Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7512 |
| ensemblid | ENSG00000122121.12 |
| hgncid | 12823 |
| symbol | XPNPEP2 |
| name | X-prolyl aminopeptidase 2 |
| refseq_nuc | NM_003399.6 |
| refseq_prot | NP_003390.4 |
| ensembl_nuc | ENST00000371106.4 |
| ensembl_prot | ENSP00000360147.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 129738979 |
| end | 129769536 |
| strand | + |
| ver | v1.2 |
| region | chrX:129738979-129769536 |
| region5000 | chrX:129733979-129774536 |
| regionname0 | XPNPEP2_chrX_129738979_129769536 |
| regionname5000 | XPNPEP2_chrX_129733979_129774536 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 674 | 297 | 75 | 49 | 132 | 9 | 30 | 102 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | MARAH others(669): Show |
chrX | 129733979 | 129774536 |
| a0002 | 0/0 | 674 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | MARAH others(669): Show |
chrX | 129733979 | 129774536 |
| a0003 | 0/0 | 674 | 3 | 0 | 0 | 2 | 0 | 1 | 2 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | MARAH others(669): Show |
chrX | 129733979 | 129774536 |
| a0004 | 0/0 | 674 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | MARAH others(669): Show |
chrX | 129733979 | 129774536 |
| a0005 | 0/0 | 674 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | MARAH others(669): Show |
chrX | 129733979 | 129774536 |
| a0006 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | MARAH others(669): Show |
chrX | 129733979 | 129774536 |
| a0007 | 0/0 | 674 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | MARAH others(669): Show |
chrX | 129733979 | 129774536 |
| a0008 | 0/0 | 663 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | MARAH others(658): Show |
chrX | 129733979 | 129774536 |
| a0009 | 0/0 | 674 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | MARAH others(669): Show |
chrX | 129733979 | 129774536 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2022 | 202 | 68 | 17 | 101 | 2 | 14 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0001c0002 | 1/1 | 2022 | 90 | 6 | 31 | 30 | 6 | 15 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0001c0006 | 0/0 | 2022 | 2 | 0 | 0 | 0 | 1 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0001c0007 | 0/0 | 2022 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0001c0010 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0001c0014 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0002c0003 | 0/0 | 2022 | 3 | 2 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0003c0004 | 0/0 | 2022 | 3 | 0 | 0 | 2 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0004c0005 | 0/0 | 2022 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0005c0011 | 0/0 | 2022 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0006c0012 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0007c0013 | 0/0 | 2022 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 | ||
| a0008c0008 | 0/0 | 1989 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(1984): Show |
chrX | 129733979 | 129774536 | ||
| a0009c0009 | 0/0 | 2022 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ATGGC others(2017): Show |
chrX | 129733979 | 129774536 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3311 | 39 | 2 | 6 | 24 | 1 | 6 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0002 | 0/0 | 3311 | 51 | 22 | 7 | 16 | 0 | 6 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0003 | 0/0 | 3311 | 44 | 8 | 0 | 34 | 0 | 2 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0004 | 0/0 | 3311 | 23 | 3 | 1 | 19 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0005 | 0/0 | 3311 | 13 | 13 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0006 | 0/0 | 3311 | 4 | 2 | 1 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0007 | 0/0 | 3311 | 5 | 5 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0008 | 0/0 | 3311 | 6 | 4 | 2 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0009 | 0/0 | 3311 | 4 | 4 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0010 | 0/0 | 3311 | 3 | 0 | 0 | 3 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0011 | 0/0 | 3311 | 3 | 3 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0012 | 0/0 | 3311 | 3 | 0 | 0 | 3 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0015 | 0/0 | 3311 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0017 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0018 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0001t0019 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0002t0001 | 1/1 | 3311 | 85 | 3 | 31 | 29 | 6 | 14 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0002t0002 | 0/0 | 3311 | 4 | 3 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0002t0016 | 0/0 | 3311 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0006t0001 | 0/0 | 3311 | 2 | 0 | 0 | 0 | 1 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0007t0002 | 0/0 | 3311 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0010t0005 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0001c0014t0013 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0002c0003t0002 | 0/0 | 3311 | 2 | 1 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0002c0003t0005 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0003c0004t0006 | 0/0 | 3311 | 3 | 0 | 0 | 2 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0004c0005t0007 | 0/0 | 3311 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0005c0011t0001 | 0/0 | 3311 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0006c0012t0001 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0007c0013t0014 | 0/0 | 3311 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| a0008c0008t0003 | 0/0 | 3278 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3273): Show |
chrX | 129733979 | 129774536 |
| a0009c0009t0006 | 0/0 | 3311 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | ACAGT others(3306): Show |
chrX | 129733979 | 129774536 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0006g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0007g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0007g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0007g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0008g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0009g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0009g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0010g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0010g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0010g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0011g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0011g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0012g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0012g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0015g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0017g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0001t0019g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0003 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0237 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0002t0016g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0006t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0006t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0007t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0010t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0001c0014t0013g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0002c0003t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0002c0003t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0002c0003t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0003c0004t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0003c0004t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0003c0004t0006g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0004c0005t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0004c0005t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0005c0011t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0006c0012t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0007c0013t0014g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0008c0008t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| a0009c0009t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | GBR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0110 | EUR | GBR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | GBR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0233 | EUR | FIN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00323 | hp1 | a0001 | c0006 | t0001 | g0111 | EUR | FIN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0270 | EUR | FIN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0159 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0273 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0258 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0206 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0268 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01081 | hp1 | a0001 | c0007 | t0002 | g0014 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0262 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0229 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0063 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0202 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0214 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0235 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0249 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01243 | hp1 | a0002 | c0003 | t0002 | g0292 | AMR | PUR | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0261 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0088 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0251 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0193 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0204 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0257 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0230 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0226 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0293 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0255 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0207 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0259 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | CDX | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | CDX | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0015 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02258 | hp1 | a0004 | c0005 | t0007 | g0007 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02280 | hp1 | a0001 | c0010 | t0005 | g0213 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0260 | AMR | PEL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0294 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0199 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0034 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0269 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0211 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0185 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0285 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0284 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0192 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0286 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0221 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0250 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0220 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0282 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02970 | hp2 | a0001 | c0001 | t0008 | g0201 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02976 | hp1 | a0002 | c0003 | t0005 | g0217 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0266 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0238 | AFR | GWD | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0299 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0287 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0013 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0244 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0291 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0272 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0239 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03516 | hp2 | a0004 | c0005 | t0007 | g0283 | AFR | ESN | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03669 | hp1 | a0001 | c0006 | t0001 | g0143 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03669 | hp2 | a0001 | c0002 | t0016 | g0246 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | STU | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0263 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0267 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0264 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0232 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0228 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | STU | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0274 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04184 | hp2 | a0003 | c0004 | t0006 | g0279 | SAS | BEB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04199 | hp1 | a0005 | c0011 | t0001 | g0252 | SAS | STU | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0219 | SAS | STU | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | YRI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CHB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | YRI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | YRI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18947 | hp1 | a0001 | c0001 | t0012 | g0177 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18959 | hp1 | a0006 | c0012 | t0001 | g0102 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18975 | hp1 | a0003 | c0004 | t0006 | g0135 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18997 | hp2 | a0001 | c0001 | t0010 | g0170 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18999 | hp2 | a0001 | c0001 | t0012 | g0172 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0281 | AFR | LWK | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19030 | hp2 | a0001 | c0001 | t0011 | g0008 | AFR | LWK | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0288 | AFR | LWK | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19056 | hp1 | a0001 | c0001 | t0010 | g0134 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19057 | hp1 | a0007 | c0013 | t0014 | g0144 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19059 | hp1 | a0001 | c0014 | t0013 | g0017 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19065 | hp2 | a0001 | c0001 | t0006 | g0130 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19072 | hp1 | a0003 | c0004 | t0006 | g0096 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19074 | hp2 | a0001 | c0001 | t0019 | g0222 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19075 | hp1 | a0008 | c0008 | t0003 | g0009 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19081 | hp1 | a0001 | c0001 | t0012 | g0242 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19089 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19090 | hp1 | a0001 | c0001 | t0010 | g0152 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | YRI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0008 | AFR | ASW | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | ASW | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0003 | EUR | TSI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20805 | hp1 | a0001 | c0001 | t0015 | g0223 | EUR | TSI | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | GIH | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0195 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0265 | AMR | CLM | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0208 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02486 | hp1 | a0001 | c0001 | t0018 | g0209 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0290 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | ACB | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG03471 | hp1 | a0002 | c0003 | t0002 | g0289 | AFR | MSL | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | USA | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0302 | AFR | USA | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | USA | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | USA | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA21309 | hp1 | a0009 | c0009 | t0006 | g0190 | AFR | LWK | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | LWK | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0237 | REF | REF | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0003 | REF | REF | XPNPEP2_chrX_129733979_129774536 | XPNPEP2 | chrX | 129733979 | 129774536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:129744028 | A | G | 1 | a0003 | 3 | HG04184.hp2 NA18975.hp1 NA19072.hp1 |
missense_variant | MODERATE | c.191A>G | p.Gln64Arg | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/21 | 426/3311 | 191/2025 | 64/674 | chrX | 129744028 | |||
| chrX:129745233 | C | T | 1 | a0007 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.265C>T | p.Arg89Cys | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/21 | 500/3311 | 265/2025 | 89/674 | chrX | 129745233 | |||
| chrX:129751759 | C | G | 1 | a0004 | 2 | HG02258.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.754C>G | p.Arg252Gly | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/21 | 989/3311 | 754/2025 | 252/674 | chrX | 129751759 | |||
| chrX:129752254 | G | A | 1 | a0005 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.926G>A | p.Arg309His | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1161/3311 | 926/2025 | 309/674 | chrX | 129752254 | |||
| chrX:129754518 | A | G | 1 | a0009 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1154A>G | p.Lys385Arg | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/21 | 1389/3311 | 1154/2025 | 385/674 | chrX | 129754518 | |||
| chrX:129754551 | C | T | 1 | a0002 | 3 | HG01243.hp1 HG02976.hp1 HG03471.hp1 |
missense_variant | MODERATE | c.1187C>T | p.Ser396Leu | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/21 | 1422/3311 | 1187/2025 | 396/674 | chrX | 129754551 | |||
| chrX:129756546 | G | A | 1 | a0006 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1358G>A | p.Gly453Glu | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/21 | 1593/3311 | 1358/2025 | 453/674 | chrX | 129756546 | |||
| chrX:129760498 | CCTCTCCC others(39): Show |
C | 1 | a0008 | 1 | NA19075.hp1 | splice_acceptor_variant&conservative_inframe_deletion&splice_region_variant&intron_variant | HIGH | c.1429-13_1461delCTC others(43): Show |
p.Glu477_Asp488del | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/21 | 1429/2025 | 477/674 | chrX | 129760498 | ||||
