Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84108 |
| ensemblid | ENSG00000156374.16 |
| hgncid | 21156 |
| symbol | PCGF6 |
| name | polycomb group ring finger 6 |
| refseq_nuc | NM_001011663.2 |
| refseq_prot | NP_001011663.1 |
| ensembl_nuc | ENST00000369847.4 |
| ensembl_prot | ENSP00000358862.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 103302796 |
| end | 103351140 |
| strand | - |
| ver | v1.2 |
| region | chr10:103302796-103351140 |
| region5000 | chr10:103297796-103356140 |
| regionname0 | PCGF6_chr10_103302796_103351140 |
| regionname5000 | PCGF6_chr10_103297796_103356140 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 350 | 200 | 64 | 39 | 83 | 6 | 7 | 57 | PCGF6_chr10_103297796_103356140 | PCGF6 | MEGVA others(345): Show |
chr10 | 103297796 | 103356140 |
| a0002 | 0/1 | 352 | 171 | 27 | 31 | 77 | 10 | 25 | 59 | PCGF6_chr10_103297796_103356140 | PCGF6 | MEGVA others(347): Show |
chr10 | 103297796 | 103356140 |
| a0003 | 0/0 | 350 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | MEGVA others(345): Show |
chr10 | 103297796 | 103356140 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1050 | 200 | 64 | 39 | 83 | 6 | 7 | PCGF6_chr10_103297796_103356140 | PCGF6 | ATGGA others(1045): Show |
chr10 | 103297796 | 103356140 | ||
| a0002c0002 | 0/1 | 1056 | 169 | 26 | 31 | 77 | 10 | 24 | PCGF6_chr10_103297796_103356140 | PCGF6 | ATGGA others(1051): Show |
chr10 | 103297796 | 103356140 | ||
| a0002c0003 | 0/0 | 1056 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | ATGGA others(1051): Show |
chr10 | 103297796 | 103356140 | ||
| a0002c0004 | 0/0 | 1056 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | ATGGA others(1051): Show |
chr10 | 103297796 | 103356140 | ||
| a0003c0005 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | ATGGA others(1045): Show |
chr10 | 103297796 | 103356140 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2236 | 181 | 48 | 36 | 83 | 6 | 7 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2231): Show |
chr10 | 103297796 | 103356140 |
| a0001c0001t0003 | 0/0 | 2236 | 18 | 15 | 3 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2231): Show |
chr10 | 103297796 | 103356140 |
| a0001c0001t0008 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2231): Show |
chr10 | 103297796 | 103356140 |
| a0002c0002t0001 | 0/1 | 2242 | 132 | 23 | 23 | 55 | 8 | 22 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2237): Show |
chr10 | 103297796 | 103356140 |
| a0002c0002t0002 | 0/0 | 2242 | 19 | 1 | 8 | 6 | 2 | 2 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2237): Show |
chr10 | 103297796 | 103356140 |
| a0002c0002t0004 | 0/0 | 2242 | 15 | 0 | 0 | 15 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2237): Show |
chr10 | 103297796 | 103356140 |
| a0002c0002t0005 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2237): Show |
chr10 | 103297796 | 103356140 |
| a0002c0002t0006 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2237): Show |
chr10 | 103297796 | 103356140 |
| a0002c0002t0007 | 0/0 | 2242 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2237): Show |
chr10 | 103297796 | 103356140 |
| a0002c0003t0002 | 0/0 | 2242 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2237): Show |
chr10 | 103297796 | 103356140 |
| a0002c0004t0001 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2237): Show |
chr10 | 103297796 | 103356140 |
| a0003c0005t0003 | 0/0 | 2236 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | AGTGG others(2231): Show |
chr10 | 103297796 | 103356140 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0004 | 0/0 | 3 | 1 | 0 | 1 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0231 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0001c0001t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0002t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0002c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| a0003c0005t0003g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0034 | EUR | GBR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | GBR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0144 | EUR | GBR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0170 | EUR | FIN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | FIN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00323 | hp2 | a0002 | c0002 | t0002 | g0132 | EUR | FIN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00423 | hp1 | a0002 | c0002 | t0004 | g0020 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0040 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0128 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0163 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0151 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0127 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0134 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0145 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0130 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0135 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0133 | EUR | IBS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0067 | EUR | IBS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0068 | EUR | IBS | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0042 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0330 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0174 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0116 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0351 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0140 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | CDX | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | CDX | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CDX | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02257 | hp1 | a0002 | c0002 | t0006 | g0089 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0121 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PEL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0141 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0122 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02723 | hp1 | a0003 | c0005 | t0003 | g0355 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0091 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0137 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02922 | hp1 | a0001 | c0001 | t0008 | g0221 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0021 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0131 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0160 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0062 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0165 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03491 | hp2 | a0002 | c0002 | t0001 | g0053 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | GWD | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03654 | hp2 | a0002 | c0003 | t0002 | g0136 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0153 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0108 | SAS | PJL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0056 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0123 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03927 | hp2 | a0002 | c0002 | t0001 | g0117 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0154 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0094 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0113 | SAS | STU | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0087 | SAS | STU | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0043 | SAS | BEB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0081 | SAS | STU | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | STU | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | CHB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | CHB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18940 | hp1 | a0002 | c0002 | t0004 | g0027 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18943 | hp2 | a0002 | c0002 | t0004 | g0035 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18945 | hp1 | a0002 | c0002 | t0004 | g0026 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18946 | hp2 | a0002 | c0002 | t0004 | g0024 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18953 | hp2 | a0002 | c0002 | t0004 | g0047 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18962 | hp1 | a0002 | c0002 | t0004 | g0031 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18963 | hp2 | a0002 | c0002 | t0004 | g0016 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0029 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18977 | hp2 | a0002 | c0002 | t0004 | g0030 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18982 | hp1 | a0002 | c0002 | t0004 | g0077 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18983 | hp1 | a0002 | c0002 | t0004 | g0028 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18984 | hp1 | a0002 | c0002 | t0004 | g0036 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18990 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18993 | hp1 | a0002 | c0002 | t0004 | g0039 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19011 | hp2 | a0002 | c0002 | t0007 | g0085 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0045 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19081 | hp1 | a0002 | c0002 | t0004 | g0025 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | YRI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA20129 | hp1 | a0002 | c0004 | t0001 | g0013 | AFR | ASW | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | ASW | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | TSI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA20805 | hp2 | a0002 | c0002 | t0001 | g0037 | EUR | TSI | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02109 | hp1 | a0002 | c0002 | t0005 | g0012 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | USA | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | USA | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | USA | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | USA | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | LWK | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0098 | REF | REF | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0231 | REF | REF | PCGF6_chr10_103297796_103356140 | PCGF6 | chr10 | 103297796 | 103356140 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:103326595 | G | A | 1 | a0002 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.848C>T | p.Ala283Val | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/10 | 922/2236 | 848/1053 | 283/350 | chr10 | 103326595 | |||
| chr10:103350766 | T | A | 1 | a0003 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.301A>T | p.Met101Leu | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/10 | 375/2236 | 301/1053 | 101/350 | chr10 | 103350766 | |||
| chr10:103350983 | A | AGGAGGC | 1 | a0002 | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
disruptive_inframe_insertion | MODERATE | c.78_83dupGCCTCC | p.Pro27_Pro28dup | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/10 | 157/2236 | 83/1053 | 28/350 | chr10 | 103350983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:103348946 | T | C | 1 | a0002c0004 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.414A>G | p.Lys138Lys | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 2/10 | 488/2236 | 414/1053 | 138/350 | chr10 | 103348946 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:103302929 | G | A | 2 | a0001c0001t0003 a0003c0005t0003 |
19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*976C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 976 | chr10 | 103302929 | ||||||
| chr10:103303099 | A | G | 1 | a0002c0002t0007 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*806T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 806 | chr10 | 103303099 | ||||||
| chr10:103303339 | C | A | 1 | a0001c0001t0008 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*566G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 566 | chr10 | 103303339 | ||||||
| chr10:103303522 | T | C | 2 | a0002c0002t0002 a0002c0003t0002 |
20 | HG00323.hp2 HG00733.hp1 HG00741.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*383A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 383 | chr10 | 103303522 | ||||||
| chr10:103303866 | G | T | 1 | a0002c0002t0006 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 39 | chr10 | 103303866 | ||||||
| chr10:103303879 | C | T | 1 | a0002c0002t0004 | 15 | HG00423.hp1 NA18940.hp1 NA18943.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*26G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 10/10 | 26 | chr10 | 103303879 | ||||||
| chr10:103351099 | C | T | 1 | a0002c0002t0005 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/10 | 33 | chr10 | 103351099 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:103304046 | T | C | 1 | a0003c0005t0003g0355 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.997-85A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304046 | |||||||
| chr10:103304140 | C | CT | 172 | a0001c0001t0001g0241 a0001c0001t0001g0248 a0001c0001t0001g0312 others(169): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.997-180dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304140 | |||||||
| chr10:103304537 | T | C | 169 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(166): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.997-576A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304537 | |||||||
| chr10:103304656 | C | CT | 343 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(340): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.997-696dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304656 | |||||||
| chr10:103304656 | C | CTT | 6 | a0001c0001t0001g0185 a0001c0001t0001g0216 a0002c0002t0001g0050 others(3): Show |
6 | HG00621.hp2 HG02258.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.997-697_997-696dup others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304656 | |||||||
| chr10:103304758 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.997-797G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304758 | |||||||
| chr10:103304854 | C | T | 2 | a0001c0001t0001g0306 a0001c0001t0001g0317 |
2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.997-893G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304854 | |||||||
| chr10:103304888 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.997-927C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103304888 | |||||||
| chr10:103305058 | G | A | 2 | a0001c0001t0001g0271 a0001c0001t0001g0273 |
2 | NA18957.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.997-1097C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305058 | |||||||
| chr10:103305140 | A | T | 1 | a0002c0002t0004g0020 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.997-1179T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305140 | |||||||
| chr10:103305140 | ATT | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(19): Show |
24 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.997-1181_997-1180d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305140 | |||||||
| chr10:103305216 | AC | A | 97 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0072 others(94): Show |
100 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.997-1256delG | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305216 | |||||||
| chr10:103305217 | C | G | 1 | a0002c0002t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.997-1256G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305217 | |||||||
| chr10:103305442 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.997-1481G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305442 | |||||||
| chr10:103305553 | G | T | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.997-1592C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305553 | |||||||
| chr10:103305610 | TAA | T | 4 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.997-1651_997-1650d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305610 | |||||||
| chr10:103305652 | C | T | 181 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(178): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.997-1691G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305652 | |||||||
| chr10:103305802 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.997-1841G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305802 | |||||||
| chr10:103305850 | C | A | 5 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02809.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.997-1889G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305850 | |||||||
| chr10:103305994 | T | G | 2 | a0002c0002t0001g0124 a0002c0002t0001g0167 |
