Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57089 |
| ensemblid | ENSG00000198018.7 |
| hgncid | 19745 |
| symbol | ENTPD7 |
| name | ectonucleoside triphosphate diphosphohydrolase 7 |
| refseq_nuc | NM_020354.5 |
| refseq_prot | NP_065087.1 |
| ensembl_nuc | ENST00000370489.5 |
| ensembl_prot | ENSP00000359520.4 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 99659509 |
| end | 99711241 |
| strand | + |
| ver | v1.2 |
| region | chr10:99659509-99711241 |
| region5000 | chr10:99654509-99716241 |
| regionname0 | ENTPD7_chr10_99659509_99711241 |
| regionname5000 | ENTPD7_chr10_99654509_99716241 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 604 | 305 | 63 | 63 | 133 | 12 | 32 | 107 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | MARIS others(599): Show |
chr10 | 99654509 | 99716241 |
| a0002 | 0/0 | 604 | 96 | 16 | 16 | 50 | 4 | 10 | 42 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | MARIS others(599): Show |
chr10 | 99654509 | 99716241 |
| a0003 | 0/0 | 604 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | MARIS others(599): Show |
chr10 | 99654509 | 99716241 |
| a0004 | 0/0 | 604 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | MARIS others(599): Show |
chr10 | 99654509 | 99716241 |
| a0005 | 0/0 | 604 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | MARIS others(599): Show |
chr10 | 99654509 | 99716241 |
| a0006 | 0/0 | 604 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | MARIS others(599): Show |
chr10 | 99654509 | 99716241 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1812 | 294 | 54 | 63 | 132 | 12 | 31 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0001c0003 | 0/0 | 1812 | 5 | 5 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0001c0005 | 0/0 | 1812 | 3 | 3 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0001c0009 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0001c0011 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0001c0013 | 0/0 | 1812 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0002c0002 | 0/0 | 1812 | 94 | 16 | 16 | 48 | 4 | 10 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0002c0006 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0002c0008 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0003c0004 | 0/0 | 1812 | 4 | 4 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0004c0010 | 0/0 | 1812 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0005c0007 | 0/0 | 1812 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 | ||
| a0006c0012 | 0/0 | 1812 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | ATGGC others(1807): Show |
chr10 | 99654509 | 99716241 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8548 | 4 | 4 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0002 | 0/0 | 8548 | 69 | 5 | 7 | 50 | 1 | 6 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0003 | 0/0 | 8549 | 65 | 15 | 14 | 26 | 0 | 10 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0004 | 0/0 | 8548 | 54 | 0 | 8 | 37 | 5 | 4 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0005 | 0/0 | 8549 | 43 | 9 | 19 | 6 | 2 | 7 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0007 | 0/0 | 8549 | 10 | 0 | 3 | 7 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0009 | 1/0 | 8548 | 6 | 3 | 2 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0010 | 0/0 | 8548 | 4 | 1 | 3 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0011 | 0/0 | 8549 | 4 | 0 | 2 | 0 | 1 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0012 | 0/0 | 8548 | 4 | 4 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0014 | 0/0 | 8549 | 3 | 0 | 0 | 2 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0015 | 0/0 | 8548 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0016 | 0/0 | 8548 | 2 | 0 | 0 | 0 | 2 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0017 | 0/0 | 8548 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0018 | 0/0 | 8549 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0019 | 0/0 | 8548 | 2 | 0 | 1 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0020 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0021 | 0/0 | 8548 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0022 | 0/0 | 8549 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0023 | 0/1 | 8548 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0024 | 0/0 | 8549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0026 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0027 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0032 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0033 | 0/0 | 8549 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0035 | 0/0 | 8549 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0036 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0037 | 0/0 | 8549 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0038 | 0/0 | 8549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0039 | 0/0 | 8549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0040 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0041 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0042 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0001t0043 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0003t0001 | 0/0 | 8548 | 4 | 4 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0003t0029 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0005t0008 | 0/0 | 8548 | 3 | 3 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0009t0002 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0001c0011t0003 | 0/0 | 8549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0001c0013t0003 | 0/0 | 8549 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0002c0002t0001 | 0/0 | 8548 | 74 | 7 | 11 | 42 | 4 | 10 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0002c0002t0006 | 0/0 | 8548 | 12 | 9 | 3 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0002c0002t0013 | 0/0 | 8548 | 3 | 0 | 0 | 3 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0002c0002t0025 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0002c0002t0028 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0002c0002t0030 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0002c0002t0031 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0002c0002t0034 | 0/0 | 8548 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0002c0006t0001 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0002c0008t0003 | 0/0 | 8549 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0003c0004t0008 | 0/0 | 8548 | 4 | 4 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0004c0010t0005 | 0/0 | 8549 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8544): Show |
