Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26024 |
| ensemblid | ENSG00000106246.18 |
| hgncid | 22198 |
| symbol | PTCD1 |
| name | pentatricopeptide repeat domain 1 |
| refseq_nuc | NM_015545.4 |
| refseq_prot | NP_056360.2 |
| ensembl_nuc | ENST00000292478.9 |
| ensembl_prot | ENSP00000292478.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 99416739 |
| end | 99438798 |
| strand | - |
| ver | v1.2 |
| region | chr7:99416739-99438798 |
| region5000 | chr7:99411739-99443798 |
| regionname0 | PTCD1_chr7_99416739_99438798 |
| regionname5000 | PTCD1_chr7_99411739_99443798 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 700 | 343 | 78 | 57 | 157 | 15 | 34 | 122 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0002 | 0/0 | 700 | 12 | 4 | 1 | 6 | 1 | 0 | 5 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0003 | 0/0 | 700 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0004 | 0/0 | 700 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0005 | 0/0 | 700 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0006 | 0/0 | 700 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0007 | 0/0 | 700 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0008 | 0/0 | 700 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0009 | 0/0 | 128 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(123): Show |
chr7 | 99411739 | 99443798 |
| a0010 | 0/0 | 700 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0011 | 0/0 | 700 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0012 | 0/0 | 700 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0013 | 0/0 | 700 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0014 | 0/0 | 700 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0015 | 0/0 | 700 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| a0016 | 0/0 | 700 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | MDFVR others(695): Show |
chr7 | 99411739 | 99443798 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2100 | 195 | 32 | 45 | 91 | 9 | 16 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0001c0002 | 0/0 | 2100 | 89 | 7 | 5 | 60 | 1 | 16 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0001c0003 | 0/0 | 2100 | 38 | 24 | 7 | 1 | 4 | 2 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0001c0005 | 0/0 | 2100 | 6 | 6 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0001c0008 | 0/0 | 2100 | 4 | 4 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0001c0009 | 0/0 | 2100 | 4 | 0 | 0 | 4 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0001c0012 | 0/0 | 2100 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0001c0014 | 0/0 | 2100 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0001c0017 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0001c0020 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0001c0021 | 0/0 | 2100 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0002c0004 | 0/0 | 2100 | 8 | 3 | 0 | 5 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0002c0010 | 0/0 | 2100 | 4 | 1 | 1 | 1 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0003c0006 | 0/0 | 2100 | 5 | 5 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0004c0007 | 0/0 | 2100 | 4 | 3 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0005c0011 | 0/0 | 2100 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0006c0013 | 0/0 | 2100 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0006c0016 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0007c0027 | 0/0 | 2100 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0008c0028 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0009c0015 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0010c0023 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0011c0018 | 0/0 | 2100 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0012c0025 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0013c0026 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0014c0024 | 0/0 | 2100 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0015c0019 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 | ||
| a0016c0022 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | ATGGA others(2095): Show |
chr7 | 99411739 | 99443798 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5464 | 146 | 4 | 38 | 79 | 8 | 15 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0002 | 0/0 | 5464 | 5 | 1 | 0 | 4 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0003 | 0/0 | 5464 | 5 | 5 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0004 | 0/0 | 5464 | 10 | 7 | 3 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0005 | 0/0 | 5464 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0006 | 0/0 | 5464 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0008 | 0/0 | 5464 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0010 | 0/0 | 5464 | 4 | 0 | 3 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0011 | 0/0 | 5464 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0012 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0013 | 0/0 | 5464 | 3 | 0 | 1 | 0 | 1 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0021 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0022 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0024 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0025 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0027 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0028 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0029 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0030 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0032 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0034 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0001t0039 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0002 | 0/0 | 5464 | 71 | 5 | 4 | 48 | 0 | 14 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0009 | 0/0 | 5463 | 5 | 0 | 0 | 5 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5458): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0014 | 0/0 | 5464 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0015 | 0/0 | 5464 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0017 | 0/0 | 5464 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0018 | 0/0 | 5463 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5458): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0020 | 0/0 | 5464 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0023 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0026 | 0/0 | 5463 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5458): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0031 | 0/0 | 5464 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0002t0037 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0003t0001 | 0/0 | 5464 | 7 | 1 | 5 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0003t0003 | 0/0 | 5464 | 21 | 16 | 1 | 0 | 2 | 2 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0003t0004 | 0/0 | 5464 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0003t0005 | 0/0 | 5464 | 5 | 5 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0003t0011 | 0/0 | 5464 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0003t0014 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0003t0015 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0003t0040 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0005t0006 | 0/0 | 5464 | 6 | 6 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0008t0007 | 0/0 | 5464 | 4 | 4 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0009t0001 | 0/0 | 5464 | 4 | 0 | 0 | 4 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0012t0007 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0012t0038 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0014t0016 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0014t0035 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0017t0016 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0020t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0001c0021t0001 | 0/0 | 5464 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0002c0004t0005 | 0/0 | 5464 | 7 | 2 | 0 | 5 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0002c0004t0007 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0002c0010t0005 | 0/0 | 5464 | 2 | 1 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0002c0010t0033 | 0/0 | 5464 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0002c0010t0041 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0003c0006t0004 | 0/0 | 5464 | 5 | 5 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0004c0007t0008 | 0/0 | 5464 | 3 | 2 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0004c0007t0036 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0005c0011t0012 | 0/0 | 5464 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0006c0013t0001 | 0/0 | 5464 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0006c0016t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0007c0027t0001 | 0/0 | 5464 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0008c0028t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0009c0015t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0010c0023t0019 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0011c0018t0001 | 0/0 | 5464 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0012c0025t0004 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0013c0026t0005 | 0/0 | 5464 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0014c0024t0001 | 0/0 | 5464 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0015c0019t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| a0016c0022t0001 | 0/0 | 5464 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | GGATT others(5459): Show |
chr7 | 99411739 | 99443798 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 35 | 0 | 9 | 17 | 1 | 7 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0074 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0004g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0008g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0010g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0010g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0011g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0012g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0013g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0013g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0013g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0021g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0022g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0024g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0025g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0027g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0028g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0029g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0030g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0032g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0034g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0001t0039g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0002 | 0/0 | 14 | 2 | 0 | 5 | 0 | 7 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0003 | 0/0 | 11 | 0 | 3 | 8 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0009g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0009g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0014g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0015g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0015g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0017g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0017g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0018g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0020g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0023g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0026g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0031g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0002t0037g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0001g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0001g0019 