2 | NA18954.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.997-2033A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103305994 | |||||||
| chr10:103306040 | T | G | 1 | a0002c0002t0001g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.997-2079A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306040 | |||||||
| chr10:103306088 | C | CA | 169 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(166): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.997-2128_997-2127i others(3): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306088 | |||||||
| chr10:103306102 | C | CT | 48 | a0002c0002t0001g0002 a0002c0002t0001g0014 a0002c0002t0001g0015 others(45): Show |
50 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.997-2142dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306102 | |||||||
| chr10:103306102 | CT | C | 9 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(6): Show |
9 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.997-2142delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306102 | |||||||
| chr10:103306260 | G | A | 1 | a0002c0002t0001g0095 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.997-2299C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306260 | |||||||
| chr10:103306557 | T | C | 35 | a0002c0002t0001g0002 a0002c0002t0001g0014 a0002c0002t0001g0015 others(32): Show |
37 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.997-2596A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306557 | |||||||
| chr10:103306564 | C | T | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.997-2603G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306564 | |||||||
| chr10:103306705 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.997-2744G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306705 | |||||||
| chr10:103306828 | G | A | 13 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(10): Show |
15 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.997-2867C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306828 | |||||||
| chr10:103306830 | G | T | 1 | a0002c0002t0001g0014 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.997-2869C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306830 | |||||||
| chr10:103306876 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.997-2915C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306876 | |||||||
| chr10:103306981 | A | G | 2 | a0002c0002t0002g0132 a0002c0002t0002g0133 |
2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.997-3020T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103306981 | |||||||
| chr10:103307190 | C | A | 3 | a0002c0002t0001g0109 a0002c0002t0001g0161 a0002c0002t0001g0162 |
3 | NA18959.hp2 NA18980.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.997-3229G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307190 | |||||||
| chr10:103307280 | T | C | 203 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(200): Show |
210 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.997-3319A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307280 | |||||||
| chr10:103307460 | G | C | 4 | a0002c0002t0001g0100 a0002c0002t0001g0114 a0002c0002t0001g0148 others(1): Show |
4 | NA18951.hp1 NA19012.hp2 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.997-3499C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307460 | |||||||
| chr10:103307465 | AAAGT | A | 4 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0033 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.997-3508_997-3505d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307465 | |||||||
| chr10:103307517 | C | T | 2 | a0002c0002t0001g0126 a0002c0002t0001g0165 |
2 | HG01167.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.997-3556G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307517 | |||||||
| chr10:103307847 | T | G | 1 | a0002c0002t0001g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.997-3886A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103307847 | |||||||
| chr10:103308078 | A | T | 1 | a0002c0002t0001g0068 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.997-4117T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308078 | |||||||
| chr10:103308098 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0298 |
2 | HG00609.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.997-4137T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308098 | |||||||
| chr10:103308169 | T | C | 1 | a0002c0002t0001g0148 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.997-4208A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308169 | |||||||
| chr10:103308462 | G | A | 2 | a0002c0002t0001g0117 a0002c0002t0001g0137 |
2 | HG02809.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.997-4501C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308462 | |||||||
| chr10:103308476 | G | A | 1 | a0002c0002t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.997-4515C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308476 | |||||||
| chr10:103308503 | A | G | 1 | a0002c0002t0001g0172 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.997-4542T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308503 | |||||||
| chr10:103308510 | T | C | 17 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(14): Show |
19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.997-4549A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308510 | |||||||
| chr10:103308568 | T | C | 3 | a0001c0001t0001g0257 a0001c0001t0001g0282 a0001c0001t0001g0283 |
3 | HG02818.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.997-4607A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308568 | |||||||
| chr10:103308660 | C | G | 6 | a0002c0002t0001g0058 a0002c0002t0001g0060 a0002c0002t0001g0061 others(3): Show |
6 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.997-4699G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103308660 | |||||||
| chr10:103309140 | G | T | 11 | a0002c0002t0001g0046 a0002c0002t0001g0050 a0002c0002t0001g0051 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.996+5046C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309140 | |||||||
| chr10:103309196 | T | TG | 53 | a0001c0001t0001g0178 a0001c0001t0001g0215 a0001c0001t0001g0241 others(50): Show |
55 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.996+4989dupC | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309196 | |||||||
| chr10:103309197 | G | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0244 a0001c0001t0001g0246 others(18): Show |
23 | HG01361.hp1 HG01928.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.996+4989C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309197 | |||||||
| chr10:103309363 | A | C | 169 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(166): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.996+4823T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309363 | |||||||
| chr10:103309482 | G | C | 12 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(9): Show |
14 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.996+4704C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309482 | |||||||
| chr10:103309775 | A | T | 1 | a0002c0002t0001g0032 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.996+4411T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309775 | |||||||
| chr10:103309954 | C | CT | 8 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 others(5): Show |
8 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.996+4231dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309954 | |||||||
| chr10:103309954 | C | CTT | 35 | a0002c0002t0001g0002 a0002c0002t0001g0014 a0002c0002t0001g0015 others(32): Show |
37 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.996+4230_996+4231d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309954 | |||||||
| chr10:103309954 | CT | C | 17 | a0001c0001t0001g0219 a0001c0001t0001g0286 a0001c0001t0001g0331 others(14): Show |
17 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.996+4231delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103309954 | |||||||
| chr10:103310116 | A | G | 7 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0219 others(4): Show |
7 | HG02622.hp1 HG02896.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.996+4070T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310116 | |||||||
| chr10:103310189 | T | C | 1 | a0002c0002t0001g0123 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.996+3997A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310189 | |||||||
| chr10:103310203 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.996+3983G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310203 | |||||||
| chr10:103310228 | A | C | 1 | a0002c0002t0001g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.996+3958T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310228 | |||||||
| chr10:103310229 | G | A | 4 | a0001c0001t0001g0259 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG01952.hp2 HG01981.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.996+3957C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310229 | |||||||
| chr10:103310496 | T | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0215 others(59): Show |
65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.996+3690A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310496 | |||||||
| chr10:103310630 | C | A | 1 | a0001c0001t0001g0279 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.996+3556G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310630 | |||||||
| chr10:103310903 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0242 a0001c0001t0001g0243 others(5): Show |
9 | HG00423.hp2 NA18612.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.996+3283C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103310903 | |||||||
| chr10:103311001 | A | T | 1 | a0001c0001t0001g0345 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.996+3185T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311001 | |||||||
| chr10:103311080 | C | T | 35 | a0002c0002t0001g0002 a0002c0002t0001g0014 a0002c0002t0001g0015 others(32): Show |
37 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.996+3106G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311080 | |||||||
| chr10:103311084 | T | A | 17 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(14): Show |
19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.996+3102A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311084 | |||||||
| chr10:103311205 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.996+2981C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311205 | |||||||
| chr10:103311325 | A | G | 2 | a0001c0001t0001g0183 a0001c0001t0001g0206 |
2 | HG00673.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.996+2861T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311325 | |||||||
| chr10:103311414 | T | C | 1 | a0002c0002t0001g0126 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.996+2772A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311414 | |||||||
| chr10:103311447 | C | CT | 6 | a0001c0001t0001g0243 a0001c0001t0001g0335 a0002c0002t0001g0014 others(3): Show |
6 | HG00544.hp1 HG00597.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.996+2738dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311447 | |||||||
| chr10:103311447 | CT | C | 11 | a0001c0001t0001g0229 a0001c0001t0001g0261 a0001c0001t0001g0310 others(8): Show |
11 | HG00438.hp1 HG00558.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.996+2738delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311447 | |||||||
| chr10:103311812 | C | G | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.996+2374G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103311812 | |||||||
| chr10:103312084 | C | CA | 174 | a0001c0001t0001g0175 a0001c0001t0001g0189 a0001c0001t0001g0191 others(171): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.996+2101dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312084 | |||||||
| chr10:103312084 | C | CAA | 30 | a0001c0001t0001g0210 a0001c0001t0001g0342 a0001c0001t0001g0343 others(27): Show |
30 | HG00621.hp1 HG01261.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.996+2100_996+2101d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312084 | |||||||
| chr10:103312253 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.996+1933G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312253 | |||||||
| chr10:103312272 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.996+1914T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312272 | |||||||
| chr10:103312561 | C | A | 1 | a0001c0001t0001g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.996+1625G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312561 | |||||||
| chr10:103312687 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.996+1499G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312687 | |||||||
| chr10:103312773 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.996+1413G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312773 | |||||||
| chr10:103312829 | C | T | 1 | a0002c0002t0001g0165 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.996+1357G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312829 | |||||||
| chr10:103312944 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.996+1242C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312944 | |||||||
| chr10:103312959 | T | TCAAAAA | 48 | a0001c0001t0001g0335 a0001c0001t0003g0009 a0001c0001t0003g0010 others(45): Show |
52 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.996+1221_996+1226d others(8): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312959 | |||||||
| chr10:103312959 | T | TCAAAAAC others(5): Show |
12 | a0002c0002t0001g0070 a0002c0002t0004g0016 a0002c0002t0004g0024 others(9): Show |
12 | HG00673.hp1 NA18943.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.996+1215_996+1226d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312959 | |||||||
| chr10:103312959 | T | TCAAAAAC others(11): Show |
1 | a0002c0002t0004g0030 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.996+1209_996+1226d others(20): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312959 | |||||||
| chr10:103312959 | TCAAAAA | T | 109 | a0001c0001t0001g0216 a0001c0001t0001g0237 a0001c0001t0001g0245 others(106): Show |
112 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.996+1221_996+1226d others(8): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312959 | |||||||
| chr10:103312959 | TCAAAAAC others(11): Show |
T | 1 | a0002c0002t0001g0159 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.996+1209_996+1226d others(20): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103312959 | |||||||
| chr10:103313047 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.996+1139G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313047 | |||||||
| chr10:103313154 | T | A | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.996+1032A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313154 | |||||||
| chr10:103313313 | C | T | 101 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0045 others(98): Show |
104 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.996+873G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313313 | |||||||
| chr10:103313495 | G | T | 12 | a0001c0001t0001g0183 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
12 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.996+691C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313495 | |||||||
| chr10:103313575 | A | T | 1 | a0001c0001t0001g0268 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.996+611T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313575 | |||||||
| chr10:103313617 | G | GA | 17 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(14): Show |
19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.996+568dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313617 | |||||||
| chr10:103313677 | G | A | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0190 |
3 | HG02559.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.996+509C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313677 | |||||||
| chr10:103313716 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.996+470A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313716 | |||||||
| chr10:103313858 | T | C | 1 | a0002c0002t0001g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.996+328A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 9/9 | chr10 | 103313858 | |||||||
| chr10:103314511 | T | G | 1 | a0002c0002t0001g0145 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.910-239A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314511 | |||||||