chr10 | 99654509 | 99716241 |
| a0005c0007t0001 | 0/0 | 8548 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| a0006c0012t0002 | 0/0 | 8548 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | CCGGC others(8543): Show |
chr10 | 99654509 | 99716241 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0014 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0010 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0007g0013 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0007g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0007g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0007g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0009g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0009g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0009g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0009g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0010g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0010g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0010g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0011g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0011g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0012g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0014g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0014g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0014g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0015g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0016g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0017g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0018g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0018g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0019g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0019g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0020g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0021g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0022g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0023g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0024g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0026g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0027g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0032g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0033g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0035g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0036g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0037g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0038g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0039g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0040g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0041g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0042g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0001t0043g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0003t0029g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0005t0008g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0009t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0011t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0001c0013t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0003 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0004 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0007 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0006g0002 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0013g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0013g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0013g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0025g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0028g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0030g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0031g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0002t0034g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0006t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0002c0008t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0003c0004t0008g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0003c0004t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0004c0010t0005g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0005c0007t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| a0006c0012t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0022 | EUR | GBR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00099 | hp2 | a0001 | c0001 | t0011 | g0217 | EUR | GBR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0016 | EUR | GBR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0014 | EUR | GBR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00280 | hp1 | a0001 | c0001 | t0022 | g0043 | EUR | FIN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0023 | EUR | FIN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00423 | hp2 | a0001 | c0001 | t0007 | g0013 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00558 | hp1 | a0002 | c0002 | t0031 | g0148 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0290 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00639 | hp1 | a0001 | c0001 | t0011 | g0017 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00639 | hp2 | a0001 | c0001 | t0010 | g0108 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00642 | hp2 | a0002 | c0002 | t0034 | g0004 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00673 | hp2 | a0002 | c0002 | t0030 | g0130 | EAS | CHS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0306 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00738 | hp1 | a0002 | c0002 | t0028 | g0128 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0276 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0091 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0074 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01074 | hp1 | a0001 | c0001 | t0011 | g0247 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01074 | hp2 | a0004 | c0010 | t0005 | g0286 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0303 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01099 | hp1 | a0001 | c0001 | t0026 | g0034 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0045 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01167 | hp2 | a0001 | c0001 | t0043 | g0080 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0288 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0266 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01192 | hp1 | a0001 | c0001 | t0009 | g0084 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01192 | hp2 | a0001 | c0001 | t0019 | g0239 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01243 | hp1 | a0002 | c0002 | t0006 | g0002 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01255 | hp2 | a0001 | c0001 | t0009 | g0082 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01257 | hp1 | a0001 | c0001 | t0010 | g0026 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0299 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01258 | hp2 | a0001 | c0001 | t0010 | g0026 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0282 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01358 | hp1 | a0002 | c0002 | t0006 | g0002 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0081 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01433 | hp1 | a0001 | c0001 | t0035 | g0296 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01433 | hp2 | a0001 | c0001 | t0036 | g0300 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0045 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01496 | hp2 | a0002 | c0002 | t0006 | g0109 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0052 | EUR | IBS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0021 | EUR | IBS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0307 | EUR | IBS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01516 | hp2 | a0001 | c0001 | t0016 | g0033 | EUR | IBS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0051 | EUR | IBS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01517 | hp2 | a0001 | c0001 | t0016 | g0033 | EUR | IBS | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0158 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0269 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0309 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0042 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0248 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01978 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01993 | hp1 | a0001 | c0001 | t0005 | g0268 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0273 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02004 | hp1 | a0001 | c0001 | t0007 | g0222 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0043 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0165 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0142 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0258 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | CDX | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02155 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | CDX | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | CDX | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CDX | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02257 | hp2 | a0002 | c0002 | t0006 | g0110 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02273 | hp2 | a0001 | c0001 | t0004 | g0075 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02293 | hp1 | a0001 | c0001 | t0007 | g0013 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0042 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02451 | hp1 | a0001 | c0001 | t0041 | g0095 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02451 | hp2 | a0001 | c0001 | t0010 | g0106 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02523 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02523 | hp2 | a0001 | c0001 | t0014 | g0285 | EAS | KHV | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02615 | hp1 | a0003 | c0004 | t0008 | g0005 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02615 | hp2 | a0001 | c0001 | t0032 | g0166 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02622 | hp1 | a0002 | c0002 | t0006 | g0116 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02622 | hp2 | a0001 | c0005 | t0008 | g0005 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02630 | hp1 | a0001 | c0001 | t0012 | g0015 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02630 | hp2 | a0001 | c0001 | t0015 | g0037 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02647 | hp1 | a0005 | c0007 | t0001 | g0105 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0156 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0053 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0260 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0289 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0301 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02717 | hp2 | a0001 | c0001 | t0015 | g0037 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02723 | hp1 | a0001 | c0001 | t0018 | g0262 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02735 | hp1 | a0001 | c0001 | t0011 | g0017 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0018 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0149 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02809 | hp2 | a0002 | c0002 | t0006 | g0002 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02895 | hp1 | a0001 | c0001 | t0017 | g0025 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02895 | hp2 | a0002 | c0002 | t0006 | g0002 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02896 | hp2 | a0001 | c0005 | t0008 | g0005 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02897 | hp2 | a0001 | c0001 | t0017 | g0025 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | ESN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0055 | AFR | ESN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | ESN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0283 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0277 