| chrX:129760563 | T | C | 1 | a0008 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.1480T>C | p.Phe494Leu | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/21 | 1715/3311 | 1480/2025 | 494/674 | chrX | 129760563 | |||
| chrX:129769534 | A | G | 1 | a0001 | 3 | NA18997.hp2 NA19056.hp1 NA19090.hp1 |
splice_region_variant | LOW | c.*1049A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | chrX | 129769534 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:129742136 | G | T | 1 | a0001c0014 | 1 | NA19059.hp1 | synonymous_variant | LOW | c.78G>T | p.Val26Val | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/21 | 313/3311 | 78/2025 | 26/674 | chrX | 129742136 | |||
| chrX:129746638 | T | C | 10 | a0001c0001 a0001c0007 a0001c0010 others(7): Show |
216 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(213): Show |
synonymous_variant | LOW | c.447T>C | p.Pro149Pro | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/21 | 682/3311 | 447/2025 | 149/674 | chrX | 129746638 | |||
| chrX:129752174 | T | C | 1 | a0001c0007 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.846T>C | p.Phe282Phe | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1081/3311 | 846/2025 | 282/674 | chrX | 129752174 | |||
| chrX:129752201 | C | T | 1 | a0001c0010 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.873C>T | p.Asn291Asn | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/21 | 1108/3311 | 873/2025 | 291/674 | chrX | 129752201 | |||
| chrX:129762728 | C | A | 1 | a0008c0008 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.1698C>A | p.Ile566Ile | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/21 | 1933/3311 | 1698/2025 | 566/674 | chrX | 129762728 | |||
| chrX:129767686 | C | G | 1 | a0001c0006 | 2 | HG00323.hp1 HG03669.hp1 |
synonymous_variant | LOW | c.1824C>G | p.Pro608Pro | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/21 | 2059/3311 | 1824/2025 | 608/674 | chrX | 129767686 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:129739079 | C | T | 1 | a0001c0001t0019 | 1 | NA19074.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-135C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | chrX | 129739079 | |||||||
| chrX:129739104 | A | G | 1 | a0001c0001t0018 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 110 | chrX | 129739104 | ||||||
| chrX:129739124 | C | T | 3 | a0001c0001t0007 a0001c0001t0017 a0004c0005t0007 |
8 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-90C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 90 | chrX | 129739124 | ||||||
| chrX:129739181 | T | C | 1 | a0001c0014t0013 | 1 | NA19059.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/21 | 33 | chrX | 129739181 | ||||||
| chrX:129768648 | C | A | 10 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(7): Show |
92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*163C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 163 | chrX | 129768648 | ||||||
| chrX:129768656 | A | G | 1 | a0007c0013t0014 | 1 | NA19057.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 171 | chrX | 129768656 | ||||||
| chrX:129768716 | C | G | 1 | a0001c0001t0008 | 6 | HG01167.hp1 HG01169.hp1 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*231C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 231 | chrX | 129768716 | ||||||
| chrX:129768817 | G | A | 3 | a0001c0001t0007 a0001c0001t0009 a0004c0005t0007 |
11 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*332G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 332 | chrX | 129768817 | ||||||
| chrX:129768887 | G | A | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(22): Show |
178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*402G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 402 | chrX | 129768887 | ||||||
| chrX:129768919 | C | T | 8 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0015 others(5): Show |
56 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*434C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 434 | chrX | 129768919 | ||||||
| chrX:129768922 | A | G | 1 | a0001c0001t0011 | 3 | HG06807.hp2 NA19030.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*437A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 437 | chrX | 129768922 | ||||||
| chrX:129769123 | C | A | 1 | a0001c0001t0015 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*638C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 638 | chrX | 129769123 | ||||||
| chrX:129769128 | G | A | 1 | a0001c0001t0012 | 3 | NA18947.hp1 NA18999.hp2 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*643G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 643 | chrX | 129769128 | ||||||
| chrX:129769275 | T | C | 1 | a0001c0002t0016 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*790T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 790 | chrX | 129769275 | ||||||
| chrX:129769496 | G | T | 3 | a0001c0001t0004 a0001c0014t0013 a0007c0013t0014 |
25 | HG01106.hp1 HG02083.hp1 HG02155.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1011G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 21/21 | 1011 | chrX | 129769496 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:129739267 | GTGCATCC others(6): Show |
G | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.49+6_49+18delTGCAT others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739267 | |||||||
| chrX:129739348 | G | C | 1 | a0001c0001t0003g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.49+86G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739348 | |||||||
| chrX:129739453 | C | G | 6 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0003g0298 others(3): Show |
7 | HG02647.hp1 HG03098.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+191C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739453 | |||||||
| chrX:129739471 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.49+209A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739471 | |||||||
| chrX:129739491 | C | T | 1 | a0001c0002t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.49+229C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739491 | |||||||
| chrX:129739751 | C | A | 3 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 |
3 | HG02630.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.49+489C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739751 | |||||||
| chrX:129739949 | C | G | 1 | a0001c0001t0004g0296 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.49+687C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739949 | |||||||
| chrX:129739982 | A | C | 2 | a0001c0002t0001g0294 a0001c0002t0001g0295 |
2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.49+720A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129739982 | |||||||
| chrX:129740004 | G | A | 2 | a0001c0001t0005g0015 a0001c0007t0002g0014 |
2 | HG01081.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.49+742G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740004 | |||||||
| chrX:129740083 | C | G | 1 | a0001c0002t0001g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.49+821C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740083 | |||||||
| chrX:129740353 | G | A | 89 | a0001c0001t0001g0066 a0001c0001t0001g0075 a0001c0001t0002g0018 others(86): Show |
90 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.49+1091G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740353 | |||||||
| chrX:129740402 | G | C | 6 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0003g0298 others(3): Show |
7 | HG02647.hp1 HG03098.hp1 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+1140G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740402 | |||||||
| chrX:129740438 | C | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(98): Show |
102 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.49+1176C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740438 | |||||||
| chrX:129740462 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(102): Show |
106 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.49+1200A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740462 | |||||||
| chrX:129740471 | A | G | 5 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0004g0299 others(2): Show |
6 | HG02647.hp1 HG03098.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+1209A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740471 | |||||||
| chrX:129740500 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.49+1238G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740500 | |||||||
| chrX:129740522 | G | C | 1 | a0009c0009t0006g0190 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49+1260G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740522 | |||||||
| chrX:129740523 | G | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(102): Show |
106 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.49+1261G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740523 | |||||||
| chrX:129740526 | G | C | 1 | a0001c0002t0001g0191 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.49+1264G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740526 | |||||||
| chrX:129740553 | C | G | 8 | a0001c0001t0007g0007 a0001c0001t0007g0284 a0001c0001t0007g0285 others(5): Show |
8 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+1291C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740553 | |||||||
| chrX:129740628 | C | CA | 41 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0212 others(38): Show |
42 | HG00741.hp2 HG01109.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.49+1380dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740628 | ||||||
| chrX:129740902 | A | C | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1206A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740902 | |||||||
| chrX:129740909 | T | C | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.50-1199T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740909 | |||||||
| chrX:129740939 | C | CA | 6 | a0001c0001t0001g0094 a0001c0001t0002g0018 a0001c0001t0003g0098 others(3): Show |
6 | HG04228.hp1 NA18939.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-1155dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740939 | ||||||
| chrX:129740956 | A | AG | 133 | a0001c0001t0001g0066 a0001c0001t0001g0075 a0001c0001t0001g0151 others(130): Show |
136 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.50-1145dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129740956 | ||||||
| chrX:129740964 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.50-1144C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740964 | |||||||
| chrX:129740988 | A | C | 1 | a0001c0002t0001g0248 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.50-1120A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129740988 | |||||||
| chrX:129741083 | C | A | 1 | a0001c0001t0008g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.50-1025C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741083 | |||||||
| chrX:129741172 | T | TG | 59 | a0001c0001t0002g0051 a0001c0001t0002g0053 a0001c0001t0002g0055 others(56): Show |
60 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.50-927dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741172 | ||||||
| chrX:129741172 | T | TGG | 121 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(118): Show |
122 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.50-928_50-927dupGG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741172 | ||||||
| chrX:129741172 | TG | T | 30 | a0001c0001t0001g0212 a0001c0001t0002g0194 a0001c0001t0002g0197 others(27): Show |
30 | HG01109.hp1 HG01123.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.50-927delG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chrX | 129741172 | ||||||
| chrX:129741174 | G | T | 1 | a0001c0002t0001g0247 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.50-934G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741174 | |||||||
| chrX:129741240 | A | G | 1 | a0001c0002t0001g0219 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.50-868A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741240 | |||||||
| chrX:129741245 | C | T | 1 | a0001c0002t0001g0280 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.50-863C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741245 | |||||||
| chrX:129741505 | T | A | 1 | a0001c0002t0001g0249 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.50-603T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741505 | |||||||
| chrX:129741692 | T | A | 1 | a0001c0001t0002g0194 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.50-416T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741692 | |||||||
| chrX:129741737 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.50-371G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741737 | |||||||
| chrX:129741794 | A | G | 19 | a0001c0001t0002g0198 a0001c0001t0002g0200 a0001c0001t0002g0205 others(16): Show |
20 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.50-314A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741794 | |||||||
| chrX:129741825 | C | T | 83 | a0001c0001t0001g0075 a0001c0001t0001g0184 a0001c0001t0002g0018 others(80): Show |
83 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.50-283C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741825 | |||||||
| chrX:129741962 | G | T | 3 | a0001c0001t0002g0205 a0001c0001t0002g0216 a0002c0003t0005g0217 |
3 | HG02896.hp2 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.50-146G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129741962 | |||||||
| chrX:129742002 | G | A | 124 | a0001c0001t0001g0151 a0001c0001t0001g0184 a0001c0001t0002g0018 others(121): Show |
126 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.50-106G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129742002 | |||||||
| chrX:129742050 | C | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0186 a0001c0001t0009g0204 |
3 | HG01891.hp2 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.50-58C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129742050 | |||||||
| chrX:129742098 | C | T | 1 | a0001c0001t0006g0195 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.50-10C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 1/20 | chrX | 129742098 | |||||||
| chrX:129742210 | C | G | 1 | a0001c0001t0002g0036 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.123+29C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742210 | |||||||
| chrX:129742227 | A | AC | 14 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0182 others(11): Show |
14 | HG00544.hp2 HG00597.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.123+53dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742227 | ||||||
| chrX:129742246 | A | G | 2 | a0001c0001t0003g0059 a0001c0001t0006g0195 |
2 | HG01123.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.123+65A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742246 | |||||||
| chrX:129742266 | A | AC | 7 | a0001c0001t0002g0101 a0001c0001t0003g0098 a0001c0001t0004g0079 others(4): Show |
7 | HG01192.hp1 HG01243.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.123+90dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742266 | ||||||
| chrX:129742269 | CCCGCCCT others(64): Show |
C | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0147 |
3 | HG02523.hp2 NA18999.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.123+91_123+161delG others(70): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742269 | ||||||
| chrX:129742272 | G | C | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+91G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742272 | |||||||
| chrX:129742362 | C | G | 1 | a0001c0002t0001g0137 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.123+181C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742362 | |||||||
| chrX:129742373 | T | C | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+192T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742373 | |||||||
| chrX:129742374 | C | T | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+193C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742374 | |||||||
| chrX:129742580 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.123+399G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742580 | |||||||
| chrX:129742585 | G | A | 14 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(11): Show |
14 | HG00673.hp1 HG01496.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.123+404G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742585 | |||||||
| chrX:129742624 | G | A | 55 | a0001c0001t0001g0184 a0001c0001t0002g0051 a0001c0001t0002g0053 others(52): Show |
55 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.123+443G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742624 | |||||||
| chrX:129742700 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.123+519G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742700 | |||||||
| chrX:129742760 | G | A | 100 | a0001c0001t0001g0184 a0001c0001t0002g0020 a0001c0001t0002g0021 others(97): Show |
101 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.123+579G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742760 | |||||||
| chrX:129742761 | G | C | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+580G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742761 | |||||||
| chrX:129742762 | C | A | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+581C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742762 | |||||||
| chrX:129742763 | A | T | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+582A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742763 | |||||||
| chrX:129742794 | C | T | 2 | a0001c0001t0002g0194 a0001c0001t0002g0200 |
2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.123+613C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742794 | |||||||
| chrX:129742805 | G | A | 5 | a0001c0001t0004g0299 a0001c0001t0008g0201 a0001c0001t0008g0202 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+624G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742805 | |||||||
| chrX:129742821 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.123+640G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742821 | |||||||
| chrX:129742874 | T | TCTGGGCG others(56): Show |
1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.123+694_123+756dup others(63): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chrX | 129742874 | ||||||
| chrX:129742917 | C | A | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+736C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742917 | |||||||
| chrX:129742918 | A | C | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.123+737A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129742918 | |||||||