| chr10:103314574 | CATTA | C | 4 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-306_910-303del others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314574 | |||||||
| chr10:103314628 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.910-356T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314628 | |||||||
| chr10:103314797 | A | G | 4 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-525T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314797 | |||||||
| chr10:103314954 | T | TA | 123 | a0001c0001t0001g0004 a0001c0001t0001g0188 a0001c0001t0001g0189 others(120): Show |
129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.910-683dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314954 | |||||||
| chr10:103314954 | T | TAA | 59 | a0001c0001t0001g0186 a0001c0001t0001g0190 a0001c0001t0001g0265 others(56): Show |
62 | HG00544.hp2 HG00597.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.910-684_910-683dup others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314954 | |||||||
| chr10:103314954 | T | TAAA | 9 | a0001c0001t0001g0185 a0001c0001t0003g0204 a0001c0001t0003g0205 others(6): Show |
9 | HG01433.hp1 HG01433.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.910-685_910-683dup others(3): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314954 | |||||||
| chr10:103314954 | TA | T | 66 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(63): Show |
69 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.910-683delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314954 | |||||||
| chr10:103314955 | A | T | 1 | a0001c0001t0001g0345 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.910-683T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103314955 | |||||||
| chr10:103315093 | T | C | 12 | a0002c0002t0001g0164 a0002c0002t0004g0016 a0002c0002t0004g0024 others(9): Show |
12 | NA18943.hp2 NA18945.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.910-821A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315093 | |||||||
| chr10:103315261 | T | C | 2 | a0002c0002t0001g0171 a0002c0002t0001g0173 |
2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.910-989A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315261 | |||||||
| chr10:103315314 | T | C | 5 | a0002c0002t0001g0002 a0002c0002t0001g0034 a0002c0002t0001g0042 others(2): Show |
7 | HG00099.hp1 HG00280.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-1042A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315314 | |||||||
| chr10:103315318 | T | C | 3 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG02886.hp1 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.910-1046A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315318 | |||||||
| chr10:103315560 | T | C | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.910-1288A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315560 | |||||||
| chr10:103315585 | T | C | 11 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(8): Show |
11 | HG02258.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.910-1313A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315585 | |||||||
| chr10:103315718 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.910-1446C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315718 | |||||||
| chr10:103315955 | C | T | 100 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0045 others(97): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.910-1683G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315955 | |||||||
| chr10:103315968 | A | ATG | 7 | a0001c0001t0001g0234 a0001c0001t0001g0235 a0001c0001t0001g0236 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-1698_910-1697d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315968 | |||||||
| chr10:103315968 | ATG | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(24): Show |
29 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.910-1698_910-1697d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315968 | |||||||
| chr10:103315968 | ATGTG | A | 8 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(5): Show |
8 | HG01099.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.910-1700_910-1697d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315968 | |||||||
| chr10:103315981 | T | G | 23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(20): Show |
25 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.910-1709A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315981 | |||||||
| chr10:103315983 | T | G | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.910-1711A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315983 | |||||||
| chr10:103315990 | GTGTGTA | G | 5 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02809.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-1724_910-1719d others(8): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315990 | |||||||
| chr10:103315992 | G | A | 7 | a0001c0001t0001g0188 a0001c0001t0001g0219 a0001c0001t0001g0341 others(4): Show |
7 | HG02896.hp1 HG03041.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.910-1720C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315992 | |||||||
| chr10:103315992 | G | GTA | 5 | a0001c0001t0001g0228 a0001c0001t0003g0010 a0001c0001t0003g0193 others(2): Show |
5 | HG01081.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.910-1721_910-1720i others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315992 | |||||||
| chr10:103315994 | G | A | 71 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(68): Show |
77 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.910-1722C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315994 | |||||||
| chr10:103315994 | G | GTA | 4 | a0002c0002t0004g0016 a0002c0002t0004g0027 a0002c0002t0004g0030 others(1): Show |
4 | NA18940.hp1 NA18963.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-1724_910-1723d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315994 | |||||||
| chr10:103315994 | G | GTGTA | 4 | a0002c0002t0001g0014 a0002c0002t0001g0023 a0002c0002t0001g0070 others(1): Show |
4 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-1723_910-1722i others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315994 | |||||||
| chr10:103315994 | GTA | G | 61 | a0001c0001t0001g0238 a0001c0001t0001g0250 a0001c0001t0001g0294 others(58): Show |
62 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.910-1724_910-1723d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315994 | |||||||
| chr10:103315994 | GTATA | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0011 others(30): Show |
35 | HG00423.hp2 HG00609.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.910-1726_910-1723d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315994 | |||||||
| chr10:103315996 | A | G | 29 | a0001c0001t0001g0235 a0001c0001t0001g0285 a0001c0001t0001g0291 others(26): Show |
29 | HG00140.hp1 HG00323.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.910-1724T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315996 | |||||||
| chr10:103315997 | TATATATA others(13): Show |
T | 1 | a0001c0001t0001g0251 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.910-1745_910-1726d others(22): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315997 | |||||||
| chr10:103315998 | A | G | 7 | a0001c0001t0001g0250 a0001c0001t0001g0291 a0002c0002t0001g0017 others(4): Show |
7 | HG01884.hp1 HG02145.hp1 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.910-1726T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103315998 | |||||||
| chr10:103316000 | A | G | 5 | a0002c0002t0001g0058 a0002c0002t0001g0060 a0002c0002t0001g0061 others(2): Show |
5 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-1728T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316000 | |||||||
| chr10:103316009 | T | G | 6 | a0001c0001t0001g0177 a0001c0001t0001g0180 a0001c0001t0001g0182 others(3): Show |
6 | HG00733.hp2 HG00738.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.910-1737A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316009 | |||||||
| chr10:103316009 | TATATAGA others(7): Show |
T | 4 | a0001c0001t0001g0259 a0001c0001t0001g0304 a0001c0001t0001g0305 others(1): Show |
4 | HG01952.hp2 HG01981.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.910-1751_910-1738d others(16): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316009 | |||||||
| chr10:103316011 | T | G | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0177 others(22): Show |
27 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.910-1739A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316011 | |||||||
| chr10:103316011 | TATAG | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
53 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.910-1743_910-1740d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316011 | |||||||
| chr10:103316011 | TATAGAGA others(3): Show |
T | 1 | a0002c0002t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.910-1749_910-1740d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316011 | |||||||
| chr10:103316013 | T | G | 76 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(73): Show |
78 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.910-1741A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | |||||||
| chr10:103316013 | T | TAG | 3 | a0001c0001t0003g0010 a0001c0001t0003g0194 a0001c0001t0003g0201 |
3 | HG01074.hp1 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.910-1743_910-1742d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | |||||||
| chr10:103316013 | T | TAGAGAG | 3 | a0001c0001t0003g0009 a0001c0001t0003g0199 a0001c0001t0003g0204 |
3 | HG02717.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.910-1747_910-1742d others(8): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | |||||||
| chr10:103316013 | T | TATAG | 3 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0344 |
3 | HG03041.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.910-1742_910-1741i others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | |||||||
| chr10:103316013 | TAG | T | 21 | a0001c0001t0001g0285 a0001c0001t0001g0326 a0001c0001t0001g0332 others(18): Show |
22 | HG00323.hp1 HG00558.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.910-1743_910-1742d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | |||||||
| chr10:103316013 | TAGAG | T | 33 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0240 others(30): Show |
35 | HG00408.hp1 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.910-1745_910-1742d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | |||||||
| chr10:103316013 | TAGAGAGA others(5): Show |
T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.910-1753_910-1742d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316013 | |||||||
| chr10:103316015 | G | T | 53 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0207 others(50): Show |
55 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.910-1743C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316015 | |||||||
| chr10:103316017 | G | T | 31 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(28): Show |
33 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.910-1745C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316017 | |||||||
| chr10:103316019 | G | T | 19 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(16): Show |
19 | HG01175.hp1 HG01192.hp2 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.910-1747C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316019 | |||||||
| chr10:103316021 | G | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-1749C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316021 | |||||||
| chr10:103316023 | G | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0191 |
2 | HG02145.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.910-1751C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316023 | |||||||
| chr10:103316237 | T | C | 3 | a0002c0002t0002g0127 a0002c0002t0002g0128 a0002c0002t0002g0151 |
3 | HG00741.hp1 HG01071.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.910-1965A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316237 | |||||||
| chr10:103316567 | T | C | 1 | a0002c0002t0007g0085 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.910-2295A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316567 | |||||||
| chr10:103316626 | C | T | 12 | a0002c0002t0001g0002 a0002c0002t0001g0015 a0002c0002t0001g0032 others(9): Show |
14 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-2354G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316626 | |||||||
| chr10:103316967 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.910-2695A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103316967 | |||||||
| chr10:103317367 | C | A | 168 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(165): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.910-3095G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317367 | |||||||
| chr10:103317693 | T | C | 1 | a0002c0002t0001g0095 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.910-3421A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317693 | |||||||
| chr10:103317763 | G | GT | 13 | a0001c0001t0001g0228 a0002c0002t0001g0058 a0002c0002t0001g0059 others(10): Show |
13 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.910-3492dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317763 | |||||||
| chr10:103317764 | T | A | 1 | a0001c0001t0001g0315 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.910-3492A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317764 | |||||||
| chr10:103317787 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.910-3515C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317787 | |||||||
| chr10:103317886 | G | A | 1 | a0002c0002t0001g0056 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.910-3614C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103317886 | |||||||
| chr10:103318038 | T | C | 1 | a0002c0002t0001g0095 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.910-3766A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318038 | |||||||
| chr10:103318046 | C | T | 2 | a0002c0002t0001g0107 a0002c0002t0001g0169 |
2 | HG02056.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.910-3774G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318046 | |||||||
| chr10:103318209 | G | A | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.910-3937C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318209 | |||||||
| chr10:103318212 | A | G | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.910-3940T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318212 | |||||||
| chr10:103318213 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.910-3941G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318213 | |||||||
| chr10:103318218 | A | G | 2 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
2 | HG00408.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.910-3946T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318218 | |||||||
| chr10:103318398 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.910-4126C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318398 | |||||||
| chr10:103318466 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.910-4194G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318466 | |||||||
| chr10:103318472 | C | T | 1 | a0002c0002t0002g0131 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.910-4200G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318472 | |||||||
| chr10:103318692 | T | C | 1 | a0002c0002t0001g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.910-4420A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318692 | |||||||
| chr10:103318707 | G | A | 1 | a0002c0002t0001g0068 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.910-4435C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318707 | |||||||
| chr10:103318775 | G | C | 4 | a0002c0002t0004g0025 a0002c0002t0004g0029 a0002c0002t0004g0036 others(1): Show |
4 | NA18971.hp1 NA18982.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.910-4503C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318775 | |||||||
| chr10:103318868 | C | T | 5 | a0002c0002t0001g0015 a0002c0002t0001g0032 a0002c0002t0001g0037 others(2): Show |
5 | HG00639.hp1 HG00738.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.910-4596G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318868 | |||||||
| chr10:103318944 | T | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0206 |
2 | HG00673.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.910-4672A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103318944 | |||||||
| chr10:103319036 | T | C | 24 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(21): Show |
26 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.910-4764A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319036 | |||||||