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03098 | hp2 | a0002 | c0002 | t0006 | g0117 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0083 | AFR | ESN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03130 | hp2 | a0001 | c0011 | t0003 | g0244 | AFR | ESN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0160 | AFR | ESN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03139 | hp2 | a0001 | c0001 | t0012 | g0015 | AFR | ESN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03195 | hp1 | a0002 | c0002 | t0006 | g0111 | AFR | ESN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03195 | hp2 | a0001 | c0001 | t0012 | g0015 | AFR | ESN | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0311 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03225 | hp2 | a0002 | c0002 | t0006 | g0002 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03239 | hp1 | a0001 | c0001 | t0021 | g0206 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0102 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0096 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0298 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0234 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0302 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03540 | hp2 | a0003 | c0004 | t0008 | g0005 | AFR | GWD | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0304 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0157 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0275 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0140 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0308 | SAS | PJL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | STU | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0227 | SAS | STU | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | BEB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0236 | SAS | BEB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03834 | hp1 | a0001 | c0001 | t0014 | g0297 | SAS | BEB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0125 | SAS | BEB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0069 | SAS | BEB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0118 | SAS | BEB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0259 | SAS | STU | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG04115 | hp2 | a0001 | c0001 | t0037 | g0256 | SAS | STU | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0147 | SAS | BEB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0310 | SAS | BEB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0079 | SAS | STU | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG04199 | hp2 | a0001 | c0013 | t0003 | g0020 | SAS | STU | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | STU | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0218 | SAS | STU | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | STU | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0274 | SAS | STU | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0159 | AFR | YRI | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | YRI | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | YRI | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18906 | hp2 | a0001 | c0001 | t0042 | g0097 | AFR | YRI | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18941 | hp1 | a0002 | c0006 | t0001 | g0127 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0070 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18943 | hp1 | a0002 | c0002 | t0025 | g0115 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18945 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18959 | hp2 | a0001 | c0001 | t0019 | g0220 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18964 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18968 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18974 | hp2 | a0001 | c0001 | t0014 | g0295 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18979 | hp1 | a0001 | c0009 | t0002 | g0001 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18982 | hp2 | a0001 | c0001 | t0033 | g0270 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18984 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18989 | hp1 | a0006 | c0012 | t0002 | g0178 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18992 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18997 | hp1 | a0002 | c0008 | t0003 | g0257 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18998 | hp1 | a0001 | c0001 | t0020 | g0065 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0265 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19006 | hp2 | a0002 | c0002 | t0013 | g0144 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19030 | hp1 | a0001 | c0001 | t0039 | g0305 | AFR | LWK | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19030 | hp2 | a0003 | c0004 | t0008 | g0005 | AFR | LWK | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | LWK | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19043 | hp2 | a0001 | c0001 | t0024 | g0245 | AFR | LWK | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19055 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19056 | hp1 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19066 | hp1 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19075 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19076 | hp2 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19080 | hp2 | a0002 | c0002 | t0013 | g0132 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19084 | hp2 | a0001 | c0001 | t0007 | g0255 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19085 | hp1 | a0002 | c0002 | t0013 | g0137 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19089 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19091 | hp2 | a0001 | c0001 | t0027 | g0001 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19240 | hp1 | a0001 | c0001 | t0038 | g0293 | AFR | YRI | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA19240 | hp2 | a0002 | c0002 | t0006 | g0002 | AFR | YRI | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | ASW | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | ASW | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0134 | EUR | TSI | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0169 | EUR | TSI | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0100 | EUR | TSI | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0287 | EUR | TSI | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0225 | SAS | GIH | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0034 | SAS | GIH | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0170 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | CLM | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02109 | hp1 | a0001 | c0005 | t0008 | g0005 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02109 | hp2 | a0002 | c0002 | t0006 | g0002 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0155 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0101 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | ACB | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03471 | hp1 | a0003 | c0004 | t0008 | g0168 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG03471 | hp2 | a0001 | c0003 | t0029 | g0107 | AFR | MSL | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG06807 | hp1 | a0001 | c0001 | t0018 | g0261 | AFR | USA | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0103 | AFR | USA | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0291 | AFR | USA | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0292 | AFR | USA | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA21309 | hp1 | a0001 | c0001 | t0040 | g0167 | AFR | LWK | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | LWK | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0023 | g0162 | REF | REF | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0009 | g0056 | REF | REF | ENTPD7_chr10_99654509_99716241 | ENTPD7 | chr10 | 99654509 | 99716241 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:99661610 | G | A | 1 | a0005 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.173G>A | p.Arg58Gln | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/13 | 348/8548 | 173/1815 | 58/604 | chr10 | 99661610 | |||
| chr10:99691502 | T | C | 1 | a0002 | 96 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(93): Show |
missense_variant | MODERATE | c.827T>C | p.Val276Ala | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/13 | 1002/8548 | 827/1815 | 276/604 | chr10 | 99691502 | |||
| chr10:99698601 | C | T | 1 | a0003 | 4 | HG02615.hp1 HG03471.hp1 HG03540.hp2 others(1): Show |
missense_variant | MODERATE | c.1078C>T | p.Leu360Phe | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/13 | 1253/8548 | 1078/1815 | 360/604 | chr10 | 99698601 | |||
| chr10:99698853 | G | A | 1 | a0004 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.1330G>A | p.Ala444Thr | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/13 | 1505/8548 | 1330/1815 | 444/604 | chr10 | 99698853 | |||
| chr10:99704610 | G | A | 1 | a0006 | 1 | NA18989.hp1 | missense_variant | MODERATE | c.1742G>A | p.Arg581Gln | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1917/8548 | 1742/1815 | 581/604 | chr10 | 99704610 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:99661590 | T | C | 1 | a0002c0006 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.153T>C | p.His51His | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/13 | 328/8548 | 153/1815 | 51/604 | chr10 | 99661590 | |||
| chr10:99685834 | A | C | 4 | a0001c0003 a0002c0002 a0002c0006 others(1): Show |
101 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(98): Show |
synonymous_variant | LOW | c.591A>C | p.Pro197Pro | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/13 | 766/8548 | 591/1815 | 197/604 | chr10 | 99685834 | |||
| chr10:99691437 | A | C | 1 | a0001c0013 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.762A>C | p.Val254Val | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/13 | 937/8548 | 762/1815 | 254/604 | chr10 | 99691437 | |||
| chr10:99696057 | C | T | 2 | a0001c0005 a0003c0004 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
synonymous_variant | LOW | c.945C>T | p.Phe315Phe | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/13 | 1120/8548 | 945/1815 | 315/604 | chr10 | 99696057 | |||
| chr10:99698786 | T | C | 1 | a0001c0009 | 1 | NA18979.hp1 | synonymous_variant | LOW | c.1263T>C | p.Phe421Phe | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/13 | 1438/8548 | 1263/1815 | 421/604 | chr10 | 99698786 | |||
| chr10:99702632 | G | A | 1 | a0001c0011 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1542G>A | p.Thr514Thr | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/13 | 1717/8548 | 1542/1815 | 514/604 | chr10 | 99702632 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:99659546 | T | C | 1 | a0001c0001t0015 | 2 | HG02630.hp2 HG02717.hp2 |
5_prime_UTR_variant | MODIFIER | c.-138T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 1/13 | 411 | chr10 | 99659546 | ||||||
| chr10:99659556 | G | A | 1 | a0001c0001t0020 | 1 | NA18998.hp1 | 5_prime_UTR_variant | MODIFIER | c.-128G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 1/13 | 401 | chr10 | 99659556 | ||||||
| chr10:99659569 | C | A | 2 | a0001c0005t0008 a0003c0004t0008 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-115C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 1/13 | 388 | chr10 | 99659569 | ||||||
| chr10:99704726 | T | C | 1 | a0001c0001t0016 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*43T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 43 | chr10 | 99704726 | ||||||
| chr10:99704800 | G | A | 1 | a0001c0001t0021 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*117G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 117 | chr10 | 99704800 | ||||||
| chr10:99705128 | T | C | 1 | a0001c0001t0022 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*445T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 445 | chr10 | 99705128 | ||||||
| chr10:99705183 | A | G | 1 | a0001c0001t0043 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*500A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 500 | chr10 | 99705183 | ||||||
| chr10:99705186 | G | A | 1 | a0001c0001t0024 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*503G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 503 | chr10 | 99705186 | ||||||