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0004g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0005g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0011g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0014g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0015g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0003t0040g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0005t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0005t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0005t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0005t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0005t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0008t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0008t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0008t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0008t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0009t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0009t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0009t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0009t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0012t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0012t0038g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0014t0016g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0014t0035g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0017t0016g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0020t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0001c0021t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0002c0004t0005g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0002c0004t0005g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0002c0004t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0002c0004t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0002c0004t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0002c0010t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0002c0010t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0002c0010t0033g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0002c0010t0041g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0003c0006t0004g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0003c0006t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0004c0007t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0004c0007t0008g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0004c0007t0008g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0004c0007t0036g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0005c0011t0012g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0006c0013t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0006c0013t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0006c0016t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0007c0027t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0008c0028t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0009c0015t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0010c0023t0019g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0011c0018t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0012c0025t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0013c0026t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0014c0024t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0015c0019t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| a0016c0022t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | GBR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00099 | hp2 | a0002 | c0010 | t0033 | g0060 | EUR | GBR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | GBR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00140 | hp2 | a0001 | c0021 | t0001 | g0096 | EUR | GBR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00280 | hp1 | a0001 | c0002 | t0031 | g0208 | EUR | FIN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | FIN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | FIN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0215 | EUR | FIN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0173 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00438 | hp2 | a0001 | c0009 | t0001 | g0117 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00558 | hp2 | a0001 | c0002 | t0023 | g0187 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00609 | hp1 | a0001 | c0001 | t0030 | g0098 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00621 | hp2 | a0001 | c0002 | t0026 | g0203 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0019 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0018 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0019 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01081 | hp2 | a0004 | c0007 | t0008 | g0239 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01106 | hp1 | a0001 | c0001 | t0013 | g0133 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0169 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01175 | hp2 | a0002 | c0010 | t0005 | g0057 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0182 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01243 | hp1 | a0001 | c0003 | t0004 | g0218 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01261 | hp2 | a0007 | c0027 | t0001 | g0147 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01346 | hp2 | a0001 | c0003 | t0003 | g0224 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01496 | hp1 | a0001 | c0002 | t0020 | g0191 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01516 | hp1 | a0001 | c0003 | t0003 | g0040 | EUR | IBS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01517 | hp1 | a0001 | c0003 | t0003 | g0040 | EUR | IBS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | IBS | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01884 | hp1 | a0001 | c0005 | t0006 | g0154 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01884 | hp2 | a0005 | c0011 | t0012 | g0012 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01891 | hp2 | a0004 | c0007 | t0008 | g0240 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01978 | hp2 | a0001 | c0001 | t0010 | g0045 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02055 | hp2 | a0001 | c0008 | t0007 | g0158 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02056 | hp1 | a0001 | c0002 | t0009 | g0200 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0193 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02083 | hp1 | a0001 | c0003 | t0015 | g0222 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02083 | hp2 | a0008 | c0028 | t0001 | g0148 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0019 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02165 | hp1 | a0009 | c0015 | t0001 | g0062 | EAS | CDX | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02165 | hp2 | a0001 | c0001 | t0021 | g0149 | EAS | CDX | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02257 | hp1 | a0010 | c0023 | t0019 | g0047 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02257 | hp2 | a0001 | c0003 | t0003 | g0008 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02258 | hp1 | a0001 | c0001 | t0034 | g0241 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0236 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02280 | hp2 | a0001 | c0001 | t0028 | g0106 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02293 | hp1 | a0001 | c0001 | t0010 | g0022 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02300 | hp1 | a0001 | c0001 | t0010 | g0022 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02451 | hp2 | a0001 | c0001 | t0039 | g0165 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02523 | hp2 | a0002 | c0010 | t0041 | g0248 | EAS | KHV | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02572 | hp1 | a0003 | c0006 | t0004 | g0010 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02602 | hp2 | a0001 | c0002 | t0015 | g0201 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02615 | hp2 | a0002 | c0004 | t0005 | g0024 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02630 | hp1 | a0001 | c0003 | t0014 | g0232 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02630 | hp2 | a0003 | c0006 | t0004 | g0010 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02647 | hp1 | a0002 | c0010 | t0005 | g0055 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02647 | hp2 | a0001 | c0014 | t0035 | g0245 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02717 | hp2 | a0001 | c0012 | t0007 | g0155 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02738 | hp2 | a0011 | c0018 | t0001 | g0135 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02809 | hp1 | a0001 | c0017 | t0016 | g0244 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02818 | hp2 | a0005 | c0011 | t0012 | g0012 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02886 | hp1 | a0003 | c0006 | t0004 | g0010 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02886 | hp2 | a0012 | c0025 | t0004 | g0167 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02895 | hp1 | a0001 | c0002 | t0014 | g0214 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02895 | hp2 | a0001 | c0003 | t0040 | g0233 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0041 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02896 | hp2 | a0001 | c0003 | t0005 | g0227 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0041 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02897 | hp2 | a0001 | c0002 | t0014 | g0213 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02922 | hp1 | a0001 | c0003 | t0003 | g0008 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02922 | hp2 | a0001 | c0005 | t0006 | g0033 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02965 | hp1 | a0001 | c0003 | t0005 | g0039 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02965 | hp2 | a0001 | c0003 | t0003 | g0231 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02970 | hp1 | a0001 | c0005 | t0006 | g0152 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0186 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03041 | hp2 | a0004 | c0007 | t0008 | g0238 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03098 | hp2 | a0003 | c0006 | t0004 | g0010 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03130 | hp1 | a0001 | c0014 | t0016 | g0246 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03130 | hp2 | a0001 | c0001 | t0022 | g0166 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0008 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03139 | hp2 | a0001 | c0003 | t0003 | g0228 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03195 | hp2 | a0003 | c0006 | t0004 | g0247 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0170 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03209 | hp2 | a0001 | c0003 | t0005 | g0219 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03225 | hp1 | a0002 | c0004 | t0005 | g0024 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03225 | hp2 | a0001 | c0003 | t0005 | g0039 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03239 | hp1 | a0001 | c0001 | t0013 | g0099 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03453 | hp1 | a0001 | c0005 | t0006 | g0153 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0164 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03486 | hp1 | a0001 | c0003 | t0005 | g0216 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03486 | hp2 | a0001 | c0008 | t0007 | g0053 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0209 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0021 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0179 | AFR | ESN | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03540 | hp1 | a0001 | c0012 | t0038 | g0156 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03540 | hp2 | a0001 | c0003 | t0003 | g0226 | AFR | GWD | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03579 | hp1 | a0013 | c0026 | t0005 | g0056 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03579 | hp2 | a0001 | c0005 | t0006 | g0151 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03654 | hp2 | a0001 | c0003 | t0003 | g0223 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03669 | hp1 | a0001 | c0003 | t0003 | g0221 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | STU | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03831 | hp1 | a0001 | c0002 | t0015 | g0175 | SAS | BEB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0035 | SAS | BEB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03927 | hp2 | a0014 | c0024 | t0001 | g0073 | SAS | BEB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0202 | SAS | STU | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0205 | SAS | BEB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | STU | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | STU | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18522 | hp1 | a0001 | c0003 | t0003 | g0008 | AFR | YRI | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18522 | hp2 | a0004 | c0007 | t0036 | g0210 | AFR | YRI | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | CHB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18906 | hp1 | a0001 | c0005 | t0006 | g0033 | AFR | YRI | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18906 | hp2 | a0002 | c0004 | t0007 | g0061 | AFR | YRI | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18939 | hp2 | a0002 | c0004 | t0005 | g0011 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18945 | hp1 | a0015 | c0019 | t0001 | g0131 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18948 | hp2 | a0001 | c0002 | t0009 | g0195 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18949 | hp1 | a0006 | c0013 | t0001 | g0139 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18950 | hp2 | a0001 | c0002 | t0009 | g0196 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18961 | hp1 | a0001 | c0002 | t0018 | g0044 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18963 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18965 | hp1 | a0016 | c0022 | t0001 | g0115 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18965 | hp2 | a0001 | c0002 | t0037 | g0178 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18971 | hp1 | a0002 | c0004 | t0005 | g0011 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18974 | hp1 | a0001 | c0001 | t0025 | g0134 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18975 | hp2 | a0001 | c0001 | t0010 | g0046 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18983 | hp1 | a0001 | c0001 | t0029 | g0108 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18989 | hp1 | a0002 | c0004 | t0005 | g0058 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18995 | hp1 | a0006 | c0016 | t0001 | g0190 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18995 | hp2 | a0006 | c0013 | t0001 | g0092 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18997 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18999 | hp2 | a0001 | c0002 | t0009 | g0038 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19002 | hp1 | a0002 | c0004 | t0005 | g0011 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19002 | hp2 | a0001 | c0001 | t0032 | g0105 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19004 | hp1 | a0001 | c0002 | t0017 | g0250 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19010 | hp1 | a0001 | c0009 | t0001 | g0116 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19010 | hp2 | a0001 | c0001 | t0027 | g0064 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19011 | hp1 | a0001 | c0001 | t0012 | g0113 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19012 | hp2 | a0001 | c0009 | t0001 | g0126 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19030 | hp2 | a0001 | c0003 | t0003 | g0217 | AFR | LWK | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | LWK | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | LWK | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19054 | hp1 | a0002 | c0004 | t0005 | g0059 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19056 | hp1 | a0001 | c0002 | t0017 | g0249 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19063 | hp1 | a0001 | c0009 | t0001 | g0078 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19078 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19086 | hp1 | a0001 | c0020 | t0001 | g0110 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19087 | hp1 | a0001 | c0002 | t0009 | g0038 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19087 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0020 | AFR | YRI | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA19240 | hp2 | a0001 | c0003 | t0003 | g0042 | AFR | YRI | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0008 | AFR | ASW | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ASW | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA20752 | hp1 | a0001 | c0003 | t0011 | g0225 | EUR | TSI | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA20805 | hp1 | a0001 | c0001 | t0013 | g0141 | EUR | TSI | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0002 | SAS | GIH | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG01123 | hp2 | a0001 | c0003 | t0001 | g0018 | AMR | CLM | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0181 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02486 | hp1 | a0001 | c0008 | t0007 | g0157 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0042 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG02559 | hp2 | a0005 | c0011 | t0012 | g0012 | AFR | ACB | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0243 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG03471 | hp2 | a0001 | c0008 | t0007 | g0159 | AFR | MSL | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG06807 | hp1 | a0001 | c0001 | t0024 | g0097 | AFR | USA | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0020 | AFR | USA | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | USA | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA20300 | hp2 | a0001 | c0003 | t0003 | g0220 | AFR | USA | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA21309 | hp1 | a0001 | c0003 | t0003 | g0229 | AFR | LWK | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| NA21309 | hp2 | a0001 | c0003 | t0003 | g0230 | AFR | LWK | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0074 | REF | REF | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | PTCD1_chr7_99411739_99443798 | PTCD1 | chr7 | 99411739 | 99443798 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99420037 | C | T | 1 | a0006 | 3 | NA18949.hp1 NA18995.hp1 NA18995.hp2 |
missense_variant | MODERATE | c.2033G>A | p.Arg678Gln | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2166/5464 | 2033/2103 | 678/700 | chr7 | 99420037 | |||
| chr7:99420071 | C | T | 1 | a0016 | 1 | NA18965.hp1 | missense_variant | MODERATE | c.1999G>A | p.Ala667Thr | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2132/5464 | 1999/2103 | 667/700 | chr7 | 99420071 | |||
| chr7:99423881 | T | C | 1 | a0010 | 1 | HG02257.hp1 | missense_variant | MODERATE | c.1814A>G | p.Tyr605Cys | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/8 | 1947/5464 | 1814/2103 | 605/700 | chr7 | 99423881 | |||
| chr7:99424966 | G | C | 1 | a0014 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.1566C>G | p.Phe522Leu | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/8 | 1699/5464 | 1566/2103 | 522/700 | chr7 | 99424966 | |||
| chr7:99425018 | G | A | 1 | a0005 | 3 | HG01884.hp2 HG02559.hp2 HG02818.hp2 |
missense_variant | MODERATE | c.1514C>T | p.Ser505Phe | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/8 | 1647/5464 | 1514/2103 | 505/700 | chr7 | 99425018 | |||
| chr7:99425112 | A | G | 1 | a0015 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.1420T>C | p.Phe474Leu | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/8 | 1553/5464 | 1420/2103 | 474/700 | chr7 | 99425112 | |||
| chr7:99425162 | G | A | 1 | a0004 | 4 | HG01081.hp2 HG01891.hp2 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.1370C>T | p.Thr457Met | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/8 | 1503/5464 | 1370/2103 | 457/700 | chr7 | 99425162 | |||
| chr7:99425190 | C | T | 1 | a0013 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.1342G>A | p.Val448Ile | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/8 | 1475/5464 | 1342/2103 | 448/700 | chr7 | 99425190 | |||
| chr7:99425250 | C | T | 1 | a0011 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1282G>A | p.Ala428Thr | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/8 | 1415/5464 | 1282/2103 | 428/700 | chr7 | 99425250 | |||
| chr7:99433303 | T | C | 1 | a0012 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.569A>G | p.Lys190Arg | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/8 | 702/5464 | 569/2103 | 190/700 | chr7 | 99433303 | |||
| chr7:99434856 | C | T | 1 | a0009 | 1 | HG02165.hp1 | stop_gained | HIGH | c.387G>A | p.Trp129* | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/8 | 520/5464 | 387/2103 | 129/700 | chr7 | 99434856 | |||
| chr7:99434894 | G | A | 2 | a0002 a0013 |
13 | HG00099.hp2 HG01175.hp2 HG02523.hp2 others(10): Show |
missense_variant | MODERATE | c.349C>T | p.Arg117Trp | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/8 | 482/5464 | 349/2103 | 117/700 | chr7 | 99434894 | |||
| chr7:99434936 | G | A | 1 | a0007 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.307C>T | p.Arg103Cys | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/8 | 440/5464 | 307/2103 | 103/700 | chr7 | 99434936 | |||
| chr7:99435112 | G | A | 1 | a0003 | 5 | HG02572.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
missense_variant | MODERATE | c.131C>T | p.Ala44Val | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/8 | 264/5464 | 131/2103 | 44/700 | chr7 | 99435112 | |||
| chr7:99435190 | A | G | 1 | a0004 | 4 | HG01081.hp2 HG01891.hp2 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.53T>C | p.Leu18Pro | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/8 | 186/5464 | 53/2103 | 18/700 | chr7 | 99435190 | |||
| chr7:99435197 | T | C | 1 | a0008 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.46A>G | p.Met16Val | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/8 | 179/5464 | 46/2103 | 16/700 | chr7 | 99435197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99419979 | A | G | 1 | a0001c0021 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.2091T>C | p.Leu697Leu | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2224/5464 | 2091/2103 | 697/700 | chr7 | 99419979 | |||
| chr7:99420057 | C | T | 1 | a0001c0020 | 1 | NA19086.hp1 | synonymous_variant | LOW | c.2013G>A | p.Pro671Pro | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2146/5464 | 2013/2103 | 671/700 | chr7 | 99420057 | |||
| chr7:99420114 | G | A | 3 | a0001c0009 a0002c0010 a0016c0022 |
9 | HG00099.hp2 HG00438.hp2 HG01175.hp2 others(6): Show |
synonymous_variant | LOW | c.1956C>T | p.Asp652Asp | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2089/5464 | 1956/2103 | 652/700 | chr7 | 99420114 | |||
| chr7:99423832 | G | A | 1 | a0014c0024 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.1863C>T | p.Asn621Asn | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/8 | 1996/5464 | 1863/2103 | 621/700 | chr7 | 99423832 | |||
| chr7:99424828 | C | T | 1 | a0001c0012 | 2 | HG02717.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.1704G>A | p.Pro568Pro | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/8 | 1837/5464 | 1704/2103 | 568/700 | chr7 | 99424828 | |||
| chr7:99425257 | G | T | 2 | a0001c0008 a0001c0012 |
6 | HG02055.hp2 HG02486.hp1 HG02717.hp2 others(3): Show |
synonymous_variant | LOW | c.1275C>A | p.Ala425Ala | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/8 | 1408/5464 | 1275/2103 | 425/700 | chr7 | 99425257 | |||
| chr7:99425368 | C | T | 2 | a0001c0014 a0001c0017 |
3 | HG02647.hp2 HG02809.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.1164G>A | p.Leu388Leu | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/8 | 1297/5464 | 1164/2103 | 388/700 | chr7 | 99425368 | |||
| chr7:99429106 | G | C | 1 | a0001c0014 | 2 | HG02647.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.912C>G | p.Leu304Leu | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/8 | 1045/5464 | 912/2103 | 304/700 | chr7 | 99429106 | |||
| chr7:99434835 | C | T | 2 | a0001c0002 a0006c0016 |
90 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
synonymous_variant | LOW | c.408G>A | p.Pro136Pro | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/8 | 541/5464 | 408/2103 | 136/700 | chr7 | 99434835 | |||
| chr7:99434970 | G | T | 1 | a0001c0003 | 38 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(35): Show |