| chrX:129743088 | A | G | 1 | a0001c0010t0005g0213 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.124-873A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743088 | |||||||
| chrX:129743203 | G | A | 4 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0011g0008 others(1): Show |
5 | HG02647.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-758G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743203 | |||||||
| chrX:129743239 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.124-722G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743239 | |||||||
| chrX:129743284 | T | C | 1 | a0001c0001t0001g0075 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.124-677T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743284 | |||||||
| chrX:129743347 | A | G | 82 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0093 others(79): Show |
83 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.124-614A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743347 | |||||||
| chrX:129743481 | C | T | 5 | a0001c0001t0004g0299 a0001c0001t0008g0201 a0001c0001t0008g0202 others(2): Show |
5 | HG01167.hp1 HG01169.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124-480C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743481 | |||||||
| chrX:129743514 | C | T | 4 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.124-447C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743514 | |||||||
| chrX:129743629 | G | A | 1 | a0001c0001t0002g0024 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.124-332G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743629 | |||||||
| chrX:129743630 | C | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0094 others(44): Show |
48 | HG00544.hp2 HG00621.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.124-331C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743630 | |||||||
| chrX:129743675 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.124-286C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 2/20 | chrX | 129743675 | |||||||
| chrX:129744081 | A | T | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.234+10A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744081 | |||||||
| chrX:129744295 | A | C | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.234+224A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744295 | |||||||
| chrX:129744296 | C | T | 2 | a0002c0003t0002g0289 a0002c0003t0002g0292 |
2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.234+225C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744296 | |||||||
| chrX:129744442 | C | T | 1 | a0001c0001t0003g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.234+371C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744442 | |||||||
| chrX:129744456 | A | C | 84 | a0001c0001t0001g0184 a0001c0001t0002g0020 a0001c0001t0002g0021 others(81): Show |
85 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.234+385A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744456 | |||||||
| chrX:129744497 | C | T | 1 | a0001c0001t0003g0052 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.234+426C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744497 | |||||||
| chrX:129744518 | G | A | 1 | a0001c0001t0006g0195 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.234+447G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744518 | |||||||
| chrX:129744861 | C | T | 3 | a0001c0001t0002g0205 a0001c0001t0002g0216 a0002c0003t0005g0217 |
3 | HG02896.hp2 HG02897.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.235-342C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744861 | |||||||
| chrX:129744940 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0093 others(77): Show |
81 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.235-263C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129744940 | |||||||
| chrX:129745052 | G | A | 1 | a0001c0002t0001g0161 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.235-151G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129745052 | |||||||
| chrX:129745072 | G | A | 2 | a0001c0001t0004g0062 a0001c0001t0004g0063 |
2 | HG01106.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.235-131G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129745072 | |||||||
| chrX:129745168 | G | A | 8 | a0001c0001t0002g0227 a0001c0002t0001g0005 a0001c0002t0001g0109 others(5): Show |
9 | HG01975.hp1 HG02015.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.235-35G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 3/20 | chrX | 129745168 | |||||||
| chrX:129745390 | A | G | 1 | a0001c0010t0005g0213 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.298+124A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745390 | |||||||
| chrX:129745411 | C | T | 1 | a0001c0001t0004g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.298+145C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745411 | |||||||
| chrX:129745412 | AC | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0166 a0008c0008t0003g0009 |
3 | NA19059.hp2 NA19067.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.298+150delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chrX | 129745412 | ||||||
| chrX:129745516 | C | T | 6 | a0001c0001t0004g0299 a0001c0001t0008g0201 a0001c0001t0008g0202 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+250C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745516 | |||||||
| chrX:129745551 | G | A | 1 | a0001c0010t0005g0213 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.298+285G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745551 | |||||||
| chrX:129745594 | C | T | 2 | a0001c0002t0001g0294 a0001c0002t0001g0295 |
2 | HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.298+328C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745594 | |||||||
| chrX:129745679 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(71): Show |
75 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.298+413C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745679 | |||||||
| chrX:129745680 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(214): Show |
220 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.298+414A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745680 | |||||||
| chrX:129745740 | C | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(65): Show |
69 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.298+474C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745740 | |||||||
| chrX:129745933 | C | A | 1 | a0001c0001t0017g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.299-303C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745933 | |||||||
| chrX:129745959 | G | A | 2 | a0001c0001t0015g0223 a0001c0002t0001g0099 |
2 | NA19074.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.299-277G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129745959 | |||||||
| chrX:129746132 | C | G | 2 | a0001c0001t0001g0181 a0001c0001t0002g0078 |
2 | NA19003.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.299-104C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129746132 | |||||||
| chrX:129746230 | C | T | 1 | a0001c0007t0002g0014 | 1 | HG01081.hp1 | splice_region_variant&intron_variant | LOW | c.299-6C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 4/20 | chrX | 129746230 | |||||||
| chrX:129746414 | G | A | 64 | a0001c0001t0001g0184 a0001c0001t0003g0010 a0001c0001t0003g0016 others(61): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.403+74G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 5/20 | chrX | 129746414 | |||||||
| chrX:129746869 | T | G | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.490+188T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129746869 | |||||||
| chrX:129747016 | A | G | 1 | a0001c0001t0004g0037 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.490+335A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129747016 | |||||||
| chrX:129747066 | A | AGGGTCAA others(9): Show |
1 | a0001c0001t0001g0140 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.490+387_490+402dup others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747066 | ||||||
| chrX:129747209 | GTGCTTTA others(13): Show |
G | 1 | a0001c0002t0001g0224 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.491-394_491-375del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chrX | 129747209 | ||||||
| chrX:129747490 | C | T | 2 | a0001c0002t0001g0239 a0001c0002t0001g0275 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.491-117C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129747490 | |||||||
| chrX:129747518 | A | G | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.491-89A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129747518 | |||||||
| chrX:129747538 | G | A | 10 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0024 others(7): Show |
10 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.491-69G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 6/20 | chrX | 129747538 | |||||||
| chrX:129747878 | C | G | 1 | a0001c0001t0009g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.637+125C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129747878 | |||||||
| chrX:129747993 | A | T | 1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.637+240A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129747993 | |||||||
| chrX:129748064 | AC | A | 3 | a0001c0001t0003g0060 a0001c0001t0003g0085 a0001c0001t0019g0222 |
3 | HG00597.hp2 NA18957.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.637+315delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748064 | ||||||
| chrX:129748331 | G | A | 1 | a0001c0001t0003g0025 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.637+578G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748331 | |||||||
| chrX:129748348 | C | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(76): Show |
80 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.637+595C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748348 | |||||||
| chrX:129748431 | C | T | 1 | a0001c0007t0002g0014 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.637+678C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748431 | |||||||
| chrX:129748530 | T | TCCGCATG others(31): Show |
1 | a0001c0001t0003g0098 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.637+778_637+815dup others(38): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129748530 | ||||||
| chrX:129748865 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.637+1112G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748865 | |||||||
| chrX:129748900 | G | A | 1 | a0001c0001t0015g0223 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.637+1147G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129748900 | |||||||
| chrX:129749033 | C | T | 35 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(32): Show |
36 | HG00673.hp1 HG01346.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.637+1280C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749033 | |||||||
| chrX:129749046 | A | G | 1 | a0001c0002t0001g0274 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.637+1293A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749046 | |||||||
| chrX:129749224 | T | C | 3 | a0001c0001t0002g0117 a0001c0001t0002g0197 a0001c0001t0002g0215 |
3 | HG01109.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.638-1244T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749224 | |||||||
| chrX:129749272 | T | C | 1 | a0001c0007t0002g0014 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.638-1196T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749272 | |||||||
| chrX:129749279 | T | A | 1 | a0001c0001t0003g0060 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.638-1189T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749279 | |||||||
| chrX:129749302 | G | A | 7 | a0001c0001t0005g0002 a0001c0001t0005g0192 a0001c0001t0005g0193 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-1166G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749302 | |||||||
| chrX:129749322 | C | T | 3 | a0001c0001t0002g0053 a0001c0001t0002g0136 a0001c0001t0002g0180 |
3 | HG02735.hp1 HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.638-1146C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749322 | |||||||
| chrX:129749378 | A | G | 1 | a0001c0001t0003g0092 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.638-1090A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749378 | |||||||
| chrX:129749387 | A | T | 1 | a0001c0001t0002g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.638-1081A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749387 | |||||||
| chrX:129749502 | G | T | 4 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0011g0008 others(1): Show |
5 | HG02647.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-966G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749502 | |||||||
| chrX:129749688 | AGATATAA others(13): Show |
A | 1 | a0001c0001t0001g0097 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.638-777_638-758del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chrX | 129749688 | ||||||
| chrX:129749753 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(132): Show |
137 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(134): Show |
intron_variant | MODIFIER | c.638-715G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749753 | |||||||
| chrX:129749945 | G | A | 6 | a0001c0001t0004g0299 a0001c0001t0008g0201 a0001c0001t0008g0202 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-523G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129749945 | |||||||
| chrX:129750017 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.638-451C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750017 | |||||||
| chrX:129750122 | G | T | 1 | a0001c0001t0009g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.638-346G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750122 | |||||||
| chrX:129750178 | T | C | 11 | a0001c0001t0004g0299 a0001c0001t0005g0011 a0001c0001t0005g0012 others(8): Show |
11 | HG01167.hp1 HG01169.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.638-290T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750178 | |||||||
| chrX:129750179 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(77): Show |
81 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.638-289G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750179 | |||||||
| chrX:129750284 | G | C | 7 | a0001c0001t0005g0002 a0001c0001t0005g0192 a0001c0001t0005g0193 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.638-184G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750284 | |||||||
| chrX:129750313 | A | C | 1 | a0001c0001t0003g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.638-155A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750313 | |||||||
| chrX:129750356 | C | T | 54 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(51): Show |
55 | HG00673.hp1 HG01123.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.638-112C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750356 | |||||||
| chrX:129750411 | C | T | 3 | a0001c0002t0001g0273 a0001c0002t0002g0220 a0001c0002t0002g0238 |
3 | HG00639.hp2 HG02922.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.638-57C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 7/20 | chrX | 129750411 | |||||||
| chrX:129750631 | G | A | 3 | a0001c0001t0009g0288 a0002c0003t0002g0289 a0002c0003t0002g0292 |
3 | HG01243.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.739+62G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129750631 | |||||||
| chrX:129750737 | G | T | 1 | a0001c0007t0002g0014 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.739+168G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129750737 | |||||||
| chrX:129750739 | A | C | 5 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.739+170A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129750739 | |||||||
| chrX:129750838 | T | C | 1 | a0001c0001t0003g0086 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.739+269T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129750838 | |||||||
| chrX:129751099 | C | T | 1 | a0001c0002t0001g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.739+530C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751099 | |||||||
| chrX:129751103 | C | A | 1 | a0001c0001t0001g0166 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.739+534C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751103 | |||||||
| chrX:129751104 | A | AC | 26 | a0001c0001t0002g0021 a0001c0001t0002g0030 a0001c0001t0002g0197 others(23): Show |
27 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.739+547dupC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751104 | ||||||
| chrX:129751104 | A | C | 3 | a0001c0001t0001g0166 a0001c0001t0003g0050 a0004c0005t0007g0283 |
3 | HG03516.hp2 NA18998.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.739+535A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751104 | |||||||
| chrX:129751104 | AC | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0093 others(80): Show |
84 | HG00323.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.739+547delC | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751104 | ||||||
| chrX:129751104 | ACC | A | 44 | a0001c0001t0001g0075 a0001c0001t0001g0094 a0001c0001t0001g0118 others(41): Show |
44 | HG00544.hp2 HG00639.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.739+546_739+547del others(2): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751104 | ||||||
| chrX:129751105 | C | A | 2 | a0001c0002t0001g0248 a0004c0005t0007g0283 |
2 | HG03516.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.739+536C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751105 | |||||||
| chrX:129751106 | C | A | 1 | a0001c0002t0001g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.739+537C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751106 | |||||||
| chrX:129751109 | C | A | 2 | a0001c0001t0002g0194 a0001c0001t0002g0200 |
2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.739+540C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751109 | |||||||
| chrX:129751110 | C | A | 8 | a0001c0001t0002g0055 a0001c0001t0007g0007 a0001c0001t0007g0284 others(5): Show |
8 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.739+541C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751110 | |||||||
| chrX:129751112 | C | G | 4 | a0001c0001t0002g0205 a0001c0001t0009g0199 a0001c0002t0002g0220 others(1): Show |
4 | HG02451.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.739+543C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751112 | |||||||
| chrX:129751113 | C | A | 42 | a0001c0001t0001g0184 a0001c0001t0003g0010 a0001c0001t0003g0016 others(39): Show |