| chr10:99705718 | T | C | 1 | a0002c0002t0025 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1035T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1035 | chr10 | 99705718 | ||||||
| chr10:99705951 | T | C | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0010 others(22): Show |
192 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*1268T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1268 | chr10 | 99705951 | ||||||
| chr10:99706023 | G | A | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*1340G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1340 | chr10 | 99706023 | ||||||
| chr10:99706067 | C | G | 1 | a0001c0001t0015 | 2 | HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1384C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1384 | chr10 | 99706067 | ||||||
| chr10:99706123 | C | T | 1 | a0002c0002t0034 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1440C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1440 | chr10 | 99706123 | ||||||
| chr10:99706336 | C | CT | 19 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(16): Show |
141 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1664dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1665 | INFO_REALIGN_3_PRIME | chr10 | 99706336 | |||||
| chr10:99706366 | C | T | 1 | a0001c0001t0039 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1683C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1683 | chr10 | 99706366 | ||||||
| chr10:99706395 | G | A | 1 | a0002c0002t0013 | 3 | NA19006.hp2 NA19080.hp2 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1712G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1712 | chr10 | 99706395 | ||||||
| chr10:99706413 | G | A | 1 | a0001c0001t0040 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1730G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1730 | chr10 | 99706413 | ||||||
| chr10:99706513 | TA | T | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*1831delA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1831 | chr10 | 99706513 | ||||||
| chr10:99706548 | T | C | 8 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0016 others(5): Show |
80 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1865T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 1865 | chr10 | 99706548 | ||||||
| chr10:99706741 | C | T | 1 | a0001c0001t0038 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2058C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 2058 | chr10 | 99706741 | ||||||
| chr10:99706806 | C | T | 1 | a0001c0001t0015 | 2 | HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2123C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 2123 | chr10 | 99706806 | ||||||
| chr10:99706849 | G | T | 19 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(16): Show |
141 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2166G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 2166 | chr10 | 99706849 | ||||||
| chr10:99706863 | C | T | 19 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(16): Show |
141 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2180C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 2180 | chr10 | 99706863 | ||||||
| chr10:99707097 | T | C | 1 | a0001c0001t0015 | 2 | HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2414T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 2414 | chr10 | 99707097 | ||||||
| chr10:99707172 | G | A | 1 | a0001c0001t0033 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2489G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 2489 | chr10 | 99707172 | ||||||
| chr10:99707226 | C | G | 10 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0011 others(7): Show |
88 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*2543C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 2543 | chr10 | 99707226 | ||||||
| chr10:99707420 | C | T | 2 | a0001c0001t0017 a0001c0001t0032 |
3 | HG02615.hp2 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2737C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 2737 | chr10 | 99707420 | ||||||
| chr10:99707914 | A | G | 1 | a0001c0001t0037 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3231A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 3231 | chr10 | 99707914 | ||||||
| chr10:99708217 | T | G | 1 | a0001c0001t0026 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3534T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 3534 | chr10 | 99708217 | ||||||
| chr10:99708318 | C | A | 1 | a0001c0001t0018 | 2 | HG02723.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3635C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 3635 | chr10 | 99708318 | ||||||
| chr10:99708590 | T | G | 1 | a0001c0001t0041 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3907T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 3907 | chr10 | 99708590 | ||||||
| chr10:99708674 | G | A | 1 | a0002c0002t0028 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3991G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 3991 | chr10 | 99708674 | ||||||
| chr10:99708941 | A | G | 2 | a0001c0001t0012 a0001c0001t0042 |
5 | HG02630.hp1 HG03139.hp2 HG03195.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4258A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 4258 | chr10 | 99708941 | ||||||
| chr10:99708979 | T | C | 1 | a0001c0001t0040 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4296T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 4296 | chr10 | 99708979 | ||||||
| chr10:99708981 | T | C | 1 | a0001c0001t0032 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4298T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 4298 | chr10 | 99708981 | ||||||
| chr10:99709196 | G | A | 2 | a0001c0005t0008 a0003c0004t0008 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4513G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 4513 | chr10 | 99709196 | ||||||
| chr10:99709304 | A | C | 1 | a0001c0001t0040 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4621A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 4621 | chr10 | 99709304 | ||||||
| chr10:99709371 | G | A | 1 | a0001c0001t0027 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4688G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 4688 | chr10 | 99709371 | ||||||