| chr10:103319373 | G | A | 12 | a0002c0002t0001g0002 a0002c0002t0001g0015 a0002c0002t0001g0032 others(9): Show |
14 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.910-5101C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319373 | |||||||
| chr10:103319402 | C | T | 1 | a0002c0002t0001g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.910-5130G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319402 | |||||||
| chr10:103319405 | C | T | 168 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(165): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.910-5133G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319405 | |||||||
| chr10:103319660 | T | C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0215 others(59): Show |
65 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.910-5388A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319660 | |||||||
| chr10:103319682 | T | C | 168 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(165): Show |
175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.910-5410A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319682 | |||||||
| chr10:103319855 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.910-5583A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319855 | |||||||
| chr10:103319979 | T | C | 1 | a0002c0002t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.910-5707A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103319979 | |||||||
| chr10:103320262 | A | G | 3 | a0002c0002t0001g0097 a0002c0002t0001g0102 a0002c0002t0001g0103 |
3 | NA19055.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.910-5990T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320262 | |||||||
| chr10:103320358 | A | G | 1 | a0002c0002t0002g0163 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.910-6086T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320358 | |||||||
| chr10:103320555 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.909+5979G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320555 | |||||||
| chr10:103320624 | T | C | 17 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(14): Show |
19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.909+5910A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320624 | |||||||
| chr10:103320690 | C | CA | 11 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(8): Show |
11 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.909+5843dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320690 | |||||||
| chr10:103320745 | T | G | 2 | a0002c0002t0001g0062 a0002c0002t0001g0063 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.909+5789A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320745 | |||||||
| chr10:103320748 | G | C | 1 | a0002c0002t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.909+5786C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320748 | |||||||
| chr10:103320818 | T | C | 227 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(224): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.909+5716A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320818 | |||||||
| chr10:103320930 | T | A | 4 | a0002c0002t0004g0025 a0002c0002t0004g0029 a0002c0002t0004g0036 others(1): Show |
4 | NA18971.hp1 NA18982.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+5604A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103320930 | |||||||
| chr10:103321348 | A | G | 12 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0060 others(9): Show |
12 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.909+5186T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103321348 | |||||||
| chr10:103321670 | C | T | 1 | a0001c0001t0001g0340 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.909+4864G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103321670 | |||||||
| chr10:103322148 | G | T | 1 | a0002c0002t0001g0129 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.909+4386C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322148 | |||||||
| chr10:103322174 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.909+4360C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322174 | |||||||
| chr10:103322175 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.909+4359C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322175 | |||||||
| chr10:103322349 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.909+4185C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322349 | |||||||
| chr10:103322426 | A | G | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+4108T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322426 | |||||||
| chr10:103322784 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.909+3750T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322784 | |||||||
| chr10:103322822 | T | TCA | 3 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0005g0012 |
3 | HG02109.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.909+3710_909+3711d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322822 | |||||||
| chr10:103322878 | C | CA | 20 | a0001c0001t0001g0330 a0001c0001t0001g0337 a0001c0001t0003g0009 others(17): Show |
22 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.909+3655dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322878 | |||||||
| chr10:103322900 | A | C | 4 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+3634T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322900 | |||||||
| chr10:103322903 | C | A | 9 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(6): Show |
9 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.909+3631G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322903 | |||||||
| chr10:103322904 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.909+3630T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103322904 | |||||||
| chr10:103323114 | A | G | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+3420T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323114 | |||||||
| chr10:103323175 | T | C | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+3359A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323175 | |||||||
| chr10:103323225 | A | T | 1 | a0001c0001t0001g0242 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.909+3309T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323225 | |||||||
| chr10:103323249 | T | C | 1 | a0002c0002t0001g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.909+3285A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323249 | |||||||
| chr10:103323422 | A | C | 1 | a0002c0002t0001g0095 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.909+3112T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323422 | |||||||
| chr10:103323422 | A | G | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+3112T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323422 | |||||||
| chr10:103323469 | T | C | 3 | a0001c0001t0001g0266 a0001c0001t0001g0269 a0001c0001t0001g0294 |
3 | HG02129.hp2 NA18939.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.909+3065A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323469 | |||||||
| chr10:103323531 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.909+3003C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323531 | |||||||
| chr10:103323614 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.909+2920A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323614 | |||||||
| chr10:103323660 | T | C | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+2874A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103323660 | |||||||
| chr10:103324130 | G | T | 2 | a0001c0001t0001g0306 a0001c0001t0001g0317 |
2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.909+2404C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324130 | |||||||
| chr10:103324146 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.909+2388G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324146 | |||||||
| chr10:103324328 | GA | G | 150 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0006 others(147): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.909+2205delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324328 | |||||||
| chr10:103324328 | GAA | G | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(22): Show |
27 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.909+2204_909+2205d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324328 | |||||||
| chr10:103324329 | A | AAAAAAAA others(316): Show |
2 | a0001c0001t0003g0202 a0001c0001t0003g0204 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.909+2204_909+2205i others(325): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324329 | |||||||
| chr10:103324329 | A | AAAAAAAA others(315): Show |
13 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(10): Show |
14 | HG01074.hp1 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.909+2204_909+2205i others(324): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324329 | |||||||
| chr10:103324329 | A | AAAAAAAA others(314): Show |
2 | a0001c0001t0003g0010 a0001c0001t0003g0195 |
2 | HG01081.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.909+2204_909+2205i others(323): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324329 | |||||||
| chr10:103324330 | A | AAAAAAAA others(314): Show |
1 | a0003c0005t0003g0355 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.909+2203_909+2204i others(323): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324330 | |||||||
| chr10:103324450 | C | T | 11 | a0002c0002t0001g0046 a0002c0002t0001g0050 a0002c0002t0001g0051 others(8): Show |
11 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.909+2084G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324450 | |||||||
| chr10:103324535 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.909+1999C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324535 | |||||||
| chr10:103324562 | G | C | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+1972C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324562 | |||||||
| chr10:103324599 | A | T | 1 | a0001c0001t0001g0208 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.909+1935T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324599 | |||||||
| chr10:103324637 | G | A | 12 | a0001c0001t0001g0183 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
12 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.909+1897C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324637 | |||||||
| chr10:103324685 | G | A | 1 | a0002c0002t0001g0153 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.909+1849C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324685 | |||||||
| chr10:103324692 | G | A | 5 | a0002c0002t0002g0127 a0002c0002t0002g0128 a0002c0002t0002g0130 others(2): Show |
5 | HG00741.hp1 HG00741.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+1842C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324692 | |||||||
| chr10:103324759 | C | CA | 20 | a0001c0001t0001g0213 a0001c0001t0001g0241 a0001c0001t0001g0244 others(17): Show |
20 | HG00597.hp1 HG00597.hp2 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.909+1774dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324759 | |||||||
| chr10:103324759 | CA | C | 8 | a0002c0002t0001g0046 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+1774delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324759 | |||||||
| chr10:103324774 | C | A | 1 | a0002c0002t0004g0024 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.909+1760G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324774 | |||||||
| chr10:103324775 | C | A | 1 | a0001c0001t0001g0243 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.909+1759G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324775 | |||||||
| chr10:103324775 | C | CA | 25 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0003g0009 others(22): Show |
27 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.909+1758dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324775 | |||||||
| chr10:103324776 | A | C | 1 | a0002c0002t0004g0024 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.909+1758T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324776 | |||||||
| chr10:103324812 | C | T | 3 | a0002c0002t0001g0129 a0002c0002t0001g0146 a0002c0002t0007g0085 |
3 | NA18955.hp2 NA19011.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.909+1722G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324812 | |||||||
| chr10:103324891 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.909+1643A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103324891 | |||||||
| chr10:103325043 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.909+1491C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325043 | |||||||
| chr10:103325050 | G | A | 8 | a0002c0002t0001g0014 a0002c0002t0001g0021 a0002c0002t0001g0022 others(5): Show |
8 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1484C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325050 | |||||||
| chr10:103325060 | G | A | 8 | a0002c0002t0001g0046 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+1474C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325060 | |||||||
| chr10:103325067 | G | A | 7 | a0002c0002t0001g0006 a0002c0002t0001g0095 a0002c0002t0001g0096 others(4): Show |
8 | HG01934.hp1 HG02273.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+1467C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325067 | |||||||
| chr10:103325083 | C | T | 151 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0006 others(148): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.909+1451G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325083 | |||||||
| chr10:103325124 | G | C | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02886.hp1 HG03041.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+1410C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325124 | |||||||
| chr10:103325142 | T | TAAATA | 48 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(45): Show |
50 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.909+1387_909+1391d others(7): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325142 | |||||||
| chr10:103325142 | T | TAAATAAA others(3): Show |
23 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(20): Show |
25 | HG01074.hp1 HG01081.hp1 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.909+1382_909+1391d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325142 | |||||||
| chr10:103325142 | T | TAAATAAA others(8): Show |
1 | a0001c0001t0003g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.909+1377_909+1391d others(17): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325142 | |||||||
| chr10:103325142 | TAAATA | T | 148 | a0001c0001t0001g0218 a0002c0002t0001g0002 a0002c0002t0001g0003 others(145): Show |
153 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.909+1387_909+1391d others(7): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325142 | |||||||
| chr10:103325142 | TAAATAAA others(3): Show |
T | 3 | a0002c0002t0001g0019 a0002c0002t0001g0058 a0002c0002t0001g0065 |
3 | HG01109.hp2 HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.909+1382_909+1391d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325142 | |||||||
| chr10:103325277 | G | A | 1 | a0002c0002t0001g0149 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.909+1257C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325277 | |||||||
| chr10:103325414 | C | T | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+1120G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325414 | |||||||
| chr10:103325434 | T | C | 52 | a0002c0002t0001g0073 a0002c0002t0001g0076 a0002c0002t0001g0078 others(49): Show |
52 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.909+1100A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325434 | |||||||
| chr10:103325493 | C | A | 1 | a0002c0002t0001g0162 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.909+1041G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325493 | |||||||
| chr10:103325539 | C | T | 17 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(14): Show |
19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.909+995G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325539 | |||||||
| chr10:103325605 | C | T | 3 | a0002c0002t0001g0097 a0002c0002t0001g0102 a0002c0002t0001g0103 |
3 | NA19055.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.909+929G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325605 | |||||||
| chr10:103325852 | T | TA | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(48): Show |
53 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.909+681dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325852 | |||||||
