(35): Show |
53 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.546-3065_546-3062d others(6): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48675023 | |||||||
| chr12:48675105 | G | C | 26 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(23): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.546-3143C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48675105 | |||||||
| chr12:48675249 | G | A | 127 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(124): Show |
172 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.546-3287C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48675249 | |||||||
| chr12:48675329 | C | T | 1 | a0002c0001t0001g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.546-3367G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48675329 | |||||||
| chr12:48675363 | G | A | 2 | a0002c0001t0001g0139 a0002c0001t0001g0140 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.546-3401C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48675363 | |||||||
| chr12:48675391 | T | C | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.546-3429A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48675391 | |||||||
| chr12:48675663 | C | T | 1 | a0001c0003t0001g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.545+3373G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48675663 | |||||||
| chr12:48675716 | T | G | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.545+3320A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48675716 | |||||||
| chr12:48675742 | A | T | 1 | a0001c0003t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.545+3294T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48675742 | |||||||
| chr12:48675853 | T | C | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.545+3183A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48675853 | |||||||
| chr12:48676110 | T | G | 2 | a0002c0001t0001g0109 a0002c0001t0001g0123 |
2 | HG00544.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.545+2926A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48676110 | |||||||
| chr12:48676238 | G | C | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.545+2798C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48676238 | |||||||
| chr12:48676242 | A | G | 1 | a0001c0003t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.545+2794T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48676242 | |||||||
| chr12:48676424 | G | A | 1 | a0002c0001t0001g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.545+2612C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48676424 | |||||||
| chr12:48676455 | T | A | 1 | a0002c0001t0001g0061 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.545+2581A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48676455 | |||||||
| chr12:48676586 | A | G | 2 | a0002c0001t0001g0109 a0002c0001t0001g0123 |
2 | HG00544.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.545+2450T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48676586 | |||||||
| chr12:48676641 | A | C | 4 | a0002c0004t0001g0014 a0002c0004t0001g0046 a0002c0004t0001g0047 others(1): Show |
5 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+2395T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48676641 | |||||||
| chr12:48676673 | C | T | 1 | a0002c0001t0001g0085 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.545+2363G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48676673 | |||||||
| chr12:48676686 | C | T | 19 | a0001c0003t0002g0037 a0001c0003t0002g0038 a0001c0003t0002g0219 others(16): Show |
21 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.545+2350G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48676686 | |||||||
| chr12:48676698 | C | T | 17 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0014 others(14): Show |
20 | HG01346.hp1 HG01884.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.545+2338G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48676698 | |||||||
| chr12:48677038 | G | A | 7 | a0002c0004t0001g0010 a0002c0004t0001g0058 a0002c0004t0001g0059 others(4): Show |
9 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.545+1998C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677038 | |||||||
| chr12:48677088 | T | C | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.545+1948A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677088 | |||||||
| chr12:48677462 | T | C | 90 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(87): Show |
130 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.545+1574A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677462 | |||||||
| chr12:48677476 | C | T | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.545+1560G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677476 | |||||||
| chr12:48677548 | G | A | 1 | a0001c0002t0001g0206 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.545+1488C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677548 | |||||||
| chr12:48677578 | G | A | 2 | a0001c0002t0001g0152 a0001c0002t0001g0161 |
2 | NA18942.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.545+1458C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677578 | |||||||
| chr12:48677640 | G | T | 2 | a0002c0001t0001g0139 a0002c0001t0001g0140 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.545+1396C>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677640 | |||||||
| chr12:48677784 | C | CA | 85 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(82): Show |
124 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.545+1251dupT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677784 | |||||||
| chr12:48677784 | C | CAA | 18 | a0001c0002t0001g0035 a0001c0002t0001g0195 a0001c0002t0001g0196 others(15): Show |
19 | HG00323.hp2 HG00735.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.545+1250_545+1251d others(4): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677784 | |||||||
| chr12:48677784 | CA | C | 31 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(28): Show |
34 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.545+1251delT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677784 | |||||||