| chr10:99709472 | T | C | 1 | a0001c0003t0029 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4789T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 4789 | chr10 | 99709472 | ||||||
| chr10:99709597 | T | C | 1 | a0001c0001t0011 | 4 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4914T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 4914 | chr10 | 99709597 | ||||||
| chr10:99709753 | A | G | 1 | a0002c0002t0006 | 12 | HG01243.hp1 HG01358.hp1 HG01496.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5070A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 5070 | chr10 | 99709753 | ||||||
| chr10:99709796 | T | C | 1 | a0001c0001t0015 | 2 | HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5113T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 5113 | chr10 | 99709796 | ||||||
| chr10:99709848 | G | A | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
3_prime_UTR_variant | MODIFIER | c.*5165G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 5165 | chr10 | 99709848 | ||||||
| chr10:99709850 | G | A | 1 | a0001c0001t0015 | 2 | HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5167G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 5167 | chr10 | 99709850 | ||||||
| chr10:99710146 | T | G | 3 | a0001c0001t0004 a0001c0001t0020 a0001c0001t0043 |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*5463T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 5463 | chr10 | 99710146 | ||||||
| chr10:99710328 | C | A | 1 | a0001c0001t0007 | 10 | HG00423.hp2 HG00621.hp1 HG02004.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5645C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 5645 | chr10 | 99710328 | ||||||
| chr10:99710420 | G | A | 1 | a0001c0001t0035 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5737G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 5737 | chr10 | 99710420 | ||||||
| chr10:99710572 | A | G | 1 | a0001c0001t0015 | 2 | HG02630.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5889A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 5889 | chr10 | 99710572 | ||||||
| chr10:99710713 | G | A | 1 | a0001c0001t0017 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6030G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 6030 | chr10 | 99710713 | ||||||
| chr10:99710774 | A | C | 1 | a0001c0001t0042 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6091A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 6091 | chr10 | 99710774 | ||||||
| chr10:99711101 | C | CA | 40 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(37): Show |
326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
3_prime_UTR_variant | MODIFIER | c.*6426dupA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 6427 | INFO_REALIGN_3_PRIME | chr10 | 99711101 | |||||
| chr10:99711142 | A | G | 1 | a0002c0002t0031 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6459A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 6459 | chr10 | 99711142 | ||||||
| chr10:99711166 | T | C | 1 | a0002c0002t0030 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6483T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 6483 | chr10 | 99711166 | ||||||
| chr10:99711170 | A | G | 7 | a0001c0001t0002 a0001c0001t0016 a0001c0001t0021 others(4): Show |
76 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*6487A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 13/13 | 6487 | chr10 | 99711170 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:99659621 | G | A | 5 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(2): Show |
5 | HG02723.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-96+33G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 1/12 | chr10 | 99659621 | |||||||
| chr10:99659623 | A | T | 119 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(116): Show |
140 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.-96+35A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 1/12 | chr10 | 99659623 | |||||||
| chr10:99660027 | G | A | 2 | a0002c0002t0001g0051 a0002c0002t0001g0052 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.8+63G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660027 | |||||||
| chr10:99660028 | C | G | 2 | a0001c0001t0005g0044 a0001c0001t0005g0045 |
4 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.8+64C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660028 | |||||||
| chr10:99660087 | G | T | 1 | a0001c0001t0002g0208 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.8+123G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660087 | |||||||
| chr10:99660351 | G | A | 1 | a0002c0002t0001g0053 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.8+387G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660351 | |||||||
| chr10:99660403 | TA | T | 42 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(39): Show |
58 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.8+445delA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 99660403 | ||||||
| chr10:99660427 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.8+463A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660427 | |||||||
| chr10:99660526 | G | GCA | 9 | a0001c0001t0003g0209 a0001c0001t0003g0210 a0001c0001t0003g0211 others(6): Show |
9 | HG01070.hp2 HG01943.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.8+597_8+598dupCA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 99660526 | ||||||
| chr10:99660526 | GCA | G | 32 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0041 others(29): Show |
39 | HG00423.hp2 HG00621.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.8+597_8+598delCA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 99660526 | ||||||
| chr10:99660526 | GCACA | G | 84 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(81): Show |
104 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.8+595_8+598delCACA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 99660526 | ||||||
| chr10:99660526 | GCACACA | G | 96 | a0001c0001t0002g0008 a0001c0001t0002g0174 a0001c0001t0002g0175 others(93): Show |
132 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.8+593_8+598delCACA others(2): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 99660526 | ||||||
| chr10:99660526 | GCACACAC others(1): Show |