| chr10:103325852 | TA | T | 8 | a0001c0001t0001g0228 a0001c0001t0001g0236 a0001c0001t0001g0261 others(5): Show |
8 | HG01070.hp1 HG02895.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.909+681delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325852 | |||||||
| chr10:103325852 | TAA | T | 160 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(157): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.909+680_909+681del others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325852 | |||||||
| chr10:103325852 | TAAA | T | 7 | a0002c0002t0001g0092 a0002c0002t0001g0097 a0002c0002t0001g0104 others(4): Show |
7 | HG00733.hp1 HG01433.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.909+679_909+681del others(3): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103325852 | |||||||
| chr10:103326018 | A | C | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+516T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326018 | |||||||
| chr10:103326022 | CCT | C | 8 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
8 | HG02071.hp2 HG02074.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.909+510_909+511del others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326022 | |||||||
| chr10:103326198 | CCA | C | 17 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(14): Show |
19 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.909+334_909+335del others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326198 | |||||||
| chr10:103326302 | T | A | 5 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02809.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.909+232A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326302 | |||||||
| chr10:103326305 | C | T | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.909+229G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326305 | |||||||
| chr10:103326385 | T | C | 4 | a0001c0001t0001g0315 a0001c0001t0001g0324 a0001c0001t0001g0336 others(1): Show |
4 | HG01361.hp1 HG01934.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.909+149A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326385 | |||||||
| chr10:103326388 | C | CA | 35 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(32): Show |
37 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(34): Show |
intron_variant | MODIFIER | c.909+145dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326388 | |||||||
| chr10:103326436 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.909+98T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 8/9 | chr10 | 103326436 | |||||||
| chr10:103326655 | C | T | 10 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(7): Show |
10 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.811-23G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103326655 | |||||||
| chr10:103326776 | T | C | 1 | a0002c0002t0001g0173 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.811-144A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103326776 | |||||||
| chr10:103326953 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.811-321G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103326953 | |||||||
| chr10:103327129 | A | G | 11 | a0002c0002t0004g0016 a0002c0002t0004g0024 a0002c0002t0004g0025 others(8): Show |
11 | NA18943.hp2 NA18945.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.811-497T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327129 | |||||||
| chr10:103327204 | G | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0301 |
2 | HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.811-572C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327204 | |||||||
| chr10:103327246 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.811-614A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327246 | |||||||
| chr10:103327354 | G | T | 1 | a0002c0002t0001g0114 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.811-722C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327354 | |||||||
| chr10:103327545 | T | G | 1 | a0002c0002t0001g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.811-913A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327545 | |||||||
| chr10:103327625 | C | T | 4 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-993G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327625 | |||||||
| chr10:103327799 | C | T | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.811-1167G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327799 | |||||||
| chr10:103327825 | C | G | 12 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0060 others(9): Show |
12 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.811-1193G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327825 | |||||||
| chr10:103327841 | A | AT | 12 | a0002c0002t0001g0002 a0002c0002t0001g0017 a0002c0002t0001g0018 others(9): Show |
14 | HG00099.hp1 HG00280.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.811-1210dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327841 | |||||||
| chr10:103327841 | AT | A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(37): Show |
42 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.811-1210delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327841 | |||||||
| chr10:103327910 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.811-1278G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327910 | |||||||
| chr10:103327922 | G | A | 8 | a0002c0002t0001g0046 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-1290C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103327922 | |||||||
| chr10:103328035 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.811-1403A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328035 | |||||||
| chr10:103328183 | C | T | 1 | a0002c0002t0001g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.811-1551G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328183 | |||||||
| chr10:103328235 | A | G | 1 | a0002c0002t0001g0119 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.811-1603T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328235 | |||||||
| chr10:103328354 | A | G | 1 | a0002c0002t0001g0145 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.811-1722T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328354 | |||||||
| chr10:103328536 | T | A | 1 | a0001c0001t0001g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.811-1904A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328536 | |||||||
| chr10:103328714 | T | C | 2 | a0001c0001t0001g0306 a0001c0001t0001g0317 |
2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.811-2082A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328714 | |||||||
| chr10:103328855 | G | T | 7 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0219 others(4): Show |
7 | HG02622.hp1 HG02896.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.811-2223C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328855 | |||||||
| chr10:103328879 | G | A | 1 | a0002c0002t0001g0056 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.811-2247C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328879 | |||||||
| chr10:103328947 | G | A | 1 | a0002c0002t0001g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.811-2315C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328947 | |||||||
| chr10:103328994 | C | A | 1 | a0001c0001t0003g0201 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.811-2362G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103328994 | |||||||
| chr10:103329150 | C | T | 2 | a0002c0002t0002g0132 a0002c0002t0002g0133 |
2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.811-2518G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329150 | |||||||
| chr10:103329166 | A | G | 8 | a0002c0002t0001g0046 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-2534T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329166 | |||||||
| chr10:103329189 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.811-2557C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329189 | |||||||
| chr10:103329204 | C | T | 3 | a0002c0002t0004g0027 a0002c0002t0004g0030 a0002c0002t0004g0039 |
3 | NA18940.hp1 NA18977.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.811-2572G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329204 | |||||||
| chr10:103329222 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.811-2590A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329222 | |||||||
| chr10:103329260 | A | G | 1 | a0001c0001t0001g0340 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.811-2628T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329260 | |||||||
| chr10:103329334 | C | A | 8 | a0002c0002t0001g0046 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-2702G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329334 | |||||||
| chr10:103329335 | C | A | 8 | a0002c0002t0001g0046 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.811-2703G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329335 | |||||||
| chr10:103329446 | C | T | 4 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.811-2814G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329446 | |||||||
| chr10:103329541 | G | A | 5 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG01891.hp2 HG02572.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.811-2909C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329541 | |||||||
| chr10:103329661 | C | T | 3 | a0002c0002t0001g0097 a0002c0002t0001g0102 a0002c0002t0001g0103 |
3 | NA19055.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.811-3029G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329661 | |||||||
| chr10:103329736 | G | A | 2 | a0002c0002t0001g0045 a0002c0002t0001g0055 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.811-3104C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329736 | |||||||
| chr10:103329741 | G | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.811-3109C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329741 | |||||||
| chr10:103329769 | G | A | 2 | a0001c0001t0001g0306 a0001c0001t0001g0317 |
2 | NA18975.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.811-3137C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329769 | |||||||
| chr10:103329771 | C | T | 3 | a0002c0002t0001g0097 a0002c0002t0001g0102 a0002c0002t0001g0103 |
3 | NA19055.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.811-3139G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329771 | |||||||
| chr10:103329990 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.811-3358G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103329990 | |||||||
| chr10:103330135 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.811-3503G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330135 | |||||||
| chr10:103330487 | T | TA | 9 | a0001c0001t0003g0202 a0002c0002t0001g0014 a0002c0002t0001g0021 others(6): Show |
9 | HG00544.hp1 HG00597.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.810+3437dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330487 | |||||||
| chr10:103330733 | G | A | 1 | a0001c0001t0001g0338 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.810+3192C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330733 | |||||||
| chr10:103330757 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.810+3168C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330757 | |||||||
| chr10:103330823 | G | T | 1 | a0002c0002t0002g0106 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.810+3102C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330823 | |||||||
| chr10:103330825 | A | G | 1 | a0002c0002t0001g0105 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.810+3100T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330825 | |||||||
| chr10:103330948 | C | T | 1 | a0002c0002t0001g0080 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.810+2977G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103330948 | |||||||
| chr10:103331242 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.810+2683C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331242 | |||||||
| chr10:103331446 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.810+2479A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331446 | |||||||
| chr10:103331616 | A | T | 9 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(6): Show |
9 | HG02071.hp2 HG02074.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.810+2309T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331616 | |||||||
| chr10:103331631 | T | A | 9 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(6): Show |
9 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.810+2294A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331631 | |||||||
| chr10:103331645 | G | A | 10 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0220 others(7): Show |
10 | HG02145.hp2 HG02257.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.810+2280C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331645 | |||||||
| chr10:103331702 | A | C | 51 | a0002c0002t0001g0073 a0002c0002t0001g0076 a0002c0002t0001g0082 others(48): Show |
51 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.810+2223T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103331702 | |||||||
| chr10:103332216 | G | T | 13 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(10): Show |
15 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.810+1709C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332216 | |||||||
| chr10:103332337 | T | C | 1 | a0002c0002t0001g0149 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.810+1588A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332337 | |||||||
| chr10:103332542 | C | A | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.810+1383G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332542 | |||||||
| chr10:103332579 | T | C | 4 | a0001c0001t0001g0248 a0001c0001t0001g0326 a0001c0001t0001g0333 others(1): Show |
4 | HG00558.hp2 HG02027.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.810+1346A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332579 | |||||||
| chr10:103332690 | T | C | 227 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(224): Show |
236 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.810+1235A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332690 | |||||||
| chr10:103332704 | T | C | 1 | a0002c0002t0001g0072 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.810+1221A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332704 | |||||||
| chr10:103332854 | C | G | 1 | a0002c0002t0001g0061 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.810+1071G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332854 | |||||||
| chr10:103332975 | G | A | 2 | a0001c0001t0003g0196 a0001c0001t0003g0197 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.810+950C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103332975 | |||||||
| chr10:103333032 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.810+893A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333032 | |||||||
| chr10:103333117 | T | TA | 23 | a0001c0001t0001g0226 a0001c0001t0001g0243 a0001c0001t0001g0345 others(20): Show |
25 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.810+807dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333117 | |||||||
| chr10:103333117 | TA | T | 77 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(74): Show |
84 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.810+807delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333117 | |||||||
| chr10:103333557 | T | C | 1 | a0001c0001t0001g0329 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.810+368A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333557 | |||||||
| chr10:103333814 | C | T | 1 | a0001c0001t0001g0335 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.810+111G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333814 | |||||||
| chr10:103333834 | T | A | 1 | a0002c0002t0001g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.810+91A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 7/9 | chr10 | 103333834 | |||||||
| chr10:103334261 | G | T | 3 | a0002c0002t0001g0097 a0002c0002t0001g0102 a0002c0002t0001g0103 |
3 | NA19055.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.783-309C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103334261 | |||||||
| chr10:103334642 | T | G | 2 | a0002c0002t0001g0045 a0002c0002t0001g0055 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.783-690A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103334642 | |||||||
| chr10:103334646 | G | C | 1 | a0001c0001t0001g0352 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.783-694C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103334646 | |||||||
| chr10:103335091 | T | A | 3 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0005g0012 |