synonymous_variant | LOW | c.273C>A | p.Thr91Thr | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/8 | 406/5464 | 273/2103 | 91/700 | chr7 | 99434970 | |||
| chr7:99435054 | C | G | 1 | a0003c0006 | 5 | HG02572.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
synonymous_variant | LOW | c.189G>C | p.Thr63Thr | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/8 | 322/5464 | 189/2103 | 63/700 | chr7 | 99435054 | |||
| chr7:99435054 | C | T | 1 | a0001c0005 | 6 | HG01884.hp1 HG02922.hp2 HG02970.hp1 others(3): Show |
synonymous_variant | LOW | c.189G>A | p.Thr63Thr | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/8 | 322/5464 | 189/2103 | 63/700 | chr7 | 99435054 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99416772 | G | A | 1 | a0001c0001t0029 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3195C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 3195 | chr7 | 99416772 | ||||||
| chr7:99417013 | CT | C | 3 | a0001c0002t0009 a0001c0002t0018 a0001c0002t0026 |
7 | HG00621.hp2 HG02056.hp1 NA18948.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2953delA | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2953 | chr7 | 99417013 | ||||||
| chr7:99417144 | C | A | 15 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(12): Show |
41 | HG01081.hp1 HG01081.hp2 HG01167.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2823G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2823 | chr7 | 99417144 | ||||||
| chr7:99417287 | A | G | 2 | a0001c0012t0038 a0004c0007t0036 |
2 | HG03540.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2680T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2680 | chr7 | 99417287 | ||||||
| chr7:99417304 | C | T | 3 | a0001c0014t0016 a0001c0014t0035 a0001c0017t0016 |
3 | HG02647.hp2 HG02809.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2663G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2663 | chr7 | 99417304 | ||||||
| chr7:99417361 | T | C | 34 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(31): Show |
99 | HG00099.hp2 HG01081.hp1 HG01081.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2606A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2606 | chr7 | 99417361 | ||||||
| chr7:99417442 | T | C | 1 | a0001c0001t0034 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2525A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2525 | chr7 | 99417442 | ||||||
| chr7:99417802 | A | G | 1 | a0001c0001t0028 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2165T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2165 | chr7 | 99417802 | ||||||
| chr7:99417828 | A | G | 1 | a0001c0014t0035 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2139T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2139 | chr7 | 99417828 | ||||||
| chr7:99417838 | T | C | 1 | a0001c0001t0030 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2129A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2129 | chr7 | 99417838 | ||||||
| chr7:99417947 | A | G | 1 | a0001c0001t0027 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2020T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 2020 | chr7 | 99417947 | ||||||
| chr7:99418070 | C | T | 3 | a0001c0014t0016 a0001c0014t0035 a0001c0017t0016 |
3 | HG02647.hp2 HG02809.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1897G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 1897 | chr7 | 99418070 | ||||||
| chr7:99418168 | T | C | 25 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(22): Show |
78 | HG01081.hp1 HG01081.hp2 HG01167.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1799A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 1799 | chr7 | 99418168 | ||||||
| chr7:99418213 | C | T | 11 | a0001c0001t0002 a0001c0001t0032 a0001c0002t0002 others(8): Show |
90 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1754G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 1754 | chr7 | 99418213 | ||||||
| chr7:99418220 | G | T | 1 | a0002c0010t0033 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1747C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 1747 | chr7 | 99418220 | ||||||
| chr7:99418259 | G | A | 15 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0032 others(12): Show |
97 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1708C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 1708 | chr7 | 99418259 | ||||||
| chr7:99418318 | A | G | 1 | a0001c0001t0032 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1649T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 1649 | chr7 | 99418318 | ||||||
| chr7:99418609 | G | A | 1 | a0001c0003t0040 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1358C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 1358 | chr7 | 99418609 | ||||||
| chr7:99418700 | G | T | 1 | a0001c0002t0031 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1267C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 1267 | chr7 | 99418700 | ||||||
| chr7:99418701 | A | G | 1 | a0001c0002t0031 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1266T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 1266 | chr7 | 99418701 | ||||||
| chr7:99418968 | T | G | 1 | a0001c0001t0022 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*999A>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 999 | chr7 | 99418968 | ||||||
| chr7:99419060 | G | C | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
196 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*907C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 907 | chr7 | 99419060 | ||||||
| chr7:99419064 | G | C | 1 | a0001c0001t0013 | 3 | HG01106.hp1 HG03239.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*903C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 903 | chr7 | 99419064 | ||||||
| chr7:99419083 | A | G | 1 | a0001c0002t0026 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*884T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 884 | chr7 | 99419083 | ||||||
| chr7:99419107 | A | G | 8 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0022 others(5): Show |
27 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*860T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 860 | chr7 | 99419107 | ||||||
| chr7:99419120 | G | A | 2 | a0001c0002t0014 a0001c0003t0014 |
3 | HG02630.hp1 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*847C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 847 | chr7 | 99419120 | ||||||
| chr7:99419242 | C | T | 1 | a0001c0001t0025 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*725G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 725 | chr7 | 99419242 | ||||||
| chr7:99419300 | C | T | 1 | a0001c0001t0024 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*667G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 667 | chr7 | 99419300 | ||||||
| chr7:99419327 | T | C | 1 | a0001c0002t0037 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*640A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 640 | chr7 | 99419327 | ||||||
| chr7:99419402 | C | T | 1 | a0001c0002t0023 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*565G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 565 | chr7 | 99419402 | ||||||
| chr7:99419448 | C | T | 7 | a0001c0001t0006 a0001c0001t0022 a0001c0001t0039 others(4): Show |
16 | HG01884.hp1 HG02055.hp2 HG02451.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*519G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 519 | chr7 | 99419448 | ||||||
| chr7:99419508 | G | A | 1 | a0001c0012t0038 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 459 | chr7 | 99419508 | ||||||
| chr7:99419520 | C | G | 1 | a0001c0001t0021 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*447G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 447 | chr7 | 99419520 | ||||||
| chr7:99419563 | G | C | 1 | a0001c0001t0039 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 404 | chr7 | 99419563 | ||||||
| chr7:99419658 | G | A | 5 | a0001c0001t0003 a0001c0002t0015 a0001c0003t0003 others(2): Show |
30 | HG01346.hp2 HG01516.hp1 HG01517.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*309C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 309 | chr7 | 99419658 | ||||||
| chr7:99419660 | C | T | 1 | a0001c0002t0020 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*307G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 307 | chr7 | 99419660 | ||||||
| chr7:99419734 | G | A | 2 | a0001c0002t0015 a0001c0003t0015 |
3 | HG02083.hp1 HG02602.hp2 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*233C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 8/8 | 233 | chr7 | 99419734 | ||||||
| chr7:99438721 | G | A | 1 | a0002c0010t0041 | 1 | HG02523.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/8 | chr7 | 99438721 | |||||||
| chr7:99438734 | C | G | 1 | a0010c0023t0019 | 1 | HG02257.hp1 | 5_prime_UTR_variant | MODIFIER | c.-69G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/8 | 3492 | chr7 | 99438734 | ||||||
| chr7:99438738 | C | T | 1 | a0001c0001t0010 | 4 | HG01978.hp2 HG02293.hp1 HG02300.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-73G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/8 | 3496 | chr7 | 99438738 | ||||||
| chr7:99438767 | T | A | 1 | a0001c0002t0017 | 2 | NA19004.hp1 NA19056.hp1 |
5_prime_UTR_variant | MODIFIER | c.-102A>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/8 | 3525 | chr7 | 99438767 | ||||||
| chr7:99438770 | C | T | 1 | a0001c0002t0018 | 1 | NA18961.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/8 | 3528 | chr7 | 99438770 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99420208 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1921-59A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420208 | |||||||
| chr7:99420209 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1921-60G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420209 | |||||||
| chr7:99420214 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1921-65C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420214 | |||||||
| chr7:99420217 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1921-68C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420217 | |||||||
| chr7:99420220 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1921-71A>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420220 | |||||||
| chr7:99420233 | A | C | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1921-84T>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420233 | |||||||
| chr7:99420240 | T | G | 1 | a0001c0001t0001g0104 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1921-91A>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420240 | |||||||
| chr7:99420345 | A | G | 1 | a0001c0003t0003g0226 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1921-196T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420345 | |||||||
| chr7:99420383 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1921-234A>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420383 | |||||||
| chr7:99420393 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1921-244A>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420393 | |||||||
| chr7:99420409 | C | G | 1 | a0002c0004t0005g0059 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1921-260G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420409 | |||||||
| chr7:99420679 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1921-530C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420679 | |||||||
| chr7:99420685 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1921-536C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420685 | |||||||
| chr7:99420695 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0095 |
2 | HG01070.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1921-546C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420695 | |||||||
| chr7:99420696 | T | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0095 |
2 | HG01070.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1921-547A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420696 | |||||||
| chr7:99420701 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0095 |
2 | HG01070.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1921-552T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420701 | |||||||
| chr7:99420744 | G | A | 2 | a0001c0002t0002g0037 a0001c0002t0002g0192 |