| chr12:48677784 | CAA | C | 6 | a0001c0003t0001g0060 a0002c0004t0001g0041 a0002c0004t0001g0042 others(3): Show |
6 | HG01346.hp1 HG01884.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.545+1250_545+1251d others(4): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677784 | |||||||
| chr12:48677784 | CAAAAAA | C | 4 | a0002c0004t0001g0010 a0002c0004t0001g0141 a0002c0004t0001g0142 others(1): Show |
6 | HG02257.hp2 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.545+1246_545+1251d others(8): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677784 | |||||||
| chr12:48677784 | CAAAAAAA others(4): Show |
C | 1 | a0001c0002t0001g0157 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.545+1241_545+1251d others(13): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677784 | |||||||
| chr12:48677784 | CAAAAAAA others(5): Show |
C | 2 | a0001c0003t0002g0221 a0001c0003t0002g0222 |
2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.545+1240_545+1251d others(14): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677784 | |||||||
| chr12:48677824 | T | C | 3 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 |
4 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+1212A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677824 | |||||||
| chr12:48677937 | T | G | 4 | a0002c0004t0001g0014 a0002c0004t0001g0046 a0002c0004t0001g0047 others(1): Show |
5 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+1099A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677937 | |||||||
| chr12:48677953 | G | A | 1 | a0001c0002t0001g0214 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.545+1083C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48677953 | |||||||
| chr12:48678031 | T | A | 1 | a0001c0002t0001g0207 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.545+1005A>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48678031 | |||||||
| chr12:48678457 | A | T | 1 | a0001c0002t0001g0156 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.545+579T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48678457 | |||||||
| chr12:48678503 | G | T | 3 | a0002c0001t0001g0081 a0002c0001t0001g0083 a0002c0004t0001g0136 |
3 | HG02630.hp1 HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.545+533C>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48678503 | |||||||
| chr12:48678531 | T | C | 1 | a0001c0003t0001g0121 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.545+505A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48678531 | |||||||
| chr12:48678851 | A | C | 1 | a0002c0001t0001g0082 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.545+185T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48678851 | |||||||
| chr12:48678881 | G | A | 2 | a0002c0001t0001g0139 a0002c0001t0001g0140 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.545+155C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48678881 | |||||||
| chr12:48678893 | T | C | 3 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 |
4 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+143A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48678893 | |||||||
| chr12:48678931 | T | C | 8 | a0001c0003t0001g0060 a0002c0004t0001g0010 a0002c0004t0001g0058 others(5): Show |
10 | HG02257.hp2 HG02451.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.545+105A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48678931 | |||||||
| chr12:48678946 | C | G | 2 | a0002c0004t0001g0058 a0002c0004t0001g0059 |
2 | HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.545+90G>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48678946 | |||||||
| chr12:48679011 | T | C | 4 | a0002c0001t0001g0018 a0002c0001t0001g0076 a0002c0001t0001g0077 others(1): Show |
5 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.545+25A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 4/9 | chr12 | 48679011 | |||||||
| chr12:48679260 | C | CA | 6 | a0001c0002t0003g0013 a0001c0002t0003g0040 a0001c0009t0003g0039 others(3): Show |
7 | HG01109.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.431-111dupT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 3/9 | chr12 | 48679260 | |||||||
| chr12:48679265 | A | C | 1 | a0001c0002t0001g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.431-115T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 3/9 | chr12 | 48679265 | |||||||
| chr12:48679373 | G | A | 25 | a0001c0003t0002g0037 a0001c0003t0002g0038 a0001c0003t0002g0219 others(22): Show |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.431-223C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 3/9 | chr12 | 48679373 | |||||||
| chr12:48679575 | A | T | 137 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(134): Show |
185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.430+80T>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 3/9 | chr12 | 48679575 | |||||||
| chr12:48679643 | G | T | 1 | a0001c0003t0002g0219 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.430+12C>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 3/9 | chr12 | 48679643 | |||||||
| chr12:48679841 | G | A | 1 | a0001c0002t0001g0208 | 1 | NA19084.hp2 | splice_region_variant&intron_variant | LOW | c.252-8C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48679841 | |||||||
| chr12:48679938 | A | G | 26 | a0001c0003t0001g0121 a0001c0003t0002g0037 a0001c0003t0002g0038 others(23): Show |
28 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.252-105T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48679938 | |||||||
| chr12:48679939 | T | C | 1 | a0001c0002t0001g0209 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.252-106A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48679939 | |||||||
| chr12:48680206 | G | C | 1 | a0002c0001t0001g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.252-373C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680206 | |||||||
| chr12:48680520 | C | T | 137 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(134): Show |