3 | HG02109.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.783-1139A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335091 | |||||||
| chr10:103335216 | T | TA | 14 | a0001c0001t0001g0183 a0001c0001t0001g0206 a0001c0001t0001g0207 others(11): Show |
14 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.783-1265dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335216 | |||||||
| chr10:103335216 | TA | T | 6 | a0001c0001t0001g0229 a0001c0001t0001g0301 a0001c0001t0001g0341 others(3): Show |
6 | HG01070.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.783-1265delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335216 | |||||||
| chr10:103335366 | A | AT | 6 | a0001c0001t0001g0207 a0001c0001t0001g0310 a0001c0001t0001g0346 others(3): Show |
6 | HG00609.hp1 HG01192.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.783-1415dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335366 | |||||||
| chr10:103335423 | G | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0309 a0002c0002t0001g0015 |
3 | HG00099.hp2 HG01175.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.783-1471C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335423 | |||||||
| chr10:103335447 | T | C | 169 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(166): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.783-1495A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335447 | |||||||
| chr10:103335488 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.783-1536C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335488 | |||||||
| chr10:103335709 | T | C | 8 | a0002c0002t0001g0046 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.783-1757A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335709 | |||||||
| chr10:103335827 | T | C | 169 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(166): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.783-1875A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335827 | |||||||
| chr10:103335892 | G | A | 2 | a0002c0002t0001g0091 a0002c0002t0001g0118 |
2 | HG02738.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.783-1940C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335892 | |||||||
| chr10:103335941 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0239 others(51): Show |
59 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.783-1989G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335941 | |||||||
| chr10:103335952 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.783-2000G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103335952 | |||||||
| chr10:103336229 | G | A | 1 | a0002c0002t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.783-2277C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336229 | |||||||
| chr10:103336245 | T | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.783-2293A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336245 | |||||||
| chr10:103336247 | T | A | 1 | a0002c0002t0001g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.783-2295A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336247 | |||||||
| chr10:103336248 | A | T | 8 | a0001c0001t0001g0250 a0002c0002t0001g0058 a0002c0002t0001g0060 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.783-2296T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336248 | |||||||
| chr10:103336264 | A | G | 101 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0045 others(98): Show |
104 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.783-2312T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336264 | |||||||
| chr10:103336806 | C | T | 15 | a0002c0002t0004g0016 a0002c0002t0004g0020 a0002c0002t0004g0024 others(12): Show |
15 | HG00423.hp1 NA18940.hp1 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.783-2854G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336806 | |||||||
| chr10:103336970 | G | C | 1 | a0002c0002t0001g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.783-3018C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103336970 | |||||||
| chr10:103337274 | C | G | 1 | a0002c0002t0001g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.783-3322G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337274 | |||||||
| chr10:103337428 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.783-3476G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337428 | |||||||
| chr10:103337608 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.783-3656A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337608 | |||||||
| chr10:103337638 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.783-3686C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337638 | |||||||
| chr10:103337765 | TAAAAATA others(307): Show |
T | 169 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(166): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.783-4127_783-3814d others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337765 | |||||||
| chr10:103337831 | G | A | 12 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0060 others(9): Show |
12 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.783-3879C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103337831 | |||||||
| chr10:103338063 | CA | C | 94 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
98 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.783-4112delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338063 | |||||||
| chr10:103338063 | CAA | C | 5 | a0001c0001t0001g0011 a0001c0001t0001g0243 a0001c0001t0001g0249 others(2): Show |
6 | NA18612.hp2 NA18951.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.783-4113_783-4112d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338063 | |||||||
| chr10:103338134 | G | A | 1 | a0002c0002t0001g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.783-4182C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338134 | |||||||
| chr10:103338155 | T | C | 1 | a0002c0002t0001g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.783-4203A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338155 | |||||||
| chr10:103338267 | G | A | 98 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0072 others(95): Show |
101 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.783-4315C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338267 | |||||||
| chr10:103338277 | C | T | 2 | a0001c0001t0003g0009 a0001c0001t0003g0199 |
3 | HG02280.hp1 HG02717.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.783-4325G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338277 | |||||||
| chr10:103338380 | A | T | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.783-4428T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338380 | |||||||
| chr10:103338384 | A | G | 1 | a0002c0002t0001g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.783-4432T>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338384 | |||||||
| chr10:103338401 | C | A | 1 | a0001c0001t0003g0198 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.783-4449G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338401 | |||||||
| chr10:103338402 | G | A | 4 | a0002c0002t0001g0058 a0002c0002t0001g0061 a0002c0002t0001g0065 others(1): Show |
4 | HG01109.hp2 HG02055.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.783-4450C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338402 | |||||||
| chr10:103338470 | G | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.783-4518C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338470 | |||||||
| chr10:103338544 | C | CA | 92 | a0001c0001t0001g0271 a0002c0002t0001g0003 a0002c0002t0001g0045 others(89): Show |
94 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.783-4593dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338544 | |||||||
| chr10:103338544 | C | CAA | 9 | a0002c0002t0001g0006 a0002c0002t0001g0088 a0002c0002t0001g0095 others(6): Show |
10 | HG01934.hp1 HG02071.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.783-4594_783-4593d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338544 | |||||||
| chr10:103338664 | C | T | 1 | a0002c0002t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.783-4712G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338664 | |||||||
| chr10:103338725 | G | A | 1 | a0001c0001t0003g0198 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.783-4773C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338725 | |||||||
| chr10:103338740 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.783-4788G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338740 | |||||||
| chr10:103338741 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.783-4789C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103338741 | |||||||
| chr10:103339054 | A | T | 1 | a0002c0002t0001g0023 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.783-5102T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339054 | |||||||
| chr10:103339185 | C | T | 1 | a0001c0001t0001g0319 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.783-5233G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339185 | |||||||
| chr10:103339431 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.783-5479G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339431 | |||||||
| chr10:103339733 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+5291C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339733 | |||||||
| chr10:103339752 | G | A | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+5272C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339752 | |||||||
| chr10:103339766 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.782+5258G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339766 | |||||||
| chr10:103339801 | C | CA | 15 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0180 others(12): Show |
15 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.782+5222dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339801 | |||||||
| chr10:103339805 | AAAAAAAC others(6): Show |
A | 1 | a0002c0002t0001g0087 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.782+5206_782+5218d others(15): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339805 | |||||||
| chr10:103339806 | AAAAAACA others(3): Show |
A | 8 | a0001c0001t0001g0256 a0002c0002t0001g0050 a0002c0002t0001g0078 others(5): Show |
8 | HG01071.hp1 HG01167.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+5208_782+5217d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339806 | |||||||
| chr10:103339806 | AAAAAACA others(5): Show |
A | 17 | a0002c0002t0001g0003 a0002c0002t0001g0046 a0002c0002t0001g0082 others(14): Show |
19 | HG00544.hp2 HG01978.hp2 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.782+5206_782+5217d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339806 | |||||||
| chr10:103339806 | AAAAAACA others(7): Show |
A | 38 | a0002c0002t0001g0006 a0002c0002t0001g0052 a0002c0002t0001g0053 others(35): Show |
39 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(36): Show |
intron_variant | MODIFIER | c.782+5204_782+5217d others(16): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339806 | |||||||
| chr10:103339806 | AAAAAACA others(9): Show |
A | 9 | a0002c0002t0001g0051 a0002c0002t0001g0091 a0002c0002t0001g0144 others(6): Show |
9 | HG00140.hp1 HG02738.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.782+5202_782+5217d others(18): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339806 | |||||||
| chr10:103339806 | AAAAAACA others(13): Show |
A | 4 | a0002c0002t0004g0025 a0002c0002t0004g0029 a0002c0002t0004g0036 others(1): Show |
4 | NA18971.hp1 NA18982.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.782+5198_782+5217d others(22): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339806 | |||||||
| chr10:103339807 | AAAAACAC others(4): Show |
A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0257 a0001c0001t0001g0275 others(5): Show |
8 | HG00140.hp2 HG01361.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.782+5206_782+5216d others(13): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339807 | |||||||
| chr10:103339807 | AAAAACAC others(6): Show |
A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0300 a0001c0001t0001g0302 |
3 | HG01074.hp2 NA19077.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.782+5204_782+5216d others(15): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339807 | |||||||
| chr10:103339807 | AAAAACAC others(14): Show |
A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0263 a0001c0001t0001g0298 others(1): Show |
4 | HG00609.hp2 NA18747.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.782+5196_782+5216d others(23): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339807 | |||||||
| chr10:103339808 | AAAACACA others(1): Show |
A | 10 | a0001c0001t0003g0202 a0002c0002t0001g0017 a0002c0002t0001g0018 others(7): Show |
10 | HG00099.hp1 HG01109.hp1 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.782+5208_782+5215d others(10): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339808 | |||||||
| chr10:103339808 | AAAACACA others(3): Show |
A | 19 | a0002c0002t0001g0002 a0002c0002t0001g0037 a0002c0002t0001g0040 others(16): Show |
21 | HG00280.hp1 HG00280.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.782+5206_782+5215d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339808 | |||||||
| chr10:103339808 | AAAACACA others(5): Show |
A | 25 | a0001c0001t0001g0345 a0001c0001t0003g0010 a0002c0002t0001g0073 others(22): Show |
25 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.782+5204_782+5215d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339808 | |||||||
| chr10:103339808 | AAAACACA others(7): Show |
A | 6 | a0002c0002t0002g0079 a0002c0002t0002g0132 a0002c0002t0002g0133 others(3): Show |
6 | HG00323.hp2 HG00733.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.782+5202_782+5215d others(16): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339808 | |||||||
| chr10:103339808 | AAAACACA others(9): Show |
A | 1 | a0002c0002t0001g0122 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.782+5200_782+5215d others(18): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339808 | |||||||
| chr10:103339809 | AAACACAC | A | 16 | a0001c0001t0001g0186 a0001c0001t0001g0239 a0001c0001t0001g0241 others(13): Show |
16 | HG01981.hp2 HG02040.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.782+5208_782+5214d others(9): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339809 | |||||||
| chr10:103339809 | AAACACAC others(2): Show |
A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0258 a0001c0001t0001g0261 others(6): Show |
9 | HG01070.hp1 HG01175.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.782+5206_782+5214d others(11): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339809 | |||||||
| chr10:103339809 | AAACACAC others(4): Show |
A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0267 others(2): Show |
6 | HG01516.hp1 HG01928.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.782+5204_782+5214d others(13): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339809 | |||||||
| chr10:103339810 | A | C | 3 | a0001c0001t0001g0303 a0002c0002t0001g0075 a0002c0002t0001g0162 |
3 | HG00544.hp1 NA19003.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.782+5214T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | |||||||
| chr10:103339810 | AAC | A | 15 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0191 others(12): Show |
15 | HG00323.hp1 HG00673.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.782+5212_782+5213d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | |||||||
| chr10:103339810 | AACAC | A | 6 | a0001c0001t0001g0225 a0001c0001t0001g0255 a0001c0001t0001g0304 others(3): Show |
6 | HG01106.hp2 HG01981.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.782+5210_782+5213d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | |||||||
| chr10:103339810 | AACACAC | A | 11 | a0001c0001t0001g0224 a0001c0001t0001g0226 a0001c0001t0001g0238 others(8): Show |
11 | HG00597.hp2 HG01952.hp2 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.782+5208_782+5213d others(8): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | |||||||
| chr10:103339810 | AACACACA others(1): Show |
A | 10 | a0001c0001t0001g0237 a0001c0001t0001g0305 a0001c0001t0001g0312 others(7): Show |
11 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(8): Show |
intron_variant | MODIFIER | c.782+5206_782+5213d others(10): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | |||||||
| chr10:103339810 | AACACACA others(3): Show |
A | 3 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0003g0199 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.782+5204_782+5213d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | |||||||