3 | NA19009.hp2 NA19087.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1921-595C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420744 | |||||||
| chr7:99420754 | C | T | 1 | a0001c0003t0003g0042 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1921-605G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420754 | |||||||
| chr7:99420755 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1921-606C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420755 | |||||||
| chr7:99420852 | C | A | 1 | a0001c0002t0002g0176 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1921-703G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420852 | |||||||
| chr7:99420925 | C | T | 1 | a0001c0002t0002g0184 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1921-776G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99420925 | |||||||
| chr7:99421268 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1921-1119A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421268 | |||||||
| chr7:99421429 | TA | T | 82 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0031 others(79): Show |
132 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.1921-1281delT | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421429 | |||||||
| chr7:99421429 | TAA | T | 8 | a0001c0002t0002g0186 a0001c0002t0002g0189 a0001c0002t0002g0197 others(5): Show |
8 | HG00280.hp1 HG02897.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.1921-1282_1921-128 others(6): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421429 | |||||||
| chr7:99421441 | A | G | 1 | a0002c0010t0005g0055 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1921-1292T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421441 | |||||||
| chr7:99421444 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02132.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1921-1295T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421444 | |||||||
| chr7:99421472 | T | A | 2 | a0002c0004t0005g0024 a0002c0004t0007g0061 |
3 | HG02615.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1921-1323A>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421472 | |||||||
| chr7:99421580 | T | TA | 70 | a0001c0001t0001g0068 a0001c0001t0001g0083 a0001c0001t0001g0094 others(67): Show |
87 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.1921-1432dupT | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421580 | |||||||
| chr7:99421580 | T | TAA | 7 | a0001c0001t0001g0121 a0001c0001t0003g0236 a0001c0001t0004g0034 others(4): Show |
8 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.1921-1433_1921-143 others(6): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421580 | |||||||
| chr7:99421688 | G | C | 18 | a0001c0001t0004g0016 a0001c0001t0004g0034 a0001c0001t0004g0160 others(15): Show |
23 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.1921-1539C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421688 | |||||||
| chr7:99421699 | G | A | 2 | a0001c0003t0003g0041 a0001c0003t0003g0228 |
3 | HG02896.hp1 HG02897.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1921-1550C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421699 | |||||||
| chr7:99421748 | C | A | 1 | a0001c0020t0001g0110 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1921-1599G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421748 | |||||||
| chr7:99421942 | G | A | 1 | a0001c0003t0001g0019 | 3 | HG00639.hp1 HG01074.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1921-1793C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421942 | |||||||
| chr7:99421958 | C | G | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | NA18946.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1921-1809G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99421958 | |||||||
| chr7:99422197 | A | G | 25 | a0001c0001t0004g0016 a0001c0001t0004g0034 a0001c0001t0004g0160 others(22): Show |
30 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.1920+1578T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422197 | |||||||
| chr7:99422218 | C | T | 2 | a0001c0001t0006g0052 a0001c0001t0022g0166 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1920+1557G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422218 | |||||||
| chr7:99422261 | C | A | 1 | a0010c0023t0019g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1920+1514G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422261 | |||||||
| chr7:99422282 | G | A | 1 | a0004c0007t0008g0240 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1920+1493C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422282 | |||||||
| chr7:99422332 | C | T | 1 | a0013c0026t0005g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1920+1443G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422332 | |||||||
| chr7:99422422 | G | A | 1 | a0001c0008t0007g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1920+1353C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422422 | |||||||
| chr7:99422426 | C | T | 1 | a0001c0001t0010g0045 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1920+1349G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422426 | |||||||
| chr7:99422535 | T | C | 3 | a0001c0001t0002g0015 a0001c0001t0002g0084 a0001c0001t0032g0105 |
5 | HG02080.hp1 NA18946.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1920+1240A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422535 | |||||||
| chr7:99422548 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0212 |
2 | NA18941.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1920+1227T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422548 | |||||||
| chr7:99422550 | A | G | 2 | a0003c0006t0004g0010 a0003c0006t0004g0247 |
5 | HG02572.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1920+1225T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422550 | |||||||
| chr7:99422681 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0069 others(5): Show |
10 | HG00323.hp1 NA18941.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.1920+1094G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422681 | |||||||
| chr7:99422700 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1920+1075C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422700 | |||||||
| chr7:99422886 | G | A | 1 | a0001c0001t0028g0106 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1920+889C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422886 | |||||||
| chr7:99422908 | C | T | 1 | a0001c0003t0003g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1920+867G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99422908 | |||||||
| chr7:99423006 | T | G | 7 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0034g0241 others(4): Show |
7 | HG01081.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1920+769A>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423006 | |||||||
| chr7:99423031 | C | T | 1 | a0005c0011t0012g0012 | 3 | HG01884.hp2 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1920+744G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423031 | |||||||
| chr7:99423051 | G | T | 1 | a0001c0001t0005g0243 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1920+724C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423051 | |||||||
| chr7:99423074 | CCT | C | 2 | a0003c0006t0004g0010 a0003c0006t0004g0247 |
5 | HG02572.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1920+699_1920+700d others(4): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423074 | |||||||
| chr7:99423183 | A | G | 134 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(131): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1920+592T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423183 | |||||||
| chr7:99423244 | G | A | 1 | a0001c0001t0008g0021 | 3 | HG02451.hp1 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1920+531C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423244 | |||||||
| chr7:99423356 | G | A | 24 | a0001c0001t0004g0016 a0001c0001t0004g0034 a0001c0001t0004g0160 others(21): Show |
30 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.1920+419C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423356 | |||||||
| chr7:99423380 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1920+395C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423380 | |||||||
| chr7:99423380 | G | C | 16 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0017 others(13): Show |
33 | HG00597.hp2 HG01099.hp1 HG01192.hp1 others(30): Show |
intron_variant | MODIFIER | c.1920+395C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423380 | |||||||
| chr7:99423529 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1920+246G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423529 | |||||||
| chr7:99423722 | A | AG | 17 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0051 others(14): Show |
20 | HG00621.hp1 HG00621.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1920+52dupC | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 7/7 | chr7 | 99423722 | |||||||
| chr7:99423975 | C | T | 2 | a0001c0002t0017g0249 a0001c0002t0017g0250 |
2 | NA19004.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1738-18G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99423975 | |||||||
| chr7:99424000 | T | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG00738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1738-43A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99424000 | |||||||
| chr7:99424071 | C | G | 2 | a0003c0006t0004g0010 a0003c0006t0004g0247 |
5 | HG02572.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-114G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99424071 | |||||||
| chr7:99424139 | C | T | 2 | a0001c0002t0014g0213 a0001c0002t0014g0214 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1738-182G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99424139 | |||||||
| chr7:99424252 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1738-295A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99424252 | |||||||
| chr7:99424323 | T | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0211 |
3 | HG01258.hp1 HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1738-366A>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99424323 | |||||||
| chr7:99424359 | C | T | 3 | a0001c0014t0016g0246 a0001c0014t0035g0245 a0001c0017t0016g0244 |
3 | HG02647.hp2 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1738-402G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99424359 | |||||||
| chr7:99424376 | G | A | 1 | a0010c0023t0019g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1737+419C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99424376 | |||||||
| chr7:99424592 | C | T | 1 | a0001c0002t0002g0180 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1737+203G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99424592 | |||||||
| chr7:99424626 | C | A | 1 | a0001c0003t0011g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1737+169G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99424626 | |||||||
| chr7:99424705 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1737+90C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 6/7 | chr7 | 99424705 | |||||||
| chr7:99425623 | C | G | 134 | a0001c0001t0001g0090 a0001c0001t0002g0234 a0001c0001t0003g0043 others(131): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
splice_region_variant&intron_variant | LOW | c.916-7G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99425623 | |||||||
| chr7:99425731 | C | A | 1 | a0001c0012t0038g0156 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.916-115G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99425731 | |||||||
| chr7:99425795 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0031 others(28): Show |
46 | HG00099.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.916-179C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99425795 | |||||||
| chr7:99425806 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.916-190G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99425806 | |||||||
| chr7:99425838 | A | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0065 others(143): Show |
215 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.916-222T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99425838 | |||||||