185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.252-687G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680520 | |||||||
| chr12:48680768 | G | A | 1 | a0002c0004t0001g0136 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.251+614C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680768 | |||||||
| chr12:48680793 | A | G | 1 | a0001c0002t0001g0154 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.251+589T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680793 | |||||||
| chr12:48680830 | T | C | 25 | a0001c0003t0002g0037 a0001c0003t0002g0038 a0001c0003t0002g0219 others(22): Show |
27 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.251+552A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680830 | |||||||
| chr12:48680848 | C | T | 4 | a0002c0004t0001g0014 a0002c0004t0001g0046 a0002c0004t0001g0047 others(1): Show |
5 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+534G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680848 | |||||||
| chr12:48680851 | G | A | 9 | a0001c0002t0001g0005 a0001c0002t0001g0025 a0001c0002t0001g0153 others(6): Show |
14 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.251+531C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680851 | |||||||
| chr12:48680972 | G | GC | 24 | a0001c0003t0001g0121 a0001c0003t0002g0241 a0002c0001t0001g0008 others(21): Show |
28 | HG00544.hp1 HG00597.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.251+409dupG | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680972 | |||||||
| chr12:48680976 | C | A | 1 | a0002c0004t0001g0045 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.251+406G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680976 | |||||||
| chr12:48680978 | C | G | 1 | a0002c0001t0001g0081 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.251+404G>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680978 | |||||||
| chr12:48680979 | C | A | 94 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(91): Show |
137 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.251+403G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680979 | |||||||
| chr12:48680980 | G | A | 33 | a0001c0003t0001g0060 a0001c0003t0002g0037 a0001c0003t0002g0038 others(30): Show |
37 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.251+402C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680980 | |||||||
| chr12:48680980 | G | C | 182 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(179): Show |
249 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.251+402C>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680980 | |||||||
| chr12:48680981 | C | A | 35 | a0001c0003t0001g0060 a0001c0003t0002g0037 a0001c0003t0002g0038 others(32): Show |
39 | HG00099.hp2 HG00323.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.251+401G>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48680981 | |||||||
| chr12:48681011 | T | C | 1 | a0001c0003t0001g0060 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.251+371A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48681011 | |||||||
| chr12:48681045 | C | T | 1 | a0002c0001t0001g0061 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.251+337G>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48681045 | |||||||
| chr12:48681071 | A | C | 4 | a0002c0004t0001g0014 a0002c0004t0001g0046 a0002c0004t0001g0047 others(1): Show |
5 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+311T>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48681071 | |||||||
| chr12:48681091 | G | A | 4 | a0002c0004t0001g0014 a0002c0004t0001g0046 a0002c0004t0001g0047 others(1): Show |
5 | HG02818.hp1 HG02965.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.251+291C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48681091 | |||||||
| chr12:48681118 | T | TA | 13 | a0001c0002t0001g0036 a0001c0002t0001g0215 a0001c0002t0001g0216 others(10): Show |
15 | HG00621.hp1 HG01175.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.251+263dupT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48681118 | |||||||
| chr12:48681118 | T | TAA | 5 | a0001c0002t0001g0218 a0002c0004t0001g0010 a0002c0004t0001g0043 others(2): Show |
7 | HG02257.hp2 HG02451.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.251+262_251+263dup others(2): Show |
KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48681118 | |||||||
| chr12:48681118 | TA | T | 22 | a0001c0002t0001g0025 a0001c0002t0001g0147 a0001c0002t0001g0148 others(19): Show |
24 | HG00099.hp1 HG00558.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.251+263delT | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48681118 | |||||||
| chr12:48681324 | T | C | 4 | a0002c0004t0001g0010 a0002c0004t0001g0141 a0002c0004t0001g0142 others(1): Show |
6 | HG02257.hp2 HG02451.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.251+58A>G | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48681324 | |||||||
| chr12:48681376 | A | G | 1 | a0001c0002t0001g0146 | 1 | NA18994.hp2 | splice_region_variant&intron_variant | LOW | c.251+6T>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 2/9 | chr12 | 48681376 | |||||||
| chr12:48681939 | G | A | 1 | a0002c0001t0001g0144 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-10+248C>T | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 1/9 | chr12 | 48681939 | |||||||
| chr12:48682028 | T | G | 94 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0005 others(91): Show |
137 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.-10+159A>C | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 1/9 | chr12 | 48682028 | |||||||
| chr12:48682061 | G | T | 3 | a0002c0004t0001g0041 a0002c0004t0001g0042 a0002c0004t0001g0043 |
3 | HG01346.hp1 HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-10+126C>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 1/9 | chr12 | 48682061 | |||||||
| chr12:48682135 | G | T | 9 | a0002c0004t0001g0014 a0002c0004t0001g0041 a0002c0004t0001g0042 others(6): Show |
10 | HG01346.hp1 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-10+52C>A | KANSL2 | ENSG00000139620.13 | transcript | ENST00000420613.7 | protein_coding | 1/9 | chr12 | 48682135 |