42 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.739+544C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751113 | |||||||
| chrX:129751113 | C | CA | 21 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(18): Show |
21 | HG00423.hp1 HG00423.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.739+544_739+545ins others(1): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751113 | |||||||
| chrX:129751113 | C | G | 1 | a0006c0012t0001g0102 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.739+544C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751113 | |||||||
| chrX:129751153 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(135): Show |
140 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(137): Show |
intron_variant | MODIFIER | c.739+584A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751153 | |||||||
| chrX:129751179 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(211): Show |
217 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(214): Show |
intron_variant | MODIFIER | c.740-566A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751179 | |||||||
| chrX:129751229 | C | CG | 4 | a0001c0001t0002g0101 a0001c0001t0003g0187 a0001c0001t0004g0103 others(1): Show |
4 | HG01978.hp2 HG02080.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-513dupG | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751229 | ||||||
| chrX:129751229 | C | T | 1 | a0001c0001t0018g0209 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.740-516C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751229 | |||||||
| chrX:129751295 | G | T | 1 | a0001c0001t0003g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-450G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751295 | |||||||
| chrX:129751309 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.740-436A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751309 | |||||||
| chrX:129751430 | C | A | 3 | a0001c0001t0009g0288 a0002c0003t0002g0289 a0002c0003t0002g0292 |
3 | HG01243.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.740-315C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751430 | |||||||
| chrX:129751441 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.740-304G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751441 | |||||||
| chrX:129751444 | A | C | 1 | a0001c0007t0002g0014 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.740-301A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751444 | |||||||
| chrX:129751453 | A | G | 1 | a0001c0002t0001g0109 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-292A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751453 | |||||||
| chrX:129751454 | G | A | 1 | a0001c0002t0001g0109 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-291G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751454 | |||||||
| chrX:129751511 | G | A | 1 | a0001c0001t0003g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-234G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751511 | |||||||
| chrX:129751512 | A | G | 1 | a0001c0001t0003g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-233A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751512 | |||||||
| chrX:129751523 | A | AAAAGAAA others(6): Show |
1 | a0001c0002t0001g0273 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.740-220_740-219ins others(13): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751523 | ||||||
| chrX:129751523 | A | G | 1 | a0001c0002t0001g0109 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-222A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751523 | |||||||
| chrX:129751535 | G | A | 4 | a0001c0001t0003g0187 a0001c0002t0001g0005 a0001c0002t0001g0243 others(1): Show |
4 | HG00639.hp2 HG02080.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-210G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751535 | |||||||
| chrX:129751535 | G | GAAGA | 4 | a0001c0001t0003g0114 a0001c0002t0001g0142 a0001c0002t0001g0225 others(1): Show |
4 | HG01346.hp2 HG03195.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-150_740-147dup others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | ||||||
| chrX:129751535 | G | GAAGAAAG others(5): Show |
1 | a0001c0002t0001g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.740-158_740-147dup others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | ||||||
| chrX:129751535 | G | GAAGAAAG others(9): Show |
1 | a0001c0001t0002g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.740-162_740-147dup others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | ||||||
| chrX:129751535 | GAAGA | G | 20 | a0001c0001t0002g0215 a0001c0001t0003g0043 a0001c0001t0003g0049 others(17): Show |
20 | HG00738.hp1 HG01109.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.740-150_740-147del others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | ||||||
| chrX:129751535 | GAAGAAAG others(1): Show |
G | 21 | a0001c0001t0003g0016 a0001c0001t0008g0291 a0001c0001t0015g0223 others(18): Show |
21 | HG00140.hp1 HG01071.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.740-154_740-147del others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | ||||||
| chrX:129751535 | GAAGAAAG others(5): Show |
G | 11 | a0001c0001t0003g0085 a0001c0001t0003g0157 a0001c0001t0006g0210 others(8): Show |
11 | HG00099.hp2 HG00558.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.740-158_740-147del others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | ||||||
| chrX:129751535 | GAAGAAAG others(9): Show |
G | 6 | a0001c0001t0003g0081 a0001c0001t0004g0079 a0001c0002t0001g0206 others(3): Show |
6 | HG00741.hp2 HG01975.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.740-162_740-147del others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | ||||||
| chrX:129751535 | GAAGAAAG others(13): Show |
G | 2 | a0001c0001t0002g0197 a0001c0001t0004g0089 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.740-166_740-147del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | ||||||
| chrX:129751535 | GAAGAAAG others(17): Show |
G | 4 | a0001c0001t0002g0194 a0001c0001t0002g0200 a0001c0001t0004g0299 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-170_740-147del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | ||||||
| chrX:129751535 | GAAGAAAG others(25): Show |
G | 1 | a0001c0001t0005g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.740-178_740-147del others(32): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751535 | ||||||
| chrX:129751537 | A | G | 1 | a0001c0001t0003g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-208A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751537 | |||||||
| chrX:129751538 | G | A | 1 | a0001c0001t0003g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-207G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751538 | |||||||
| chrX:129751538 | GA | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0181 a0001c0001t0002g0148 |
3 | HG03688.hp1 NA19004.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.740-204delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751538 | ||||||
| chrX:129751539 | A | G | 1 | a0001c0001t0003g0050 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.740-206A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751539 | |||||||
| chrX:129751559 | AAAGAAAG others(33): Show |
A | 3 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 |
3 | HG02630.hp2 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.740-182_740-143del others(40): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751559 | ||||||
| chrX:129751563 | AAAGAAAG others(37): Show |
A | 1 | a0001c0001t0005g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.740-178_740-135del others(44): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751563 | ||||||
| chrX:129751575 | AAAGAAAG others(17): Show |
A | 2 | a0001c0001t0004g0063 a0001c0001t0005g0192 |
2 | HG01106.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.740-166_740-143del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751575 | ||||||
| chrX:129751579 | AAAGAAAG others(13): Show |
A | 4 | a0001c0001t0005g0193 a0001c0001t0007g0284 a0001c0002t0001g0261 others(1): Show |
4 | HG01258.hp1 HG01884.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-162_740-143del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751579 | ||||||
| chrX:129751579 | AAAGAAAG others(17): Show |
A | 2 | a0001c0001t0005g0203 a0001c0001t0005g0208 |
2 | HG02109.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.740-162_740-139del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751579 | ||||||
| chrX:129751581 | AGAAAGAA others(10): Show |
A | 1 | a0001c0001t0004g0062 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.740-160_740-144del others(17): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751581 | ||||||
| chrX:129751583 | A | G | 2 | a0001c0001t0004g0183 a0007c0013t0014g0144 |
2 | HG02155.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.740-162A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751583 | |||||||
| chrX:129751583 | AAAGAAAG others(9): Show |
A | 4 | a0001c0001t0002g0205 a0001c0001t0002g0216 a0001c0001t0007g0285 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.740-158_740-143del others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751583 | ||||||
| chrX:129751583 | AAAGAAAG others(13): Show |
A | 4 | a0001c0001t0005g0002 a0001c0001t0005g0221 a0001c0001t0005g0250 others(1): Show |
4 | HG02622.hp2 HG02630.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-158_740-139del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751583 | ||||||
| chrX:129751583 | AAAGAAAG others(17): Show |
A | 2 | a0001c0001t0008g0202 a0001c0001t0008g0214 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.740-158_740-135del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751583 | ||||||
| chrX:129751583 | AAAGAAAG others(21): Show |
A | 1 | a0001c0001t0002g0175 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.740-158_740-131del others(28): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751583 | ||||||
| chrX:129751587 | A | AAAGGAAA others(6): Show |
1 | a0001c0001t0004g0042 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.740-155_740-154ins others(13): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | ||||||
| chrX:129751587 | A | AAGGAAGG others(4): Show |
1 | a0001c0001t0004g0037 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.740-157_740-156ins others(11): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | ||||||
| chrX:129751587 | A | G | 12 | a0001c0001t0001g0184 a0001c0001t0002g0197 a0001c0001t0003g0047 others(9): Show |
12 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(9): Show |
intron_variant | MODIFIER | c.740-158A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751587 | |||||||
| chrX:129751587 | AAAGAAAG others(5): Show |
A | 2 | a0001c0001t0007g0007 a0001c0002t0001g0231 |
2 | HG01175.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.740-154_740-143del others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | ||||||
| chrX:129751587 | AAAGAAAG others(13): Show |
A | 4 | a0001c0001t0002g0070 a0001c0001t0002g0095 a0001c0001t0002g0176 others(1): Show |
4 | HG01346.hp1 HG02280.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-154_740-135del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | ||||||
| chrX:129751587 | AAAGAAAG others(17): Show |
A | 2 | a0001c0001t0002g0020 a0001c0001t0003g0116 |
2 | HG00673.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.740-154_740-131del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751587 | ||||||
| chrX:129751588 | AAGAAAGA others(11): Show |
A | 1 | a0001c0001t0005g0002 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.740-156_740-139del others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751588 | |||||||
| chrX:129751591 | A | AAAGG | 4 | a0001c0001t0004g0155 a0001c0002t0001g0058 a0001c0002t0001g0064 others(1): Show |
4 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-151_740-150ins others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | ||||||
| chrX:129751591 | A | AAAGGAAG others(5): Show |
1 | a0001c0001t0004g0039 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.740-151_740-150ins others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | ||||||
| chrX:129751591 | A | G | 43 | a0001c0001t0001g0184 a0001c0001t0002g0117 a0001c0001t0002g0197 others(40): Show |
43 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.740-154A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751591 | |||||||
| chrX:129751591 | AAAGAAAG others(1): Show |
A | 7 | a0001c0001t0008g0290 a0001c0002t0001g0235 a0001c0002t0001g0249 others(4): Show |
7 | HG01169.hp2 HG01192.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.740-150_740-143del others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | ||||||
| chrX:129751591 | AAAGAAAG others(5): Show |
A | 2 | a0001c0002t0001g0230 a0002c0003t0005g0217 |
2 | HG01943.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.740-150_740-139del others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | ||||||
| chrX:129751591 | AAAGAAAG others(9): Show |
A | 3 | a0001c0001t0002g0029 a0001c0001t0002g0065 a0001c0001t0002g0069 |
3 | HG01496.hp1 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.740-150_740-135del others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | ||||||
| chrX:129751591 | AAAGAAAG others(13): Show |
A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0024 a0001c0001t0002g0091 |
3 | HG01934.hp1 NA18953.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.740-150_740-131del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | ||||||
| chrX:129751591 | AAAGAAAG others(21): Show |
A | 3 | a0001c0001t0001g0075 a0001c0001t0002g0018 a0003c0004t0006g0096 |
3 | NA18940.hp1 NA19072.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.740-150_740-123del others(28): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751591 | ||||||
| chrX:129751595 | A | AAAGAAAG others(13): Show |
1 | a0001c0006t0001g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGAAAG others(7): Show |
1 | a0001c0002t0001g0099 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGAAAG others(9): Show |
1 | a0001c0002t0001g0297 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.740-147_740-146ins others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGAAAG others(13): Show |
1 | a0001c0001t0004g0105 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGAAAG others(7): Show |
1 | a0001c0001t0003g0023 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGAAAG others(23): Show |
1 | a0001c0001t0003g0132 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(30): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGAAAG others(16): Show |
1 | a0001c0001t0003g0084 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(23): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGAAAG others(1): Show |
3 | a0001c0002t0001g0035 a0001c0002t0001g0088 a0001c0002t0001g0219 |
3 | HG00642.hp1 HG01358.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.740-147_740-146ins others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGAAAG others(5): Show |
4 | a0001c0001t0003g0158 a0001c0001t0003g0167 a0001c0001t0008g0201 others(1): Show |
4 | HG00621.hp1 HG02970.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-147_740-146ins others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGAAGA others(15): Show |
1 | a0001c0002t0001g0005 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGAAGG others(8): Show |
1 | a0001c0001t0003g0048 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.740-147_740-146ins others(15): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGG | 3 | a0001c0002t0001g0236 a0001c0002t0016g0246 a0001c0006t0001g0143 |
3 | HG01256.hp1 HG03669.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.740-105_740-102dup others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | AAAGGAAG others(5): Show |
1 | a0001c0001t0004g0106 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.740-113_740-102dup others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | A | G | 81 | a0001c0001t0001g0184 a0001c0001t0002g0055 a0001c0001t0002g0117 others(78): Show |
81 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.740-150A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751595 | |||||||
| chrX:129751595 | AAAGG | A | 7 | a0001c0001t0001g0118 a0001c0001t0001g0141 a0001c0001t0002g0036 others(4): Show |
7 | HG01255.hp1 HG02040.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.740-105_740-102del others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | AAAGGAAG others(1): Show |
A | 7 | a0001c0001t0001g0145 a0001c0001t0001g0169 a0001c0001t0001g0174 others(4): Show |
7 | HG02723.hp2 HG03239.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.740-109_740-102del others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | AAAGGAAG others(5): Show |
A | 18 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0119 others(15): Show |
18 | HG00639.hp1 HG01243.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.740-113_740-102del others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | AAAGGAAG others(9): Show |
A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0125 others(13): Show |
16 | HG01069.hp1 HG01175.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.740-117_740-102del others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | AAAGGAAG others(13): Show |
A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0123 others(12): Show |
15 | HG00408.hp2 HG00544.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.740-121_740-102del others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751595 | AAAGGAAG others(17): Show |
A | 12 | a0001c0001t0001g0121 a0001c0001t0001g0131 a0001c0001t0001g0153 others(9): Show |
13 | HG01496.hp2 HG02809.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.740-125_740-102del others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751595 | ||||||
| chrX:129751597 | AGGAAGGA others(6): Show |
A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0180 |
2 | HG02735.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.740-146_740-134del others(13): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751597 | ||||||
| chrX:129751597 | AGGAAGGA others(10): Show |
A | 2 | a0001c0001t0001g0151 a0001c0001t0009g0204 |
2 | HG01891.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.740-146_740-130del others(17): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751597 | ||||||
| chrX:129751599 | G | A | 15 | a0001c0001t0001g0097 a0001c0001t0001g0168 a0001c0001t0001g0212 others(12): Show |
15 | HG01081.hp1 HG01884.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.740-146G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751599 | |||||||