| chr7:99425998 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.916-382C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99425998 | |||||||
| chr7:99426140 | GTCTCCC | G | 3 | a0001c0003t0003g0220 a0001c0003t0003g0226 a0001c0003t0003g0230 |
3 | HG03540.hp2 NA20300.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.916-530_916-525del others(6): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426140 | |||||||
| chr7:99426152 | CTCTCCCT others(16): Show |
C | 1 | a0001c0001t0001g0111 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.916-559_916-537del others(23): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426152 | |||||||
| chr7:99426173 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG01258.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.916-557G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426173 | |||||||
| chr7:99426188 | TCTCCCCA others(14): Show |
T | 55 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(52): Show |
72 | HG00323.hp2 HG00544.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.916-593_916-573del others(21): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426188 | |||||||
| chr7:99426209 | C | CCT | 90 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0065 others(87): Show |
142 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.916-595_916-594dup others(2): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426209 | |||||||
| chr7:99426216 | C | T | 1 | a0002c0004t0005g0058 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.916-600G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426216 | |||||||
| chr7:99426220 | A | G | 1 | a0001c0001t0002g0234 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.916-604T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426220 | |||||||
| chr7:99426270 | G | A | 2 | a0001c0001t0001g0112 a0001c0003t0003g0224 |
2 | HG00642.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.916-654C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426270 | |||||||
| chr7:99426279 | C | T | 2 | a0001c0002t0014g0213 a0001c0002t0014g0214 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.916-663G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426279 | |||||||
| chr7:99426306 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0065 others(16): Show |
25 | HG00099.hp2 HG00738.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.916-690G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426306 | |||||||
| chr7:99426424 | G | T | 2 | a0001c0001t0005g0243 a0001c0001t0011g0020 |
4 | HG02970.hp2 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.916-808C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426424 | |||||||
| chr7:99426439 | A | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0065 others(143): Show |
215 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.916-823T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426439 | |||||||
| chr7:99426460 | G | A | 1 | a0001c0001t0008g0021 | 3 | HG02451.hp1 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.916-844C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426460 | |||||||
| chr7:99426596 | A | AC | 30 | a0001c0001t0001g0013 a0001c0001t0001g0070 a0001c0001t0001g0080 others(27): Show |
32 | HG00597.hp1 HG00621.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.916-981dupG | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426596 | |||||||
| chr7:99426598 | C | T | 1 | a0001c0005t0006g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.916-982G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426598 | |||||||
| chr7:99426640 | G | T | 1 | a0002c0010t0005g0055 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.916-1024C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426640 | |||||||
| chr7:99426721 | A | G | 1 | a0001c0002t0002g0035 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.916-1105T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426721 | |||||||
| chr7:99426745 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.916-1129C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426745 | |||||||
| chr7:99426814 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.916-1198C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426814 | |||||||
| chr7:99426833 | G | A | 7 | a0001c0001t0001g0114 a0001c0001t0012g0113 a0001c0009t0001g0078 others(4): Show |
7 | HG00438.hp2 NA18965.hp1 NA19010.hp1 others(4): Show |
intron_variant | MODIFIER | c.916-1217C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426833 | |||||||
| chr7:99426867 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.916-1251C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426867 | |||||||
| chr7:99426905 | G | A | 1 | a0001c0003t0003g0229 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.916-1289C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426905 | |||||||
| chr7:99426977 | T | C | 144 | a0001c0001t0001g0006 a0001c0001t0001g0063 a0001c0001t0001g0065 others(141): Show |
213 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.916-1361A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426977 | |||||||
| chr7:99426989 | C | G | 2 | a0003c0006t0004g0010 a0003c0006t0004g0247 |
5 | HG02572.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.916-1373G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99426989 | |||||||
| chr7:99427012 | C | G | 1 | a0001c0008t0007g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.916-1396G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427012 | |||||||
| chr7:99427013 | C | T | 26 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0215 others(23): Show |
38 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.916-1397G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427013 | |||||||
| chr7:99427058 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.916-1442C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427058 | |||||||
| chr7:99427074 | G | A | 1 | a0004c0007t0036g0210 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.916-1458C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427074 | |||||||
| chr7:99427118 | C | T | 114 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(111): Show |
171 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.916-1502G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427118 | |||||||
| chr7:99427119 | C | T | 2 | a0001c0012t0007g0155 a0001c0012t0038g0156 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.916-1503G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427119 | |||||||
| chr7:99427143 | C | T | 114 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(111): Show |
171 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.916-1527G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427143 | |||||||
| chr7:99427179 | G | T | 1 | a0001c0001t0001g0028 | 2 | HG00642.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.916-1563C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427179 | |||||||
| chr7:99427208 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0138 a0001c0001t0001g0146 others(1): Show |
8 | HG00673.hp1 HG02083.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-1592C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427208 | |||||||
| chr7:99427242 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.916-1626C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427242 | |||||||
| chr7:99427277 | C | T | 114 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(111): Show |
171 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.916-1661G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427277 | |||||||
| chr7:99427321 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.916-1705G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427321 | |||||||
| chr7:99427326 | G | A | 3 | a0001c0002t0002g0017 a0001c0002t0002g0177 a0001c0002t0037g0178 |
5 | NA18944.hp1 NA18954.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.916-1710C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427326 | |||||||
| chr7:99427333 | C | T | 1 | a0001c0003t0003g0042 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.916-1717G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427333 | |||||||
| chr7:99427379 | G | A | 1 | a0013c0026t0005g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.915+1724C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427379 | |||||||
| chr7:99427405 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.915+1698C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427405 | |||||||
| chr7:99427452 | G | GGCCAGCC others(43): Show |
3 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0211 |
3 | HG01258.hp1 HG01496.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.915+1601_915+1650d others(52): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427452 | |||||||
| chr7:99427580 | G | A | 1 | a0001c0009t0001g0126 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.915+1523C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427580 | |||||||
| chr7:99427611 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.915+1492G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427611 | |||||||
| chr7:99427625 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.915+1478G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427625 | |||||||
| chr7:99427626 | G | A | 4 | a0001c0001t0010g0046 a0001c0014t0016g0246 a0001c0014t0035g0245 others(1): Show |
4 | HG02647.hp2 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.915+1477C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427626 | |||||||
| chr7:99427705 | C | T | 4 | a0001c0003t0001g0018 a0001c0003t0001g0019 a0001c0003t0001g0215 others(1): Show |
8 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+1398G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427705 | |||||||
| chr7:99427731 | T | G | 1 | a0001c0002t0002g0199 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.915+1372A>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427731 | |||||||
| chr7:99427814 | T | C | 1 | a0001c0001t0034g0241 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.915+1289A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427814 | |||||||
| chr7:99427866 | T | C | 8 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0011g0020 others(5): Show |
10 | HG01081.hp2 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.915+1237A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427866 | |||||||
| chr7:99427867 | G | C | 114 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(111): Show |
171 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.915+1236C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427867 | |||||||
| chr7:99427887 | A | T | 56 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(53): Show |
75 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.915+1216T>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427887 | |||||||
| chr7:99427968 | A | G | 134 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(131): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.915+1135T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427968 | |||||||
| chr7:99427984 | G | C | 134 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(131): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.915+1119C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99427984 | |||||||
| chr7:99428009 | T | C | 55 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(52): Show |
72 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(69): Show |
intron_variant | MODIFIER | c.915+1094A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428009 | |||||||
| chr7:99428271 | T | C | 20 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0011g0020 others(17): Show |
28 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.915+832A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428271 | |||||||
| chr7:99428402 | C | CA | 6 | a0001c0002t0002g0206 a0001c0002t0009g0200 a0001c0008t0007g0158 others(3): Show |
9 | HG02055.hp2 HG02056.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.915+700dupT | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428402 | |||||||
| chr7:99428402 | CA | C | 14 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0079 others(11): Show |