| chr10:103339810 | AACACACA others(5): Show |
A | 12 | a0001c0001t0003g0010 a0001c0001t0003g0192 a0001c0001t0003g0193 others(9): Show |
12 | HG01074.hp1 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.782+5202_782+5213d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | |||||||
| chr10:103339810 | AACACACA others(9): Show |
A | 2 | a0001c0001t0001g0250 a0001c0001t0001g0311 |
2 | NA18940.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.782+5198_782+5213d others(18): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | |||||||
| chr10:103339810 | AACACACA others(11): Show |
A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0307 |
2 | NA18984.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.782+5196_782+5213d others(20): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339810 | |||||||
| chr10:103339811 | AC | A | 7 | a0001c0001t0001g0175 a0001c0001t0001g0179 a0001c0001t0001g0206 others(4): Show |
7 | HG00639.hp2 HG00735.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.782+5212delG | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | |||||||
| chr10:103339811 | ACAC | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0178 a0001c0001t0001g0187 others(6): Show |
9 | HG00642.hp2 HG02300.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.782+5210_782+5212d others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | |||||||
| chr10:103339811 | ACACAC | A | 5 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0218 others(2): Show |
5 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(2): Show |
intron_variant | MODIFIER | c.782+5208_782+5212d others(7): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | |||||||
| chr10:103339811 | ACACACAC others(2): Show |
A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0240 |
3 | HG02135.hp2 HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.782+5204_782+5212d others(11): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | |||||||
| chr10:103339811 | ACACACAC others(4): Show |
A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0333 |
2 | NA18953.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.782+5202_782+5212d others(13): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | |||||||
| chr10:103339811 | ACACACAC others(8): Show |
A | 4 | a0001c0001t0001g0185 a0001c0001t0001g0248 a0001c0001t0001g0314 others(1): Show |
4 | HG00558.hp2 HG02258.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.782+5198_782+5212d others(17): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | |||||||
| chr10:103339811 | ACACACAC others(10): Show |
A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0215 others(27): Show |
33 | HG00423.hp2 HG01257.hp2 HG01361.hp1 others(30): Show |
intron_variant | MODIFIER | c.782+5196_782+5212d others(19): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339811 | |||||||
| chr10:103339812 | C | A | 26 | a0001c0001t0001g0008 a0001c0001t0001g0176 a0001c0001t0001g0177 others(23): Show |
26 | HG00099.hp2 HG00621.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.782+5212G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339812 | |||||||
| chr10:103339814 | C | A | 30 | a0001c0001t0001g0179 a0001c0001t0001g0183 a0001c0001t0001g0184 others(27): Show |
30 | HG00323.hp1 HG00639.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.782+5210G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339814 | |||||||
| chr10:103339816 | C | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0178 a0001c0001t0001g0184 others(19): Show |
22 | HG00642.hp2 HG00735.hp1 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.782+5208G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339816 | |||||||
| chr10:103339818 | C | A | 21 | a0001c0001t0001g0211 a0001c0001t0001g0218 a0001c0001t0001g0224 others(18): Show |
21 | HG00438.hp2 HG00558.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.782+5206G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339818 | |||||||
| chr10:103339820 | C | A | 16 | a0001c0001t0001g0226 a0001c0001t0001g0312 a0001c0001t0001g0313 others(13): Show |
16 | HG00408.hp1 HG00438.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.782+5204G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339820 | |||||||
| chr10:103339822 | C | A | 12 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0060 others(9): Show |
12 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.782+5202G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339822 | |||||||
| chr10:103339824 | C | A | 14 | a0001c0001t0001g0244 a0001c0001t0001g0333 a0002c0002t0001g0058 others(11): Show |
14 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.782+5200G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339824 | |||||||
| chr10:103339826 | C | A | 11 | a0002c0002t0001g0058 a0002c0002t0001g0060 a0002c0002t0001g0061 others(8): Show |
11 | HG00735.hp1 HG01109.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.782+5198G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339826 | |||||||
| chr10:103339828 | C | A | 11 | a0001c0001t0001g0248 a0001c0001t0001g0311 a0001c0001t0001g0314 others(8): Show |
11 | HG00558.hp2 HG00735.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.782+5196G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339828 | |||||||
| chr10:103339830 | C | A | 30 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0215 others(27): Show |
33 | HG01257.hp2 HG01361.hp1 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.782+5194G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103339830 | |||||||
| chr10:103340007 | C | CA | 40 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(37): Show |
40 | HG00099.hp1 HG00408.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.782+5016dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340007 | |||||||
| chr10:103340007 | C | CAA | 108 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0006 others(105): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.782+5015_782+5016d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340007 | |||||||
| chr10:103340007 | C | CAAA | 17 | a0002c0002t0001g0022 a0002c0002t0001g0033 a0002c0002t0001g0038 others(14): Show |
17 | HG01192.hp1 HG01346.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.782+5014_782+5016d others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340007 | |||||||
| chr10:103340130 | T | C | 1 | a0001c0001t0001g0348 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.782+4894A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340130 | |||||||
| chr10:103340180 | GA | G | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0258 others(31): Show |
38 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.782+4843delT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340180 | |||||||
| chr10:103340180 | GAA | G | 10 | a0001c0001t0001g0177 a0001c0001t0001g0186 a0001c0001t0001g0273 others(7): Show |
10 | HG00733.hp2 HG01074.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.782+4842_782+4843d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340180 | |||||||
| chr10:103340180 | GAAA | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0239 others(43): Show |
51 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.782+4841_782+4843d others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340180 | |||||||
| chr10:103340180 | GAAAA | G | 58 | a0001c0001t0001g0252 a0002c0002t0001g0006 a0002c0002t0001g0045 others(55): Show |
59 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.782+4840_782+4843d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340180 | |||||||
| chr10:103340194 | A | ATATAT | 3 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0033 |
3 | HG02486.hp1 HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.782+4829_782+4830i others(7): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340194 | |||||||
| chr10:103340194 | A | T | 2 | a0002c0002t0001g0023 a0002c0002t0001g0075 |
2 | HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.782+4830T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340194 | |||||||
| chr10:103340196 | A | AAT | 6 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(3): Show |
7 | HG01884.hp2 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.782+4827_782+4828i others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340196 | |||||||
| chr10:103340196 | A | AT | 4 | a0001c0001t0003g0200 a0001c0001t0003g0203 a0001c0001t0003g0204 others(1): Show |
4 | HG01169.hp1 HG03516.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.782+4827_782+4828i others(3): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340196 | |||||||
| chr10:103340196 | A | T | 31 | a0001c0001t0003g0198 a0001c0001t0003g0202 a0002c0002t0001g0014 others(28): Show |
31 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.782+4828T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340196 | |||||||
| chr10:103340196 | AAAAT | A | 16 | a0002c0002t0001g0003 a0002c0002t0001g0073 a0002c0002t0001g0080 others(13): Show |
17 | HG00323.hp2 HG00733.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.782+4824_782+4827d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340196 | |||||||
| chr10:103340197 | AAAT | A | 18 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0276 others(15): Show |
18 | HG01884.hp1 HG01928.hp1 HG02135.hp2 others(15): Show |
intron_variant | MODIFIER | c.782+4824_782+4826d others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340197 | |||||||
| chr10:103340198 | A | ATATATAT others(10): Show |
1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.782+4825_782+4826i others(19): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340198 | |||||||
| chr10:103340198 | A | T | 83 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0179 others(80): Show |
86 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.782+4826T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340198 | |||||||
| chr10:103340198 | AAT | A | 28 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0187 others(25): Show |
28 | HG00438.hp2 HG00558.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.782+4824_782+4825d others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340198 | |||||||
| chr10:103340198 | AATAT | A | 10 | a0001c0001t0001g0285 a0001c0001t0001g0289 a0002c0002t0001g0058 others(7): Show |
10 | HG00323.hp1 HG00735.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.782+4822_782+4825d others(6): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340198 | |||||||
| chr10:103340199 | AT | A | 8 | a0001c0001t0001g0175 a0001c0001t0001g0178 a0001c0001t0001g0188 others(5): Show |
8 | HG00642.hp2 HG00735.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+4824delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340199 | |||||||
| chr10:103340199 | ATAT | A | 68 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0184 others(65): Show |
71 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.782+4822_782+4824d others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340199 | |||||||
| chr10:103340199 | ATATAT | A | 5 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0001g0065 others(2): Show |
5 | HG01109.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.782+4820_782+4824d others(7): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340199 | |||||||
| chr10:103340200 | T | A | 9 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0208 others(6): Show |
9 | HG00738.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.782+4824A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340200 | |||||||
| chr10:103340202 | T | A | 23 | a0001c0001t0001g0175 a0001c0001t0001g0182 a0001c0001t0001g0183 others(20): Show |
23 | HG00438.hp2 HG00558.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.782+4822A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340202 | |||||||
| chr10:103340204 | T | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0183 a0001c0001t0001g0188 others(52): Show |
57 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.782+4820A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340204 | |||||||
| chr10:103340206 | T | A | 10 | a0001c0001t0001g0345 a0002c0002t0001g0058 a0002c0002t0001g0059 others(7): Show |
10 | HG01099.hp1 HG01109.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.782+4818A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340206 | |||||||
| chr10:103340342 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.782+4682G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340342 | |||||||
| chr10:103340396 | G | C | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+4628C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340396 | |||||||
| chr10:103340600 | A | AT | 8 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(5): Show |
8 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.782+4423dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340600 | |||||||
| chr10:103340600 | AT | A | 15 | a0001c0001t0001g0236 a0001c0001t0001g0345 a0002c0002t0001g0058 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.782+4423delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340600 | |||||||
| chr10:103340700 | G | A | 1 | a0002c0002t0001g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.782+4324C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340700 | |||||||
| chr10:103340755 | G | T | 1 | a0002c0002t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.782+4269C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340755 | |||||||
| chr10:103340848 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.782+4176G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103340848 | |||||||
| chr10:103341210 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.782+3814G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341210 | |||||||
| chr10:103341278 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.782+3746G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341278 | |||||||
| chr10:103341609 | T | C | 1 | a0002c0002t0001g0144 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.782+3415A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341609 | |||||||
| chr10:103341688 | C | T | 2 | a0002c0002t0001g0095 a0002c0002t0001g0096 |
2 | NA18612.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.782+3336G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341688 | |||||||
| chr10:103341733 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.782+3291A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341733 | |||||||
| chr10:103341798 | C | T | 4 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG02258.hp1 HG02559.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+3226G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341798 | |||||||
| chr10:103341944 | C | T | 24 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(21): Show |
26 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.782+3080G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341944 | |||||||
| chr10:103341955 | C | G | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.782+3069G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103341955 | |||||||
| chr10:103342018 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0018 a0002c0002t0001g0019 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.782+3006C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342018 | |||||||
| chr10:103342202 | C | T | 1 | a0001c0001t0001g0333 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.782+2822G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342202 | |||||||
| chr10:103342223 | T | C | 2 | a0001c0001t0001g0291 a0001c0001t0001g0332 |
2 | HG03239.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.782+2801A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342223 | |||||||
| chr10:103342346 | G | A | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.782+2678C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342346 | |||||||
| chr10:103342543 | T | C | 2 | a0002c0002t0001g0062 a0002c0002t0001g0063 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.782+2481A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342543 | |||||||
| chr10:103342701 | T | C | 1 | a0002c0002t0001g0069 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.782+2323A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342701 | |||||||
| chr10:103342776 | T | C | 1 | a0002c0002t0001g0019 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.782+2248A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342776 | |||||||
| chr10:103342788 | T | C | 1 | a0002c0002t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.782+2236A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342788 | |||||||