| chrX:129751602 | G | A | 1 | a0001c0001t0006g0195 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.740-143G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751602 | |||||||
| chrX:129751603 | G | A | 13 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0141 others(10): Show |
13 | HG01978.hp2 HG02040.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.740-142G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751603 | |||||||
| chrX:129751606 | G | A | 1 | a0001c0001t0006g0195 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.740-139G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751606 | |||||||
| chrX:129751606 | GGAAGGAA others(7): Show |
G | 1 | a0001c0001t0001g0212 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.740-138_740-125del others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751606 | |||||||
| chrX:129751607 | G | A | 16 | a0001c0001t0001g0118 a0001c0001t0001g0141 a0001c0001t0001g0145 others(13): Show |
16 | HG01978.hp2 HG02040.hp1 HG02723.hp2 others(13): Show |
intron_variant | MODIFIER | c.740-138G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751607 | |||||||
| chrX:129751608 | AAGGAAGG others(4): Show |
A | 1 | a0001c0001t0001g0097 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.740-135_740-125del others(11): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751608 | ||||||
| chrX:129751610 | GGAAGGAA others(3): Show |
G | 1 | a0001c0001t0001g0168 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.740-134_740-125del others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751610 | |||||||
| chrX:129751611 | G | A | 23 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0118 others(20): Show |
23 | HG00639.hp1 HG01978.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.740-134G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751611 | |||||||
| chrX:129751614 | G | A | 2 | a0001c0001t0002g0078 a0001c0001t0002g0180 |
2 | HG02735.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.740-131G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751614 | |||||||
| chrX:129751615 | G | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0093 a0001c0001t0001g0094 others(33): Show |
36 | HG00639.hp1 HG01069.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.740-130G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751615 | |||||||
| chrX:129751618 | G | A | 4 | a0001c0001t0001g0151 a0001c0001t0002g0078 a0001c0001t0002g0180 others(1): Show |
4 | HG01891.hp2 HG02735.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.740-127G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751618 | |||||||
| chrX:129751619 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0093 others(44): Show |
48 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.740-126G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751619 | |||||||
| chrX:129751622 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0212 a0001c0001t0009g0204 |
3 | HG01891.hp2 HG02148.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.740-123G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751622 | |||||||
| chrX:129751623 | G | A | 2 | a0001c0001t0002g0100 a0001c0001t0002g0186 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.740-122G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751623 | |||||||
| chrX:129751640 | A | AAGGAAGG others(9): Show |
1 | a0001c0001t0003g0104 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.740-102_740-101ins others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751640 | ||||||
| chrX:129751640 | A | AAGGAAGG others(5): Show |
1 | a0001c0001t0003g0108 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.740-102_740-101ins others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751640 | ||||||
| chrX:129751640 | A | AAGGAAGG others(1): Show |
5 | a0001c0001t0003g0010 a0001c0001t0003g0052 a0001c0001t0003g0086 others(2): Show |
5 | HG00408.hp1 HG02027.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.740-102_740-101ins others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751640 | ||||||
| chrX:129751640 | A | AAGGG | 6 | a0001c0001t0003g0025 a0001c0001t0003g0060 a0001c0001t0003g0159 others(3): Show |
6 | HG00423.hp2 HG00597.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.740-101_740-98dupG others(3): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chrX | 129751640 | ||||||
| chrX:129751640 | A | G | 28 | a0001c0001t0003g0016 a0001c0001t0003g0023 a0001c0001t0003g0027 others(25): Show |
28 | HG00423.hp1 HG00558.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.740-105A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751640 | |||||||
| chrX:129751641 | A | G | 1 | a0007c0013t0014g0144 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.740-104A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751641 | |||||||
| chrX:129751644 | G | A | 1 | a0001c0002t0001g0109 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-101G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751644 | |||||||
| chrX:129751654 | A | G | 1 | a0001c0002t0001g0109 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.740-91A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751654 | |||||||
| chrX:129751714 | A | G | 7 | a0001c0001t0005g0002 a0001c0001t0005g0192 a0001c0001t0005g0193 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.740-31A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 8/20 | chrX | 129751714 | |||||||
| chrX:129751841 | T | C | 1 | a0001c0001t0003g0187 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.821+15T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129751841 | |||||||
| chrX:129751842 | A | T | 1 | a0001c0001t0003g0187 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.821+16A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129751842 | |||||||
| chrX:129751974 | G | A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0164 |
2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.821+148G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129751974 | |||||||
| chrX:129752009 | A | G | 48 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(45): Show |
49 | HG00673.hp1 HG01081.hp1 HG01123.hp1 others(46): Show |
intron_variant | MODIFIER | c.822-141A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 9/20 | chrX | 129752009 | |||||||
| chrX:129752568 | C | T | 8 | a0001c0001t0007g0007 a0001c0001t0007g0284 a0001c0001t0007g0285 others(5): Show |
8 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1017+223C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129752568 | |||||||
| chrX:129752756 | T | C | 2 | a0001c0001t0002g0194 a0001c0001t0002g0200 |
2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1018-403T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129752756 | |||||||
| chrX:129752779 | T | C | 1 | a0001c0001t0004g0299 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1018-380T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129752779 | |||||||
| chrX:129752968 | A | C | 51 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(48): Show |
51 | HG00673.hp1 HG01081.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1018-191A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129752968 | |||||||
| chrX:129753026 | T | C | 51 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(48): Show |
51 | HG00673.hp1 HG01081.hp1 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1018-133T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129753026 | |||||||
| chrX:129753076 | A | G | 2 | a0001c0001t0004g0062 a0001c0001t0004g0063 |
2 | HG01106.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1018-83A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129753076 | |||||||
| chrX:129753105 | G | T | 1 | a0001c0001t0003g0023 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1018-54G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 10/20 | chrX | 129753105 | |||||||
| chrX:129753368 | C | T | 11 | a0001c0002t0001g0004 a0001c0002t0001g0191 a0001c0002t0001g0233 others(8): Show |
12 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(9): Show |
intron_variant | MODIFIER | c.1107+120C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129753368 | |||||||
| chrX:129753381 | G | A | 2 | a0002c0003t0002g0289 a0002c0003t0002g0292 |
2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1107+133G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129753381 | |||||||
| chrX:129753695 | G | A | 65 | a0001c0001t0001g0184 a0001c0001t0003g0010 a0001c0001t0003g0016 others(62): Show |
65 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1107+447G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129753695 | |||||||
| chrX:129754017 | TA | T | 3 | a0001c0001t0001g0184 a0001c0001t0012g0242 a0001c0002t0001g0019 |
3 | HG00558.hp2 NA18987.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1108-449delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chrX | 129754017 | ||||||
| chrX:129754076 | C | T | 33 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(30): Show |
33 | HG00673.hp1 HG01346.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.1108-396C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129754076 | |||||||
| chrX:129754274 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1108-198G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129754274 | |||||||
| chrX:129754434 | C | T | 9 | a0001c0001t0002g0055 a0001c0001t0004g0299 a0001c0001t0008g0201 others(6): Show |
9 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1108-38C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129754434 | |||||||
| chrX:129754449 | T | C | 1 | a0001c0002t0001g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1108-23T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 11/20 | chrX | 129754449 | |||||||
| chrX:129754684 | C | T | 4 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217+103C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754684 | |||||||
| chrX:129754749 | G | A | 1 | a0001c0001t0009g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1217+168G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754749 | |||||||
| chrX:129754767 | C | T | 33 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(30): Show |
33 | HG00673.hp1 HG01346.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.1217+186C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754767 | |||||||
| chrX:129754772 | G | C | 1 | a0001c0002t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1217+191G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754772 | |||||||
| chrX:129754794 | A | G | 1 | a0001c0002t0001g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1217+213A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754794 | |||||||
| chrX:129754840 | G | T | 33 | a0001c0001t0001g0075 a0001c0001t0001g0151 a0001c0001t0001g0181 others(30): Show |
34 | HG00408.hp2 HG01891.hp2 HG02004.hp2 others(31): Show |
intron_variant | MODIFIER | c.1217+259G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129754840 | |||||||
| chrX:129755215 | T | C | 1 | a0001c0001t0010g0170 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1218-79T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129755215 | |||||||
| chrX:129755235 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1218-59C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 12/20 | chrX | 129755235 | |||||||
| chrX:129755410 | G | A | 1 | a0001c0002t0001g0234 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1295+39G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129755410 | |||||||
| chrX:129755488 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0094 others(36): Show |
40 | HG00544.hp2 HG00639.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1295+117G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129755488 | |||||||
| chrX:129756021 | T | C | 1 | a0001c0002t0001g0064 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1296-463T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756021 | |||||||
| chrX:129756101 | G | A | 4 | a0001c0001t0003g0114 a0001c0001t0003g0115 a0001c0001t0003g0116 others(1): Show |
4 | HG02257.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1296-383G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756101 | |||||||
| chrX:129756132 | G | A | 1 | a0001c0002t0001g0137 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1296-352G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756132 | |||||||
| chrX:129756224 | G | A | 3 | a0001c0001t0002g0117 a0001c0001t0002g0197 a0001c0001t0002g0215 |
3 | HG01109.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1296-260G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756224 | |||||||
| chrX:129756265 | G | A | 1 | a0006c0012t0001g0102 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1296-219G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756265 | |||||||
| chrX:129756266 | A | C | 1 | a0006c0012t0001g0102 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1296-218A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756266 | |||||||
| chrX:129756272 | G | A | 1 | a0001c0001t0003g0047 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1296-212G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756272 | |||||||
| chrX:129756410 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1296-74C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756410 | |||||||
| chrX:129756417 | C | T | 1 | a0001c0010t0005g0213 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1296-67C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756417 | |||||||
| chrX:129756441 | G | A | 9 | a0001c0001t0002g0055 a0001c0001t0004g0299 a0001c0001t0008g0201 others(6): Show |
9 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1296-43G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 13/20 | chrX | 129756441 | |||||||
| chrX:129756819 | G | GT | 3 | a0001c0001t0002g0194 a0001c0001t0002g0200 a0001c0001t0003g0084 |
3 | HG02109.hp1 NA19091.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1367+270dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756819 | ||||||
| chrX:129756830 | G | GTTGT | 9 | a0001c0001t0002g0055 a0001c0001t0004g0299 a0001c0001t0008g0201 others(6): Show |
9 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367+290_1367+293d others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756830 | ||||||
| chrX:129756996 | C | CTA | 25 | a0001c0001t0001g0240 a0001c0001t0002g0117 a0001c0001t0002g0138 others(22): Show |
26 | HG00597.hp1 HG00741.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1367+468_1367+469d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | C | CTATA | 7 | a0001c0001t0001g0153 a0001c0001t0002g0197 a0001c0001t0006g0130 others(4): Show |
7 | HG02280.hp1 HG02886.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1367+466_1367+469d others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | C | CTATATAT others(5): Show |
5 | a0001c0001t0003g0048 a0001c0001t0003g0052 a0001c0001t0003g0245 others(2): Show |
5 | HG02027.hp1 NA18906.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1367+458_1367+469d others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | C | CTATATAT others(7): Show |
16 | a0001c0001t0003g0010 a0001c0001t0003g0016 a0001c0001t0003g0023 others(13): Show |
16 | HG00423.hp1 HG00423.hp2 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.1367+456_1367+469d others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | C | CTATATAT others(9): Show |
6 | a0001c0001t0003g0086 a0001c0001t0003g0090 a0001c0001t0003g0098 others(3): Show |
6 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367+454_1367+469d others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | C | CTATATAT others(11): Show |
8 | a0001c0001t0003g0047 a0001c0001t0003g0060 a0001c0001t0003g0085 others(5): Show |
8 | HG00597.hp2 HG02523.hp1 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.1367+452_1367+469d others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | C | CTATATAT others(13): Show |
2 | a0001c0001t0003g0132 a0001c0001t0004g0037 |
2 | NA18943.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1367+450_1367+469d others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | C | CTATATAT others(19): Show |
1 | a0001c0001t0003g0185 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1367+444_1367+469d others(28): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | C | CTATATAT others(21): Show |
1 | a0001c0001t0003g0044 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1367+442_1367+469d others(30): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | CTA | C | 22 | a0001c0001t0001g0166 a0001c0001t0002g0069 a0001c0001t0004g0299 others(19): Show |
23 | HG01123.hp1 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1367+468_1367+469d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | CTATA | C | 5 | a0001c0001t0002g0055 a0001c0001t0002g0300 a0001c0001t0002g0301 others(2): Show |
5 | HG01081.hp1 HG02647.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+466_1367+469d others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129756996 | CTATATA | C | 13 | a0001c0001t0003g0059 a0001c0001t0003g0115 a0001c0001t0003g0116 others(10): Show |
13 | HG01884.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+464_1367+469d others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129756996 | ||||||
| chrX:129757019 | T | C | 1 | a0001c0001t0002g0024 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1367+464T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757019 | |||||||
| chrX:129757019 | TATATAC | T | 3 | a0001c0001t0002g0070 a0001c0001t0002g0148 a0001c0001t0007g0284 |
3 | HG02280.hp2 HG02723.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1367+466_1367+471d others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757019 | ||||||
| chrX:129757021 | T | C | 29 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(26): Show |
29 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.1367+466T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757021 | |||||||
| chrX:129757023 | T | C | 39 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(36): Show |
39 | HG00673.hp1 HG01346.hp1 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.1367+468T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757023 | |||||||
| chrX:129757023 | T | TATATATA others(5): Show |
1 | a0001c0014t0013g0017 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1367+469_1367+470i others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | ||||||
| chrX:129757023 | T | TATATATA others(7): Show |
7 | a0001c0001t0001g0184 a0001c0001t0004g0039 a0001c0001t0004g0041 others(4): Show |
7 | HG00558.hp2 HG03516.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1367+469_1367+470i others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | ||||||