16 | HG00323.hp1 HG01081.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.915+700delT | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428402 | |||||||
| chr7:99428610 | G | A | 11 | a0001c0002t0002g0009 a0001c0002t0002g0194 a0001c0002t0002g0197 others(8): Show |
15 | HG00621.hp2 HG02056.hp1 NA18948.hp2 others(12): Show |
intron_variant | MODIFIER | c.915+493C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428610 | |||||||
| chr7:99428658 | G | A | 2 | a0002c0004t0005g0024 a0002c0004t0007g0061 |
3 | HG02615.hp2 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.915+445C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428658 | |||||||
| chr7:99428695 | C | T | 1 | a0001c0009t0001g0078 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.915+408G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428695 | |||||||
| chr7:99428722 | G | A | 1 | a0004c0007t0008g0239 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.915+381C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428722 | |||||||
| chr7:99428783 | G | T | 4 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0011g0020 others(1): Show |
6 | HG02258.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+320C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428783 | |||||||
| chr7:99428870 | A | G | 134 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(131): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.915+233T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428870 | |||||||
| chr7:99428952 | A | G | 1 | a0001c0002t0002g0179 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.915+151T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 5/7 | chr7 | 99428952 | |||||||
| chr7:99429214 | G | A | 55 | a0001c0002t0001g0188 a0001c0002t0002g0002 a0001c0002t0002g0003 others(52): Show |
93 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.814-10C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 4/7 | chr7 | 99429214 | |||||||
| chr7:99429285 | T | C | 1 | a0001c0002t0017g0250 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.814-81A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 4/7 | chr7 | 99429285 | |||||||
| chr7:99429380 | G | A | 3 | a0001c0002t0002g0202 a0001c0002t0015g0175 a0001c0002t0015g0201 |
3 | HG02602.hp2 HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.814-176C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 4/7 | chr7 | 99429380 | |||||||
| chr7:99429421 | T | C | 134 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(131): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.813+167A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 4/7 | chr7 | 99429421 | |||||||
| chr7:99429945 | C | T | 5 | a0001c0002t0002g0007 a0001c0002t0002g0017 a0001c0002t0002g0176 others(2): Show |
11 | NA18944.hp1 NA18945.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.595-139G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99429945 | |||||||
| chr7:99430025 | C | A | 1 | a0001c0003t0003g0230 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.595-219G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430025 | |||||||
| chr7:99430030 | G | A | 1 | a0001c0001t0003g0237 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.595-224C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430030 | |||||||
| chr7:99430193 | G | A | 1 | a0010c0023t0019g0047 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.595-387C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430193 | |||||||
| chr7:99430223 | T | C | 2 | a0001c0002t0017g0249 a0001c0002t0017g0250 |
2 | NA19004.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.595-417A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430223 | |||||||
| chr7:99430366 | G | A | 2 | a0001c0001t0005g0243 a0001c0001t0011g0020 |
4 | HG02970.hp2 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-560C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430366 | |||||||
| chr7:99430405 | A | G | 1 | a0001c0001t0013g0133 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.595-599T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430405 | |||||||
| chr7:99430454 | G | C | 2 | a0001c0001t0005g0242 a0001c0001t0034g0241 |
2 | HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.595-648C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430454 | |||||||
| chr7:99430523 | C | T | 1 | a0001c0003t0003g0041 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.595-717G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430523 | |||||||
| chr7:99430551 | C | G | 1 | a0001c0003t0003g0042 | 2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.595-745G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430551 | |||||||
| chr7:99430565 | T | G | 1 | a0001c0001t0005g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.595-759A>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430565 | |||||||
| chr7:99430627 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0128 |
3 | HG01074.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.595-821C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430627 | |||||||
| chr7:99430713 | G | A | 1 | a0001c0001t0005g0242 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.595-907C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99430713 | |||||||
| chr7:99431088 | T | C | 1 | a0001c0002t0026g0203 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.595-1282A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431088 | |||||||
| chr7:99431120 | A | T | 1 | a0001c0001t0001g0050 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.595-1314T>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431120 | |||||||
| chr7:99431166 | G | A | 2 | a0001c0008t0007g0159 a0005c0011t0012g0012 |
4 | HG01884.hp2 HG02559.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-1360C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431166 | |||||||
| chr7:99431184 | G | A | 1 | a0005c0011t0012g0012 | 3 | HG01884.hp2 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.595-1378C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431184 | |||||||
| chr7:99431201 | C | T | 1 | a0001c0001t0001g0027 | 2 | NA18951.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.595-1395G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431201 | |||||||
| chr7:99431456 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.595-1650T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431456 | |||||||
| chr7:99431634 | G | A | 1 | a0001c0001t0008g0021 | 3 | HG02451.hp1 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.594+1644C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431634 | |||||||
| chr7:99431654 | C | T | 136 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0002g0234 others(133): Show |
201 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.594+1624G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431654 | |||||||
| chr7:99431719 | C | T | 1 | a0001c0002t0015g0175 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.594+1559G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431719 | |||||||
| chr7:99431761 | A | G | 134 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(131): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.594+1517T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431761 | |||||||
| chr7:99431770 | G | A | 1 | a0001c0002t0002g0174 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.594+1508C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431770 | |||||||
| chr7:99431785 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0145 |
2 | NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.594+1493A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431785 | |||||||
| chr7:99431800 | G | C | 1 | a0001c0002t0002g0204 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.594+1478C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431800 | |||||||
| chr7:99431814 | C | G | 1 | a0005c0011t0012g0012 | 3 | HG01884.hp2 HG02559.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.594+1464G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431814 | |||||||
| chr7:99431948 | T | A | 5 | a0001c0003t0003g0008 a0001c0003t0003g0042 a0001c0003t0003g0231 others(2): Show |
10 | HG02257.hp2 HG02486.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.594+1330A>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99431948 | |||||||
| chr7:99432007 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.594+1271G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432007 | |||||||
| chr7:99432008 | G | A | 1 | a0001c0001t0010g0046 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.594+1270C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432008 | |||||||
| chr7:99432269 | CGTCCCTG others(1): Show |
C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0130 a0001c0001t0001g0132 others(1): Show |
4 | HG02004.hp1 NA18945.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+1001_594+1008d others(10): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432269 | |||||||
| chr7:99432288 | T | C | 1 | a0001c0001t0013g0133 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.594+990A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432288 | |||||||
| chr7:99432393 | C | A | 1 | a0001c0001t0005g0243 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.594+885G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432393 | |||||||
| chr7:99432393 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.594+885G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432393 | |||||||
| chr7:99432459 | C | A | 1 | a0004c0007t0008g0240 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.594+819G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432459 | |||||||
| chr7:99432464 | G | C | 2 | a0001c0001t0006g0052 a0001c0001t0022g0166 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.594+814C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432464 | |||||||
| chr7:99432485 | C | T | 19 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0011g0020 others(16): Show |
24 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.594+793G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432485 | |||||||
| chr7:99432537 | G | A | 1 | a0001c0001t0025g0134 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.594+741C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432537 | |||||||
| chr7:99432585 | C | T | 4 | a0004c0007t0008g0238 a0004c0007t0008g0239 a0004c0007t0008g0240 others(1): Show |
4 | HG01081.hp2 HG01891.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+693G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432585 | |||||||
| chr7:99432588 | AGCGCAGG others(10): Show |
A | 4 | a0001c0001t0006g0052 a0001c0001t0006g0164 a0001c0001t0022g0166 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+673_594+689del others(17): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432588 | |||||||
| chr7:99432605 | T | C | 106 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(103): Show |
163 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.594+673A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432605 | |||||||
| chr7:99432622 | T | C | 4 | a0001c0001t0006g0052 a0001c0001t0006g0164 a0001c0001t0022g0166 others(1): Show |
4 | HG02451.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+656A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432622 | |||||||
| chr7:99432624 | C | T | 5 | a0001c0003t0003g0040 a0001c0003t0003g0221 a0001c0003t0003g0223 others(2): Show |
6 | HG01346.hp2 HG01516.hp1 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+654G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432624 | |||||||
| chr7:99432718 | C | G | 1 | a0001c0002t0002g0207 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.594+560G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432718 | |||||||
| chr7:99432763 | C | T | 4 | a0004c0007t0008g0238 a0004c0007t0008g0239 a0004c0007t0008g0240 others(1): Show |
4 | HG01081.hp2 HG01891.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+515G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432763 | |||||||
| chr7:99432975 | G | T | 1 | a0001c0017t0016g0244 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.594+303C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99432975 | |||||||
| chr7:99433077 | C | T | 1 | a0001c0003t0003g0220 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.594+201G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99433077 | |||||||