| chr10:103342919 | A | ATG | 343 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(340): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.782+2104_782+2105i others(4): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342919 | |||||||
| chr10:103342964 | T | C | 11 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(8): Show |
11 | HG02258.hp1 HG02559.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.782+2060A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103342964 | |||||||
| chr10:103343007 | C | A | 1 | a0001c0001t0001g0345 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.782+2017G>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343007 | |||||||
| chr10:103343208 | G | A | 100 | a0001c0001t0001g0255 a0002c0002t0001g0003 a0002c0002t0001g0006 others(97): Show |
103 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.782+1816C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343208 | |||||||
| chr10:103343219 | C | T | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.782+1805G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343219 | |||||||
| chr10:103343257 | C | T | 1 | a0002c0002t0004g0020 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.782+1767G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343257 | |||||||
| chr10:103343533 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.782+1491C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343533 | |||||||
| chr10:103343797 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.782+1227G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343797 | |||||||
| chr10:103343811 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.782+1213G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343811 | |||||||
| chr10:103343832 | C | CAAAAAAA others(2): Show |
10 | a0001c0001t0001g0338 a0001c0001t0001g0341 a0001c0001t0001g0348 others(7): Show |
10 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.782+1183_782+1191d others(11): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | |||||||
| chr10:103343832 | C | CAAAAAAA others(3): Show |
175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(172): Show |
187 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.782+1182_782+1191d others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | |||||||
| chr10:103343832 | C | CAAAAAAA others(4): Show |
94 | a0001c0001t0001g0011 a0001c0001t0001g0176 a0001c0001t0001g0181 others(91): Show |
97 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.782+1181_782+1191d others(13): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | |||||||
| chr10:103343832 | C | CAAAAAAA others(5): Show |
40 | a0001c0001t0001g0005 a0001c0001t0001g0184 a0001c0001t0001g0191 others(37): Show |
42 | HG00621.hp2 HG00639.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.782+1180_782+1191d others(14): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | |||||||
| chr10:103343832 | C | CAAAAAAA others(6): Show |
16 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0248 others(13): Show |
16 | HG00558.hp2 HG00735.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.782+1179_782+1191d others(15): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | |||||||
| chr10:103343832 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0250 a0001c0001t0001g0333 a0001c0001t0001g0334 |
3 | HG02027.hp1 NA18940.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.782+1178_782+1191d others(16): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343832 | |||||||
| chr10:103343847 | A | AAAAAAAA others(3): Show |
1 | a0002c0002t0004g0016 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.782+1176_782+1177i others(12): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343847 | |||||||
| chr10:103343941 | C | G | 1 | a0002c0002t0001g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.782+1083G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343941 | |||||||
| chr10:103343970 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.782+1054A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103343970 | |||||||
| chr10:103344166 | G | A | 1 | a0002c0002t0001g0014 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.782+858C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344166 | |||||||
| chr10:103344273 | C | CT | 9 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0184 others(6): Show |
9 | HG00735.hp2 HG01192.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.782+750dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344273 | |||||||
| chr10:103344273 | CT | C | 19 | a0001c0001t0001g0238 a0001c0001t0001g0338 a0001c0001t0003g0009 others(16): Show |
21 | HG01074.hp1 HG01081.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.782+750delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344273 | |||||||
| chr10:103344326 | C | T | 169 | a0001c0001t0001g0255 a0001c0001t0003g0009 a0001c0001t0003g0010 others(166): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.782+698G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344326 | |||||||
| chr10:103344365 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.782+659C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344365 | |||||||
| chr10:103344668 | G | T | 182 | a0001c0001t0001g0255 a0001c0001t0003g0009 a0001c0001t0003g0010 others(179): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.782+356C>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344668 | |||||||
| chr10:103344758 | C | T | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 |
3 | HG02071.hp2 HG02155.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.782+266G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344758 | |||||||
| chr10:103344766 | C | T | 1 | a0002c0002t0001g0015 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.782+258G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 6/9 | chr10 | 103344766 | |||||||
| chr10:103345155 | T | C | 1 | a0002c0002t0001g0014 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.674-23A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345155 | |||||||
| chr10:103345273 | T | C | 2 | a0002c0002t0001g0161 a0002c0002t0001g0162 |
2 | NA18959.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.674-141A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345273 | |||||||
| chr10:103345496 | C | T | 1 | a0002c0002t0001g0014 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.674-364G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345496 | |||||||
| chr10:103345508 | CT | C | 166 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0192 others(163): Show |
173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.674-377delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345508 | |||||||
| chr10:103345547 | G | A | 12 | a0002c0002t0001g0058 a0002c0002t0001g0059 a0002c0002t0001g0060 others(9): Show |
12 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.674-415C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345547 | |||||||
| chr10:103345949 | T | C | 3 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0205 |
3 | HG01891.hp1 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.674-817A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103345949 | |||||||
| chr10:103346197 | A | T | 6 | a0002c0002t0001g0059 a0002c0002t0001g0062 a0002c0002t0001g0063 others(3): Show |
6 | HG00735.hp1 HG01099.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.673+1041T>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103346197 | |||||||
| chr10:103346222 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.673+1016A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103346222 | |||||||
| chr10:103346224 | G | A | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.673+1014C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103346224 | |||||||
| chr10:103346408 | G | A | 1 | a0002c0002t0002g0163 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.673+830C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103346408 | |||||||
| chr10:103347176 | A | C | 1 | a0001c0001t0001g0251 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.673+62T>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 5/9 | chr10 | 103347176 | |||||||
| chr10:103347636 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.558-186A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347636 | |||||||
| chr10:103347681 | T | C | 1 | a0001c0001t0001g0353 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.558-231A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347681 | |||||||
| chr10:103347707 | T | A | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.558-257A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347707 | |||||||
| chr10:103347713 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
150 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.558-263C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347713 | |||||||
| chr10:103347721 | T | A | 1 | a0002c0002t0001g0069 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.558-271A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347721 | |||||||
| chr10:103347819 | T | C | 1 | a0002c0002t0001g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.558-369A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347819 | |||||||
| chr10:103347836 | G | A | 1 | a0002c0002t0001g0056 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.558-386C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347836 | |||||||
| chr10:103347847 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.558-397G>A | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347847 | |||||||
| chr10:103347886 | G | A | 1 | a0001c0001t0001g0335 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.558-436C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347886 | |||||||
| chr10:103347999 | T | G | 1 | a0001c0001t0001g0336 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.558-549A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103347999 | |||||||
| chr10:103348005 | TC | T | 342 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(339): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.558-556delG | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348005 | |||||||
| chr10:103348333 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+383A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348333 | |||||||
| chr10:103348334 | T | A | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+382A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348334 | |||||||
| chr10:103348335 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+381A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348335 | |||||||
| chr10:103348336 | T | G | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+380A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348336 | |||||||
| chr10:103348337 | T | A | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+379A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348337 | |||||||
| chr10:103348338 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+378A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348338 | |||||||
| chr10:103348339 | T | A | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+377A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348339 | |||||||
| chr10:103348340 | G | C | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+376C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348340 | |||||||
| chr10:103348340 | GT | G | 160 | a0001c0001t0001g0345 a0002c0002t0001g0002 a0002c0002t0001g0003 others(157): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.557+375delA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348340 | |||||||
| chr10:103348341 | T | G | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+375A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348341 | |||||||
| chr10:103348342 | T | A | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+374A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348342 | |||||||
| chr10:103348343 | T | C | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+373A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348343 | |||||||
| chr10:103348344 | T | G | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+372A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348344 | |||||||
| chr10:103348345 | T | A | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+371A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348345 | |||||||
| chr10:103348347 | T | G | 1 | a0001c0001t0001g0337 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.557+369A>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348347 | |||||||
| chr10:103348687 | T | C | 1 | a0002c0002t0001g0070 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.557+29A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348687 | |||||||
| chr10:103348698 | T | C | 152 | a0002c0002t0001g0002 a0002c0002t0001g0003 a0002c0002t0001g0006 others(149): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.557+18A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 3/9 | chr10 | 103348698 | |||||||
| chr10:103348890 | G | A | 1 | a0002c0002t0001g0164 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.460+10C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 2/9 | chr10 | 103348890 | |||||||
| chr10:103349117 | G | C | 1 | a0002c0002t0001g0057 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.361-118C>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349117 | |||||||
| chr10:103349154 | T | C | 1 | a0001c0001t0001g0338 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.361-155A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349154 | |||||||
| chr10:103349404 | T | A | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.361-405A>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349404 | |||||||
| chr10:103349460 | T | C | 1 | a0002c0002t0001g0165 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.361-461A>G | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349460 | |||||||
| chr10:103349479 | G | GT | 250 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(247): Show |
264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.361-481dupA | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349479 | |||||||
| chr10:103349479 | G | GTT | 33 | a0001c0001t0001g0007 a0001c0001t0001g0183 a0001c0001t0001g0239 others(30): Show |
34 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.361-482_361-481dup others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349479 | |||||||
| chr10:103349479 | G | GTTT | 34 | a0002c0002t0001g0002 a0002c0002t0001g0014 a0002c0002t0001g0015 others(31): Show |
36 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(33): Show |
intron_variant | MODIFIER | c.361-483_361-481dup others(3): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349479 | |||||||
| chr10:103349512 | CCT | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.361-515_361-514del others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349512 | |||||||
| chr10:103349711 | G | A | 1 | a0002c0002t0001g0168 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.361-712C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103349711 | |||||||
| chr10:103350083 | A | AAAAAC | 11 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0175 others(8): Show |
13 | HG00639.hp2 HG00642.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.360+619_360+623dup others(5): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350083 | |||||||
| chr10:103350083 | A | AAAAACAA others(3): Show |
2 | a0002c0002t0001g0072 a0002c0002t0001g0073 |
2 | HG02083.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.360+614_360+623dup others(10): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350083 | |||||||
| chr10:103350176 | G | A | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.360+531C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350176 | |||||||
| chr10:103350267 | C | CA | 112 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0001c0001t0001g0342 others(109): Show |
115 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.360+439dupT | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350267 | |||||||
| chr10:103350267 | C | CAA | 6 | a0002c0002t0001g0169 a0002c0002t0001g0170 a0002c0002t0001g0171 others(3): Show |
6 | HG00280.hp1 HG01261.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.360+438_360+439dup others(2): Show |
PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350267 | |||||||
| chr10:103350624 | C | G | 1 | a0002c0004t0001g0013 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.360+83G>C | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350624 | |||||||
| chr10:103350684 | G | A | 1 | a0001c0001t0001g0354 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.360+23C>T | PCGF6 | ENSG00000156374.16 | transcript | ENST00000369847.4 | protein_coding | 1/9 | chr10 | 103350684 |