| chrX:129757023 | T | TATATATA others(9): Show |
1 | a0001c0001t0004g0105 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1367+469_1367+470i others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | ||||||
| chrX:129757023 | T | TATATATA others(9): Show |
4 | a0001c0001t0004g0103 a0001c0001t0004g0106 a0001c0001t0004g0155 others(1): Show |
4 | HG02083.hp1 NA18949.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+469_1367+470i others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | ||||||
| chrX:129757023 | T | TATATATA others(11): Show |
5 | a0001c0001t0003g0082 a0001c0001t0003g0187 a0001c0001t0004g0062 others(2): Show |
5 | HG01106.hp1 HG02080.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+469_1367+470i others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | ||||||
| chrX:129757023 | T | TATATATA others(13): Show |
3 | a0001c0001t0004g0040 a0001c0001t0004g0149 a0001c0001t0004g0183 |
3 | HG02155.hp1 NA18939.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1367+469_1367+470i others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | ||||||
| chrX:129757023 | T | TATATATA others(15): Show |
3 | a0001c0001t0003g0080 a0001c0001t0003g0107 a0001c0001t0003g0188 |
3 | HG02132.hp1 NA18948.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1367+469_1367+470i others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | ||||||
| chrX:129757023 | T | TATATATA others(21): Show |
1 | a0001c0001t0004g0046 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1367+469_1367+470i others(30): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757023 | ||||||
| chrX:129757025 | C | T | 1 | a0001c0001t0003g0048 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1367+470C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757025 | |||||||
| chrX:129757031 | C | CATATATA others(3): Show |
28 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(25): Show |
28 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.1367+477_1367+478i others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757031 | ||||||
| chrX:129757031 | C | T | 1 | a0001c0001t0002g0024 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1367+476C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757031 | |||||||
| chrX:129757037 | C | T | 2 | a0001c0001t0002g0300 a0001c0001t0002g0301 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1367+482C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757037 | |||||||
| chrX:129757039 | T | C | 69 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(66): Show |
69 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1367+484T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757039 | |||||||
| chrX:129757047 | T | C | 4 | a0001c0001t0003g0048 a0001c0001t0003g0107 a0001c0001t0003g0187 others(1): Show |
4 | HG02080.hp1 HG02132.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.1367+492T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757047 | |||||||
| chrX:129757047 | T | TAC | 5 | a0001c0001t0004g0103 a0001c0001t0004g0105 a0001c0001t0004g0106 others(2): Show |
5 | NA18949.hp1 NA18952.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+500_1367+501d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757047 | ||||||
| chrX:129757055 | C | T | 1 | a0001c0001t0003g0048 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1367+500C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757055 | |||||||
| chrX:129757059 | T | C | 29 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(26): Show |
29 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.1367+504T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757059 | |||||||
| chrX:129757061 | T | C | 29 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(26): Show |
29 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.1367+506T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757061 | |||||||
| chrX:129757063 | T | C | 37 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(34): Show |
37 | HG00673.hp1 HG01106.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.1367+508T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757063 | |||||||
| chrX:129757063 | T | TAC | 51 | a0001c0001t0001g0184 a0001c0001t0003g0010 a0001c0001t0003g0016 others(48): Show |
51 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1367+516_1367+517d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757063 | ||||||
| chrX:129757063 | T | TACAC | 3 | a0001c0001t0004g0034 a0001c0001t0004g0037 a0001c0001t0004g0183 |
3 | HG02155.hp1 HG02523.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1367+514_1367+517d others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757063 | ||||||
| chrX:129757073 | T | C | 92 | a0001c0001t0001g0184 a0001c0001t0002g0020 a0001c0001t0002g0021 others(89): Show |
92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1367+518T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757073 | |||||||
| chrX:129757073 | T | TACACACA others(7): Show |
2 | a0001c0001t0002g0070 a0001c0001t0007g0284 |
2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1367+524_1367+537d others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757073 | ||||||
| chrX:129757073 | T | TACACACA others(9): Show |
2 | a0001c0001t0002g0300 a0001c0001t0002g0301 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1367+522_1367+537d others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757073 | ||||||
| chrX:129757073 | T | TACACACA others(11): Show |
7 | a0001c0001t0002g0148 a0001c0001t0003g0298 a0001c0001t0005g0011 others(4): Show |
7 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1367+520_1367+537d others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757073 | ||||||
| chrX:129757073 | T | TACACACA others(15): Show |
1 | a0001c0001t0009g0199 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1367+537_1367+538i others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757073 | ||||||
| chrX:129757073 | TAC | T | 7 | a0001c0001t0005g0002 a0001c0001t0005g0192 a0001c0001t0005g0193 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1367+536_1367+537d others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757073 | ||||||
| chrX:129757090 | A | G | 1 | a0001c0002t0001g0268 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1367+535A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757090 | |||||||
| chrX:129757093 | T | C | 1 | a0001c0002t0001g0218 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1367+538T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757093 | |||||||
| chrX:129757196 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(69): Show |
74 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1367+641G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757196 | |||||||
| chrX:129757314 | C | A | 1 | a0001c0001t0001g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+759C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757314 | |||||||
| chrX:129757346 | A | G | 1 | a0001c0002t0001g0226 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1367+791A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757346 | |||||||
| chrX:129757424 | G | T | 1 | a0001c0001t0005g0160 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1367+869G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757424 | |||||||
| chrX:129757516 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(126): Show |
131 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.1367+961A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757516 | |||||||
| chrX:129757537 | G | A | 9 | a0001c0001t0002g0055 a0001c0001t0004g0299 a0001c0001t0008g0201 others(6): Show |
9 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1367+982G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757537 | |||||||
| chrX:129757727 | G | A | 41 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(38): Show |
41 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.1367+1172G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757727 | |||||||
| chrX:129757796 | G | GAAGA | 27 | a0001c0001t0001g0075 a0001c0001t0001g0240 a0001c0001t0002g0100 others(24): Show |
28 | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.1367+1302_1367+130 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757796 | G | GAAGAAAG others(1): Show |
6 | a0001c0001t0002g0178 a0001c0001t0003g0083 a0001c0001t0003g0157 others(3): Show |
6 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.1367+1298_1367+130 others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757796 | G | GAAGAAAG others(3): Show |
1 | a0001c0002t0001g0142 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1367+1242_1367+125 others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757796 | G | GAAGAAAG others(5): Show |
11 | a0001c0001t0001g0277 a0001c0001t0002g0091 a0001c0001t0002g0165 others(8): Show |
11 | HG01496.hp2 HG01934.hp1 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.1367+1294_1367+130 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757796 | G | GAAGAAAG others(13): Show |
1 | a0001c0001t0004g0154 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1367+1286_1367+130 others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757796 | G | GAAGAAAG others(17): Show |
2 | a0001c0001t0002g0301 a0001c0002t0001g0255 |
2 | HG02004.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1367+1282_1367+130 others(28): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757796 | GAAGA | G | 29 | a0001c0001t0001g0129 a0001c0001t0001g0212 a0001c0001t0002g0029 others(26): Show |
30 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1367+1302_1367+130 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757796 | GAAGAAAG others(1): Show |
G | 13 | a0001c0001t0001g0181 a0001c0001t0001g0276 a0001c0001t0002g0053 others(10): Show |
13 | HG01884.hp2 HG02257.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1367+1298_1367+130 others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757796 | GAAGAAAG others(5): Show |
G | 13 | a0001c0001t0002g0028 a0001c0001t0002g0030 a0001c0001t0002g0067 others(10): Show |
13 | HG01358.hp1 HG01975.hp2 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.1367+1294_1367+130 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757796 | GAAGAAAG others(9): Show |
G | 2 | a0001c0001t0001g0128 a0001c0001t0002g0215 |
2 | HG01109.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1367+1290_1367+130 others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757796 | GAAGAAAG others(113): Show |
G | 1 | a0001c0001t0002g0055 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1367+1288_1368-121 others(4): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757796 | ||||||
| chrX:129757800 | A | G | 1 | a0001c0001t0003g0010 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1367+1245A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757800 | |||||||
| chrX:129757804 | A | C | 1 | a0001c0001t0001g0151 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1367+1249A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757804 | |||||||
| chrX:129757826 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+1271A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757826 | |||||||
| chrX:129757827 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1367+1272G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757827 | |||||||
| chrX:129757839 | GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0002g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1367+1286_1367+129 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757839 | ||||||
| chrX:129757849 | AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0002g0227 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1367+1297_1367+130 others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757849 | ||||||
| chrX:129757856 | A | G | 3 | a0001c0001t0002g0065 a0001c0001t0002g0197 a0003c0004t0006g0279 |
3 | HG02572.hp1 HG02886.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1367+1301A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757856 | |||||||
| chrX:129757857 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1367+1302A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757857 | |||||||
| chrX:129757857 | AAGAGGGA others(1): Show |
A | 13 | a0001c0001t0002g0198 a0001c0001t0003g0107 a0001c0001t0006g0210 others(10): Show |
13 | HG00099.hp2 HG00735.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1367+1307_1368-131 others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757857 | ||||||
| chrX:129757857 | AAGAGGGA others(5): Show |
A | 5 | a0001c0001t0003g0060 a0001c0001t0003g0298 a0001c0001t0005g0203 others(2): Show |
5 | HG00597.hp2 HG02922.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+1306_1368-130 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757857 | ||||||
| chrX:129757858 | AGAGG | A | 24 | a0001c0001t0001g0097 a0001c0001t0001g0123 a0001c0001t0002g0022 others(21): Show |
24 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.1367+1307_1367+131 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757858 | ||||||
| chrX:129757859 | G | GAA | 11 | a0001c0001t0001g0066 a0001c0001t0001g0119 a0001c0001t0001g0131 others(8): Show |
11 | HG01167.hp1 HG01169.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1367+1305_1367+130 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757859 | ||||||
| chrX:129757859 | G | GAAAGAAA others(7): Show |
1 | a0001c0001t0004g0034 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1367+1305_1367+130 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757859 | ||||||
| chrX:129757860 | AGG | A | 11 | a0001c0001t0001g0094 a0001c0001t0001g0120 a0001c0001t0002g0020 others(8): Show |
11 | HG00673.hp1 HG01346.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1367+1307_1367+130 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757860 | ||||||
| chrX:129757861 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0001g0121 others(76): Show |
80 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1367+1306G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757861 | |||||||
| chrX:129757862 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0118 others(88): Show |
92 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.1367+1307G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757862 | |||||||
| chrX:129757863 | G | A | 24 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0001t0001g0119 others(21): Show |
24 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1367+1308G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757863 | |||||||
| chrX:129757865 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0097 a0001c0001t0001g0118 others(78): Show |
83 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1367+1310G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757865 | |||||||
| chrX:129757866 | A | G | 19 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0174 others(16): Show |
19 | HG00735.hp1 HG01081.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1367+1311A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757866 | |||||||
| chrX:129757867 | G | A | 12 | a0001c0001t0001g0094 a0001c0001t0001g0119 a0001c0001t0001g0120 others(9): Show |
12 | HG00673.hp1 HG01346.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1367+1312G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757867 | |||||||
| chrX:129757868 | A | G | 12 | a0001c0001t0001g0066 a0001c0001t0001g0173 a0001c0001t0002g0024 others(9): Show |
12 | HG01167.hp1 HG01169.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1368-1312A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757868 | |||||||
| chrX:129757869 | G | A | 68 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0121 others(65): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1368-1311G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757869 | |||||||
| chrX:129757870 | A | G | 25 | a0001c0001t0001g0001 a0001c0001t0001g0125 a0001c0001t0001g0153 others(22): Show |
26 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1368-1310A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757870 | |||||||
| chrX:129757871 | G | A | 2 | a0001c0001t0001g0094 a0001c0002t0001g0072 |
2 | NA18939.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1368-1309G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757871 | |||||||
| chrX:129757872 | A | G | 9 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0131 others(6): Show |
9 | HG00673.hp1 HG01346.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1368-1308A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757872 | |||||||
| chrX:129757873 | A | AAGAAAGA others(13): Show |
1 | a0001c0002t0001g0259 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1368-1304_1368-130 others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | ||||||
| chrX:129757873 | A | AAGAAAGA others(7): Show |
1 | a0001c0001t0002g0036 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1368-1304_1368-130 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | ||||||
| chrX:129757873 | A | AAGAAAGA others(3): Show |
1 | a0001c0001t0001g0121 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1368-1304_1368-130 others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | ||||||
| chrX:129757873 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0094 others(89): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1368-1307A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757873 | |||||||
| chrX:129757873 | AAG | A | 13 | a0001c0001t0001g0075 a0001c0001t0001g0181 a0001c0001t0001g0277 others(10): Show |
13 | HG01496.hp2 HG01934.hp1 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.1368-1285_1368-128 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757873 | ||||||
| chrX:129757874 | A | AGAGG | 4 | a0001c0001t0003g0092 a0001c0001t0003g0167 a0001c0002t0001g0251 others(1): Show |
4 | HG00621.hp1 HG01258.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368-1303_1368-130 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757874 | ||||||
| chrX:129757874 | A | G | 17 | a0001c0001t0003g0085 a0001c0001t0003g0086 a0001c0001t0003g0104 others(14): Show |
18 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(15): Show |
intron_variant | MODIFIER | c.1368-1306A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757874 | |||||||
| chrX:129757876 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0141 a0001c0002t0001g0072 |
3 | NA18939.hp2 NA18960.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1368-1304A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757876 | |||||||
| chrX:129757877 | G | A | 26 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0174 others(23): Show |