| chr7:99433141 | C | G | 6 | a0001c0008t0007g0053 a0001c0008t0007g0157 a0001c0008t0007g0158 others(3): Show |
6 | HG02055.hp2 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.594+137G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99433141 | |||||||
| chr7:99433159 | A | T | 31 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(28): Show |
44 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.594+119T>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99433159 | |||||||
| chr7:99433185 | C | G | 1 | a0014c0024t0001g0073 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.594+93G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99433185 | |||||||
| chr7:99433255 | G | A | 1 | a0001c0003t0003g0217 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.594+23C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99433255 | |||||||
| chr7:99433266 | G | A | 1 | a0001c0017t0016g0244 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.594+12C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 3/7 | chr7 | 99433266 | |||||||
| chr7:99433523 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18960.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.454-105C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99433523 | |||||||
| chr7:99433599 | G | A | 1 | a0011c0018t0001g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.454-181C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99433599 | |||||||
| chr7:99433665 | T | C | 2 | a0001c0014t0016g0246 a0001c0014t0035g0245 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.454-247A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99433665 | |||||||
| chr7:99433868 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.454-450T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99433868 | |||||||
| chr7:99434009 | A | G | 6 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0069 others(3): Show |
8 | HG00323.hp1 NA18941.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.454-591T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434009 | |||||||
| chr7:99434021 | CAGCCTGG others(50): Show |
C | 52 | a0001c0002t0001g0188 a0001c0002t0002g0002 a0001c0002t0002g0003 others(49): Show |
88 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.454-660_454-604del others(57): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434021 | |||||||
| chr7:99434051 | C | CA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0076 a0001c0001t0001g0129 others(6): Show |
9 | HG02055.hp1 HG02897.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.454-634dupT | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434051 | |||||||
| chr7:99434060 | A | C | 2 | a0001c0001t0005g0243 a0001c0001t0011g0020 |
4 | HG02970.hp2 HG03471.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.454-642T>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434060 | |||||||
| chr7:99434150 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0138 a0001c0001t0001g0146 others(1): Show |
8 | HG00673.hp1 HG02083.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.453+640T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434150 | |||||||
| chr7:99434221 | G | A | 2 | a0001c0002t0002g0173 a0001c0002t0002g0174 |
2 | HG00438.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.453+569C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434221 | |||||||
| chr7:99434294 | A | G | 1 | a0002c0010t0005g0055 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.453+496T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434294 | |||||||
| chr7:99434351 | T | C | 3 | a0001c0014t0016g0246 a0001c0014t0035g0245 a0001c0017t0016g0244 |
3 | HG02647.hp2 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.453+439A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434351 | |||||||
| chr7:99434548 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.453+242C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434548 | |||||||
| chr7:99434573 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.453+217A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434573 | |||||||
| chr7:99434594 | C | CA | 11 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0142 others(8): Show |
13 | HG00738.hp1 HG00738.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.453+195dupT | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434594 | |||||||
| chr7:99434608 | T | A | 1 | a0001c0001t0001g0146 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.453+182A>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434608 | |||||||
| chr7:99434644 | G | T | 6 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG02056.hp2 NA18955.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.453+146C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434644 | |||||||
| chr7:99434776 | A | G | 54 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(51): Show |
71 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(68): Show |
intron_variant | MODIFIER | c.453+14T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 2/7 | chr7 | 99434776 | |||||||
| chr7:99435344 | A | G | 5 | a0001c0002t0002g0171 a0001c0002t0002g0172 a0001c0002t0002g0173 others(2): Show |
5 | HG00438.hp1 NA19067.hp2 NA19077.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26-76T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435344 | |||||||
| chr7:99435405 | G | C | 1 | a0001c0002t0002g0206 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-26-137C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435405 | |||||||
| chr7:99435502 | G | C | 2 | a0001c0001t0004g0034 a0001c0001t0004g0169 |
3 | HG01081.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-26-234C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435502 | |||||||
| chr7:99435677 | C | A | 1 | a0001c0002t0002g0207 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-26-409G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435677 | |||||||
| chr7:99435722 | G | C | 5 | a0001c0001t0001g0150 a0001c0001t0010g0022 a0001c0001t0010g0045 others(2): Show |
6 | HG01978.hp2 HG02165.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.-26-454C>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435722 | |||||||
| chr7:99435814 | A | G | 1 | a0001c0002t0002g0170 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-26-546T>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435814 | |||||||
| chr7:99435866 | C | A | 1 | a0001c0002t0031g0208 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-26-598G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435866 | |||||||
| chr7:99435866 | C | T | 4 | a0001c0003t0004g0218 a0001c0003t0005g0039 a0001c0003t0005g0216 others(1): Show |
5 | HG01243.hp1 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-26-598G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435866 | |||||||
| chr7:99435934 | G | GA | 53 | a0001c0001t0001g0168 a0001c0001t0002g0234 a0001c0001t0003g0043 others(50): Show |
70 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.-26-667dupT | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435934 | |||||||
| chr7:99435945 | A | AT | 2 | a0001c0001t0008g0021 a0001c0003t0001g0215 |
4 | HG00323.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-678_-26-677ins others(1): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435945 | |||||||
| chr7:99435945 | A | T | 24 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0011g0020 others(21): Show |
32 | HG00099.hp2 HG01081.hp2 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.-26-677T>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99435945 | |||||||
| chr7:99436051 | T | G | 2 | a0001c0014t0016g0246 a0001c0014t0035g0245 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-26-783A>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99436051 | |||||||
| chr7:99436132 | C | T | 1 | a0001c0001t0011g0020 | 3 | HG02970.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-26-864G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99436132 | |||||||
| chr7:99436432 | G | A | 31 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(28): Show |
44 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.-26-1164C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99436432 | |||||||
| chr7:99436453 | G | A | 54 | a0001c0002t0001g0188 a0001c0002t0002g0002 a0001c0002t0002g0003 others(51): Show |
90 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-26-1185C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99436453 | |||||||
| chr7:99436616 | AAAC | A | 4 | a0004c0007t0008g0238 a0004c0007t0008g0239 a0004c0007t0008g0240 others(1): Show |
4 | HG01081.hp2 HG01891.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-1351_-26-1349d others(5): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99436616 | |||||||
| chr7:99436713 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-26-1445C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99436713 | |||||||
| chr7:99436844 | G | A | 2 | a0001c0014t0016g0246 a0001c0014t0035g0245 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-26-1576C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99436844 | |||||||
| chr7:99437009 | T | C | 2 | a0003c0006t0004g0010 a0003c0006t0004g0247 |
5 | HG02572.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+1683A>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99437009 | |||||||
| chr7:99437072 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-27+1620C>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99437072 | |||||||
| chr7:99437108 | C | G | 1 | a0001c0008t0007g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-27+1584G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99437108 | |||||||
| chr7:99437310 | ATTTCT | A | 3 | a0001c0001t0001g0212 a0001c0002t0014g0213 a0001c0002t0014g0214 |
3 | HG02895.hp1 HG02897.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-27+1377_-27+1381d others(7): Show |
PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99437310 | |||||||
| chr7:99437451 | C | T | 1 | a0001c0001t0006g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-27+1241G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99437451 | |||||||
| chr7:99437545 | C | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0051 |
4 | NA18944.hp2 NA18979.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+1147G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99437545 | |||||||
| chr7:99437588 | C | A | 31 | a0001c0001t0002g0234 a0001c0001t0003g0043 a0001c0001t0003g0235 others(28): Show |
44 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.-27+1104G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99437588 | |||||||
| chr7:99437643 | C | A | 3 | a0004c0007t0008g0238 a0004c0007t0008g0239 a0004c0007t0008g0240 |
3 | HG01081.hp2 HG01891.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-27+1049G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99437643 | |||||||
| chr7:99437739 | A | C | 2 | a0003c0006t0004g0010 a0003c0006t0004g0247 |
5 | HG02572.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+953T>G | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99437739 | |||||||
| chr7:99438081 | G | A | 4 | a0001c0001t0005g0242 a0001c0001t0005g0243 a0001c0001t0011g0020 others(1): Show |
6 | HG02258.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27+611C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99438081 | |||||||
| chr7:99438116 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-27+576G>A | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99438116 | |||||||
| chr7:99438508 | C | A | 3 | a0001c0014t0016g0246 a0001c0014t0035g0245 a0001c0017t0016g0244 |
3 | HG02647.hp2 HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-27+184G>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99438508 | |||||||
| chr7:99438634 | C | G | 1 | a0001c0001t0001g0048 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-27+58G>C | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99438634 | |||||||
| chr7:99438660 | G | A | 3 | a0001c0001t0008g0021 a0003c0006t0004g0010 a0003c0006t0004g0247 |
8 | HG02451.hp1 HG02572.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27+32C>T | PTCD1 | ENSG00000106246.18 | transcript | ENST00000292478.9 | protein_coding | 1/7 | chr7 | 99438660 |