26 | HG00597.hp2 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1368-1303G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757877 | |||||||
| chrX:129757877 | G | GGGAGAGA others(5): Show |
2 | a0001c0001t0003g0080 a0001c0002t0001g0280 |
2 | NA18948.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1368-1303_1368-130 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757877 | |||||||
| chrX:129757878 | A | G | 29 | a0001c0001t0001g0097 a0001c0001t0001g0123 a0001c0001t0002g0068 others(26): Show |
29 | HG00099.hp2 HG00597.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1368-1302A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757878 | |||||||
| chrX:129757879 | G | A | 12 | a0001c0001t0001g0066 a0001c0001t0001g0173 a0001c0001t0002g0024 others(9): Show |
12 | HG01167.hp1 HG01169.hp1 HG02056.hp1 others(9): Show |
intron_variant | MODIFIER | c.1368-1301G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757879 | |||||||
| chrX:129757880 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1368-1300A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757880 | |||||||
| chrX:129757881 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0125 a0001c0001t0001g0153 others(29): Show |
33 | HG00597.hp2 HG00741.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1368-1299G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757881 | |||||||
| chrX:129757882 | A | G | 6 | a0001c0001t0003g0298 a0001c0001t0018g0209 a0001c0002t0001g0073 others(3): Show |
6 | HG01175.hp2 HG01255.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1368-1298A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757882 | |||||||
| chrX:129757883 | G | A | 12 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(9): Show |
12 | HG00673.hp1 HG01346.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1368-1297G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757883 | |||||||
| chrX:129757883 | GAGAGAGA others(7): Show |
G | 1 | a0001c0001t0007g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1368-1293_1368-128 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757883 | ||||||
| chrX:129757883 | GAGAGAGA others(11): Show |
G | 3 | a0001c0001t0005g0013 a0001c0001t0005g0160 a0001c0001t0007g0286 |
3 | HG02615.hp2 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1368-1293_1368-127 others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757883 | ||||||
| chrX:129757883 | GAGAGAGA others(15): Show |
G | 2 | a0001c0001t0005g0012 a0001c0001t0007g0285 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1368-1293_1368-127 others(26): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757883 | ||||||
| chrX:129757883 | GAGAGAGA others(19): Show |
G | 1 | a0001c0001t0005g0011 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1368-1293_1368-126 others(30): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757883 | ||||||
| chrX:129757885 | G | A | 23 | a0001c0001t0003g0085 a0001c0001t0003g0086 a0001c0001t0003g0092 others(20): Show |
24 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.1368-1295G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757885 | |||||||
| chrX:129757885 | GAGAGAGA others(13): Show |
G | 1 | a0001c0001t0005g0002 | 2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1368-1291_1368-127 others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757885 | ||||||
| chrX:129757885 | GAGAGAGA others(17): Show |
G | 5 | a0001c0001t0005g0192 a0001c0001t0005g0193 a0001c0001t0005g0208 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1368-1291_1368-126 others(28): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757885 | ||||||
| chrX:129757886 | A | G | 3 | a0001c0001t0002g0022 a0001c0001t0003g0060 a0001c0002t0001g0087 |
3 | HG00597.hp2 NA18949.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1368-1294A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757886 | |||||||
| chrX:129757887 | G | A | 7 | a0001c0001t0001g0094 a0001c0001t0001g0122 a0001c0001t0001g0140 others(4): Show |
7 | NA18939.hp2 NA18957.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-1293G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757887 | |||||||
| chrX:129757887 | GAGAGAGA others(7): Show |
G | 1 | a0001c0001t0002g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1368-1289_1368-127 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757887 | ||||||
| chrX:129757887 | GAGAGAGA others(11): Show |
G | 7 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(4): Show |
7 | HG01496.hp1 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-1289_1368-127 others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757887 | ||||||
| chrX:129757887 | GAGAGAGA others(15): Show |
G | 1 | a0001c0001t0002g0065 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1368-1289_1368-126 others(26): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757887 | ||||||
| chrX:129757889 | G | A | 26 | a0001c0001t0001g0097 a0001c0001t0002g0068 a0001c0001t0002g0148 others(23): Show |
26 | HG00099.hp2 HG00597.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.1368-1291G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757889 | |||||||
| chrX:129757889 | G | GAGAAGAA others(4): Show |
1 | a0001c0001t0004g0037 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1368-1288_1368-128 others(15): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757889 | ||||||
| chrX:129757889 | GAGAGAGA others(5): Show |
G | 1 | a0001c0002t0001g0293 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1368-1287_1368-127 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757889 | ||||||
| chrX:129757889 | GAGAGAGA others(9): Show |
G | 3 | a0001c0001t0003g0116 a0001c0001t0006g0281 a0001c0001t0010g0134 |
3 | NA19030.hp1 NA19056.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1368-1287_1368-127 others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757889 | ||||||
| chrX:129757889 | GAGAGAGA others(13): Show |
G | 1 | a0001c0001t0006g0130 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1368-1287_1368-126 others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757889 | ||||||
| chrX:129757891 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1368-1289G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757891 | |||||||
| chrX:129757891 | GAGAGAA | G | 7 | a0001c0001t0001g0129 a0001c0001t0001g0169 a0001c0001t0002g0078 others(4): Show |
7 | HG00639.hp1 HG02015.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1368-1285_1368-128 others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | ||||||
| chrX:129757891 | GAGAGAAA others(3): Show |
G | 17 | a0001c0001t0001g0124 a0001c0001t0001g0128 a0001c0001t0002g0070 others(14): Show |
17 | HG00408.hp2 HG00544.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1368-1285_1368-127 others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | ||||||
| chrX:129757891 | GAGAGAAA others(7): Show |
G | 8 | a0001c0001t0001g0253 a0001c0001t0002g0018 a0001c0001t0002g0053 others(5): Show |
8 | HG03130.hp1 HG03239.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-1285_1368-127 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | ||||||
| chrX:129757891 | GAGAGAAA others(11): Show |
G | 6 | a0001c0001t0001g0151 a0001c0001t0001g0276 a0001c0001t0002g0138 others(3): Show |
6 | HG03098.hp1 HG03927.hp2 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.1368-1285_1368-126 others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | ||||||
| chrX:129757891 | GAGAGAAA others(15): Show |
G | 1 | a0001c0001t0002g0100 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1368-1285_1368-126 others(26): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | ||||||
| chrX:129757891 | GAGAGAAA others(19): Show |
G | 1 | a0001c0001t0001g0240 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1368-1285_1368-126 others(30): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757891 | ||||||
| chrX:129757893 | G | A | 12 | a0001c0001t0002g0067 a0001c0001t0002g0091 a0001c0001t0002g0175 others(9): Show |
12 | HG01175.hp2 HG01255.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1368-1287G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757893 | |||||||
| chrX:129757893 | GAGAA | G | 17 | a0001c0001t0001g0184 a0001c0001t0003g0027 a0001c0001t0003g0050 others(14): Show |
17 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.1368-1221_1368-121 others(8): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | ||||||
| chrX:129757893 | GAGAAAGA others(1): Show |
G | 11 | a0001c0001t0003g0023 a0001c0001t0003g0108 a0001c0001t0003g0158 others(8): Show |
11 | HG01071.hp2 HG01884.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1368-1225_1368-121 others(12): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | ||||||
| chrX:129757893 | GAGAAAGA others(4): Show |
G | 1 | a0001c0001t0012g0177 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1368-1285_1368-127 others(15): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | ||||||
| chrX:129757893 | GAGAAAGA others(5): Show |
G | 19 | a0001c0001t0002g0146 a0001c0001t0003g0016 a0001c0001t0003g0043 others(16): Show |
19 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1368-1229_1368-121 others(16): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | ||||||
| chrX:129757893 | GAGAAAGA others(9): Show |
G | 7 | a0001c0001t0003g0010 a0001c0002t0001g0004 a0001c0002t0001g0064 others(4): Show |
7 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(4): Show |
intron_variant | MODIFIER | c.1368-1233_1368-121 others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | ||||||
| chrX:129757893 | GAGAAAGA others(13): Show |
G | 2 | a0001c0001t0001g0093 a0001c0002t0001g0161 |
2 | HG03710.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1368-1237_1368-121 others(24): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757893 | ||||||
| chrX:129757895 | GAA | G | 10 | a0001c0001t0002g0117 a0001c0001t0002g0148 a0001c0001t0008g0201 others(7): Show |
10 | HG00597.hp1 HG02135.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.1368-1283_1368-128 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | ||||||
| chrX:129757895 | GAAAGAA | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0097 a0001c0001t0001g0166 others(11): Show |
15 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1368-1283_1368-127 others(10): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | ||||||
| chrX:129757895 | GAAAGAAA others(3): Show |
G | 10 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0127 others(7): Show |
10 | HG01175.hp1 HG01891.hp2 HG03654.hp1 others(7): Show |
intron_variant | MODIFIER | c.1368-1283_1368-127 others(14): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | ||||||
| chrX:129757895 | GAAAGAAA others(7): Show |
G | 4 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0003g0059 others(1): Show |
4 | HG01081.hp1 HG02723.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368-1283_1368-127 others(18): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | ||||||
| chrX:129757895 | GAAAGAAA others(11): Show |
G | 2 | a0001c0001t0002g0051 a0001c0002t0001g0272 |
2 | HG03041.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1368-1283_1368-126 others(22): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chrX | 129757895 | ||||||
| chrX:129757897 | A | G | 100 | a0001c0001t0001g0066 a0001c0001t0001g0094 a0001c0001t0001g0118 others(97): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.1368-1283A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757897 | |||||||
| chrX:129757901 | A | G | 83 | a0001c0001t0001g0094 a0001c0001t0001g0118 a0001c0001t0001g0119 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1368-1279A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757901 | |||||||
| chrX:129757905 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0094 a0001c0001t0001g0097 others(72): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.1368-1275A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757905 | |||||||
| chrX:129757907 | G | A | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1368-1273G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757907 | |||||||
| chrX:129757908 | A | G | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1368-1272A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757908 | |||||||
| chrX:129757909 | A | G | 32 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0123 others(29): Show |
32 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1368-1271A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757909 | |||||||
| chrX:129757913 | A | G | 8 | a0001c0001t0001g0097 a0001c0001t0002g0022 a0001c0001t0003g0060 others(5): Show |
8 | HG00597.hp2 HG01175.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.1368-1267A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757913 | |||||||
| chrX:129757917 | A | G | 3 | a0001c0001t0003g0060 a0001c0002t0001g0087 a0001c0002t0001g0272 |
3 | HG00597.hp2 HG03490.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1368-1263A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757917 | |||||||
| chrX:129757921 | A | G | 1 | a0001c0001t0003g0060 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1368-1259A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129757921 | |||||||
| chrX:129758000 | T | C | 41 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(38): Show |
41 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.1368-1180T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758000 | |||||||
| chrX:129758088 | T | G | 1 | a0001c0002t0001g0019 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1368-1092T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758088 | |||||||
| chrX:129758089 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1368-1091G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758089 | |||||||
| chrX:129758106 | G | A | 5 | a0001c0001t0004g0034 a0001c0001t0004g0037 a0001c0001t0004g0074 others(2): Show |
5 | HG01891.hp2 HG02155.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1368-1074G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758106 | |||||||
| chrX:129758165 | A | G | 1 | a0001c0001t0015g0223 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1368-1015A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758165 | |||||||
| chrX:129758446 | C | T | 41 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(38): Show |
41 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(38): Show |
intron_variant | MODIFIER | c.1368-734C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758446 | |||||||
| chrX:129758736 | G | A | 1 | a0001c0001t0002g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1368-444G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758736 | |||||||
| chrX:129758817 | T | A | 1 | a0001c0001t0003g0048 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1368-363T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129758817 | |||||||
| chrX:129759068 | C | T | 1 | a0001c0001t0006g0281 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1368-112C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 14/20 | chrX | 129759068 | |||||||
| chrX:129759273 | T | C | 36 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(33): Show |
36 | HG00673.hp1 HG01346.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.1428+33T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759273 | |||||||
| chrX:129759423 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1428+183C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759423 | |||||||
| chrX:129759441 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(69): Show |
74 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1428+201C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759441 | |||||||
| chrX:129759578 | C | T | 1 | a0001c0001t0003g0090 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1428+338C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759578 | |||||||
| chrX:129759582 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1428+342G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759582 | |||||||
| chrX:129759616 | T | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(128): Show |
133 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(130): Show |
intron_variant | MODIFIER | c.1428+376T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759616 | |||||||
| chrX:129759833 | A | C | 37 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(34): Show |
37 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.1428+593A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759833 | |||||||
| chrX:129759942 | G | A | 3 | a0001c0001t0006g0130 a0003c0004t0006g0096 a0003c0004t0006g0135 |
3 | NA18975.hp1 NA19065.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.1429-570G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129759942 | |||||||
| chrX:129759995 | TCAGCAGC others(11): Show |
T | 2 | a0001c0002t0001g0109 a0001c0002t0001g0225 |
2 | NA18969.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1429-513_1429-496d others(20): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chrX | 129759995 | ||||||
| chrX:129760013 | A | G | 4 | a0001c0001t0002g0022 a0001c0001t0002g0051 a0001c0001t0002g0068 others(1): Show |
4 | HG03041.hp1 HG03486.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1429-499A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760013 | |||||||
| chrX:129760042 | A | G | 7 | a0001c0001t0005g0002 a0001c0001t0005g0192 a0001c0001t0005g0193 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429-470A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760042 | |||||||
| chrX:129760048 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1429-464C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760048 | |||||||
| chrX:129760237 | C | T | 7 | a0001c0001t0005g0002 a0001c0001t0005g0192 a0001c0001t0005g0193 others(4): Show |
8 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429-275C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760237 | |||||||
| chrX:129760300 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1429-212G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760300 | |||||||
| chrX:129760430 | C | T | 1 | a0001c0006t0001g0143 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1429-82C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760430 | |||||||
| chrX:129760479 | G | A | 8 | a0001c0001t0002g0055 a0001c0001t0008g0201 a0001c0001t0008g0202 others(5): Show |
8 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429-33G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 15/20 | chrX | 129760479 | |||||||
| chrX:129760583 | T | A | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | splice_donor_variant&intron_variant | HIGH | c.1498+2T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760583 | |||||||
| chrX:129760592 | G | C | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+11G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760592 | |||||||
| chrX:129760594 | A | G | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+13A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760594 | |||||||
| chrX:129760719 | G | T | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+138G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760719 | |||||||
| chrX:129760756 | A | T | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1498+175A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760756 | |||||||
| chrX:129760917 | G | C | 3 | a0001c0001t0002g0020 a0001c0001t0002g0067 a0001c0001t0002g0278 |
3 | HG00544.hp2 HG00673.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1499-255G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760917 | |||||||
| chrX:129760949 | T | A | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-223T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129760949 | |||||||
| chrX:129761004 | C | A | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1499-168C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129761004 | |||||||
| chrX:129761014 | C | T | 37 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(34): Show |
37 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.1499-158C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 16/20 | chrX | 129761014 | |||||||
| chrX:129761308 | C | A | 1 | a0001c0002t0001g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1603+32C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761308 | |||||||
| chrX:129761311 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1603+35C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761311 | |||||||
| chrX:129761329 | A | G | 2 | a0001c0001t0002g0300 a0001c0001t0002g0301 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1603+53A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761329 | |||||||
| chrX:129761340 | G | A | 2 | a0002c0003t0002g0289 a0002c0003t0002g0292 |
2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1603+64G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761340 | |||||||
| chrX:129761387 | T | C | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+111T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761387 | |||||||
| chrX:129761388 | C | T | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+112C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761388 | |||||||
| chrX:129761389 | T | A | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+113T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761389 | |||||||
| chrX:129761538 | C | T | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+262C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761538 | |||||||
| chrX:129761579 | T | G | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+303T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761579 | |||||||
| chrX:129761580 | G | C | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+304G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761580 | |||||||
| chrX:129761597 | G | T | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1603+321G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761597 | |||||||
| chrX:129761741 | A | C | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-265A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761741 | |||||||
| chrX:129761742 | G | A | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-264G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761742 | |||||||
| chrX:129761748 | C | T | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-258C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761748 | |||||||
| chrX:129761749 | A | C | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-257A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761749 | |||||||
| chrX:129761751 | G | A | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-255G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761751 | |||||||
| chrX:129761772 | C | T | 1 | a0002c0003t0005g0217 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1604-234C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761772 | |||||||
| chrX:129761842 | A | C | 37 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(34): Show |
37 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.1604-164A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761842 | |||||||
| chrX:129761913 | G | T | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1604-93G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761913 | |||||||
| chrX:129761995 | T | G | 5 | a0001c0001t0005g0011 a0001c0001t0005g0012 a0001c0001t0005g0013 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1604-11T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 17/20 | chrX | 129761995 | |||||||
| chrX:129762070 | G | C | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.1663+5G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762070 | |||||||
| chrX:129762072 | C | G | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | splice_region_variant&intron_variant | LOW | c.1663+7C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762072 | |||||||
| chrX:129762181 | G | A | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0166 others(2): Show |
5 | NA18951.hp2 NA19059.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663+116G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762181 | |||||||
| chrX:129762314 | C | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0185 |
2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1663+249C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762314 | |||||||
| chrX:129762372 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(68): Show |
73 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.1663+307G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762372 | |||||||
| chrX:129762382 | G | A | 3 | a0001c0001t0002g0117 a0001c0001t0002g0197 a0001c0001t0002g0215 |
3 | HG01109.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1664-312G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762382 | |||||||
| chrX:129762461 | C | T | 1 | a0001c0001t0002g0018 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1664-233C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762461 | |||||||
| chrX:129762540 | C | T | 1 | a0002c0003t0005g0217 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1664-154C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762540 | |||||||
| chrX:129762555 | C | T | 3 | a0001c0001t0002g0100 a0001c0001t0002g0186 a0001c0001t0009g0204 |
3 | HG01891.hp2 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1664-139C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 18/20 | chrX | 129762555 | |||||||
| chrX:129763064 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(68): Show |
73 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.1740+294C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763064 | |||||||
| chrX:129763107 | G | C | 3 | a0001c0001t0002g0053 a0001c0001t0002g0136 a0001c0001t0002g0180 |
3 | HG02735.hp1 HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1740+337G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763107 | |||||||
| chrX:129763268 | A | G | 2 | a0002c0003t0002g0289 a0002c0003t0002g0292 |
2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1740+498A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763268 | |||||||
| chrX:129763281 | C | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(68): Show |
73 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.1740+511C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763281 | |||||||
| chrX:129763475 | C | T | 1 | a0001c0002t0001g0248 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1740+705C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763475 | |||||||
| chrX:129763523 | T | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(67): Show |
72 | HG00408.hp2 HG00639.hp1 HG01069.hp1 others(69): Show |
intron_variant | MODIFIER | c.1740+753T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763523 | |||||||
| chrX:129763532 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1740+762C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763532 | |||||||
| chrX:129763564 | C | T | 2 | a0002c0003t0002g0289 a0002c0003t0002g0292 |
2 | HG01243.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1740+794C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763564 | |||||||
| chrX:129763854 | T | G | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1084T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763854 | |||||||
| chrX:129763963 | G | C | 2 | a0001c0001t0002g0194 a0001c0001t0002g0200 |
2 | HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1740+1193G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129763963 | |||||||
| chrX:129764124 | T | G | 1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+1354T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764124 | |||||||
| chrX:129764245 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(128): Show |
133 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(130): Show |
intron_variant | MODIFIER | c.1740+1475G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764245 | |||||||
| chrX:129764265 | A | G | 2 | a0001c0001t0004g0039 a0001c0001t0004g0045 |
2 | NA18970.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.1740+1495A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764265 | |||||||
| chrX:129764301 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1740+1531T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764301 | |||||||
| chrX:129764511 | C | T | 3 | a0002c0003t0002g0289 a0002c0003t0002g0292 a0002c0003t0005g0217 |
3 | HG01243.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1740+1741C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764511 | |||||||
| chrX:129764517 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(197): Show |
202 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.1740+1747T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764517 | |||||||
| chrX:129764572 | T | A | 3 | a0002c0003t0002g0289 a0002c0003t0002g0292 a0002c0003t0005g0217 |
3 | HG01243.hp1 HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1740+1802T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764572 | |||||||
| chrX:129764586 | C | T | 1 | a0001c0002t0001g0219 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1740+1816C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764586 | |||||||
| chrX:129764655 | C | CA | 13 | a0001c0001t0003g0025 a0001c0001t0003g0132 a0001c0001t0005g0011 others(10): Show |
13 | HG00099.hp2 HG01243.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1740+1901dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764655 | ||||||
| chrX:129764655 | CA | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(110): Show |
115 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(112): Show |
intron_variant | MODIFIER | c.1740+1901delA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129764655 | ||||||
| chrX:129764951 | G | A | 2 | a0001c0001t0001g0093 a0005c0011t0001g0252 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1740+2181G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764951 | |||||||
| chrX:129764977 | A | C | 17 | a0001c0001t0002g0055 a0001c0001t0003g0059 a0001c0001t0003g0114 others(14): Show |
17 | HG01081.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1740+2207A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129764977 | |||||||
| chrX:129765012 | T | TCTTTCTT others(10): Show |
1 | a0008c0008t0003g0009 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1740+2246_1740+226 others(21): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765012 | ||||||
| chrX:129765060 | G | A | 1 | a0001c0001t0004g0026 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1740+2290G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765060 | |||||||
| chrX:129765178 | G | T | 7 | a0001c0001t0003g0059 a0001c0001t0003g0114 a0001c0001t0003g0115 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1740+2408G>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765178 | |||||||
| chrX:129765371 | C | A | 7 | a0001c0001t0003g0059 a0001c0001t0003g0114 a0001c0001t0003g0115 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1741-2232C>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765371 | |||||||
| chrX:129765503 | G | C | 1 | a0001c0001t0005g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1741-2100G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765503 | |||||||
| chrX:129765554 | A | C | 1 | a0001c0001t0002g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1741-2049A>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765554 | |||||||
| chrX:129765619 | T | C | 3 | a0001c0001t0002g0117 a0001c0001t0002g0197 a0001c0001t0002g0215 |
3 | HG01109.hp1 HG02886.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1741-1984T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765619 | |||||||
| chrX:129765635 | C | CT | 26 | a0001c0001t0002g0117 a0001c0001t0002g0301 a0001c0001t0005g0002 others(23): Show |
27 | HG00323.hp1 HG01123.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.1741-1946dupT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765635 | ||||||
| chrX:129765635 | C | CTT | 15 | a0001c0001t0003g0059 a0001c0001t0003g0114 a0001c0001t0003g0115 others(12): Show |
15 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1741-1947_1741-194 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765635 | ||||||
| chrX:129765635 | CT | C | 66 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0128 others(63): Show |
66 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1741-1946delT | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765635 | ||||||
| chrX:129765635 | CTT | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(58): Show |
63 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1741-1947_1741-194 others(6): Show |
XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129765635 | ||||||
| chrX:129765649 | T | C | 1 | a0001c0002t0016g0246 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1741-1954T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765649 | |||||||
| chrX:129765651 | T | A | 25 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(22): Show |
25 | HG00544.hp2 HG00673.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1741-1952T>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765651 | |||||||
| chrX:129765714 | T | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(210): Show |
216 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1741-1889T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765714 | |||||||
| chrX:129765783 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0075 others(159): Show |
164 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.1741-1820A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129765783 | |||||||
| chrX:129766011 | T | C | 1 | a0001c0001t0005g0015 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1741-1592T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129766011 | |||||||
| chrX:129766324 | C | T | 1 | a0001c0001t0003g0052 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1741-1279C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129766324 | |||||||
| chrX:129766396 | G | A | 1 | a0001c0002t0001g0064 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1741-1207G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129766396 | |||||||
| chrX:129766583 | G | A | 4 | a0001c0001t0002g0194 a0001c0001t0002g0200 a0001c0001t0011g0008 others(1): Show |
5 | HG02109.hp1 HG06807.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1741-1020G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129766583 | |||||||
| chrX:129766865 | C | T | 18 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0005g0002 others(15): Show |
19 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1741-738C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129766865 | |||||||
| chrX:129767041 | T | G | 14 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0007g0007 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1741-562T>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767041 | |||||||
| chrX:129767213 | C | CA | 14 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0007g0007 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1741-382dupA | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chrX | 129767213 | ||||||
| chrX:129767234 | A | T | 8 | a0001c0001t0007g0007 a0001c0001t0007g0284 a0001c0001t0007g0285 others(5): Show |
8 | HG02258.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1741-369A>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767234 | |||||||
| chrX:129767264 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1741-339A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767264 | |||||||
| chrX:129767265 | A | G | 1 | a0001c0002t0001g0272 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1741-338A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767265 | |||||||
| chrX:129767281 | T | C | 6 | a0001c0001t0008g0201 a0001c0001t0008g0202 a0001c0001t0008g0211 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1741-322T>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767281 | |||||||
| chrX:129767455 | A | G | 14 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0007g0007 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1741-148A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767455 | |||||||
| chrX:129767495 | G | C | 1 | a0001c0002t0001g0263 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1741-108G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767495 | |||||||
| chrX:129767515 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1741-88C>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767515 | |||||||
| chrX:129767516 | G | C | 1 | a0001c0001t0002g0216 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1741-87G>C | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 19/20 | chrX | 129767516 | |||||||
| chrX:129767976 | C | T | 1 | a0001c0010t0005g0213 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1830+284C>T | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | chrX | 129767976 | |||||||
| chrX:129768051 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1831-240G>A | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | chrX | 129768051 | |||||||
| chrX:129768259 | A | G | 14 | a0001c0001t0002g0300 a0001c0001t0002g0301 a0001c0001t0007g0007 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1831-32A>G | XPNPEP2 | ENSG00000122121.12 | transcript | ENST00000371106.4 | protein_coding | 20/20 | chrX | 129768259 |