G | 52 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0016 others(49): Show |
70 | HG00140.hp1 HG00423.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.8+591_8+598delCACA others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 99660526 | ||||||
| chr10:99660526 | GCACACAC others(3): Show |
G | 3 | a0001c0001t0002g0207 a0001c0001t0015g0037 a0001c0001t0032g0166 |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.8+589_8+598delCACA others(6): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 99660526 | ||||||
| chr10:99660526 | GCACACAC others(7): Show |
G | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.8+585_8+598delCACA others(10): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 99660526 | ||||||
| chr10:99660532 | A | G | 1 | a0003c0004t0008g0168 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.8+568A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660532 | |||||||
| chr10:99660534 | A | G | 7 | a0001c0001t0003g0311 a0001c0005t0008g0005 a0002c0002t0001g0053 others(4): Show |
11 | HG01123.hp1 HG01261.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.8+570A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660534 | |||||||
| chr10:99660557 | C | G | 1 | a0002c0002t0001g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.8+593C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660557 | |||||||
| chr10:99660559 | C | G | 74 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0021g0206 others(71): Show |
99 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.8+595C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660559 | |||||||
| chr10:99660561 | C | G | 138 | a0001c0001t0001g0094 a0001c0001t0001g0172 a0001c0001t0001g0173 others(135): Show |
185 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.8+597C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660561 | |||||||
| chr10:99660567 | T | G | 56 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(53): Show |
77 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.8+603T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660567 | |||||||
| chr10:99660879 | G | A | 4 | a0001c0001t0005g0042 a0001c0001t0005g0248 a0001c0001t0005g0268 others(1): Show |
5 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.9-567G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660879 | |||||||
| chr10:99660921 | C | CA | 9 | a0001c0001t0002g0179 a0001c0001t0004g0066 a0001c0001t0004g0067 others(6): Show |
11 | HG02451.hp1 HG02630.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.9-511dupA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 99660921 | ||||||
| chr10:99660921 | CA | C | 118 | a0001c0001t0002g0205 a0001c0001t0003g0012 a0001c0001t0003g0017 others(115): Show |
139 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.9-511delA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr10 | 99660921 | ||||||
| chr10:99660958 | T | C | 73 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(70): Show |
87 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.9-488T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99660958 | |||||||
| chr10:99661227 | C | T | 1 | a0001c0001t0011g0247 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.9-219C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 2/12 | chr10 | 99661227 | |||||||
| chr10:99661695 | G | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+67G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99661695 | |||||||
| chr10:99661793 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.191+165G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99661793 | |||||||
| chr10:99661828 | A | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+200A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99661828 | |||||||
| chr10:99661829 | T | A | 4 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(1): Show |
4 | HG02055.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+201T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99661829 | |||||||
| chr10:99662400 | G | A | 1 | a0001c0001t0003g0218 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.191+772G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99662400 | |||||||
| chr10:99662447 | T | TACTTTCA others(15): Show |
1 | a0001c0001t0005g0274 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.191+840_191+841ins others(22): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99662447 | ||||||
| chr10:99662519 | C | T | 2 | a0001c0001t0003g0266 a0001c0001t0003g0267 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.191+891C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99662519 | |||||||
| chr10:99662666 | AAACCAAA others(5): Show |
A | 261 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(258): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.191+1040_191+1051d others(14): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99662666 | ||||||
| chr10:99662718 | A | C | 5 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(2): Show |
5 | HG02723.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.191+1090A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99662718 | |||||||
| chr10:99662739 | G | A | 70 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(67): Show |
95 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.191+1111G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99662739 | |||||||
| chr10:99662764 | A | G | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+1136A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99662764 | |||||||
| chr10:99662764 | A | T | 1 | a0001c0001t0002g0177 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.191+1136A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99662764 | |||||||
| chr10:99663159 | G | C | 1 | a0001c0001t0004g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.191+1531G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663159 | |||||||
| chr10:99663174 | C | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+1546C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663174 | |||||||
| chr10:99663200 | T | C | 1 | a0002c0002t0006g0109 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.191+1572T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663200 | |||||||
| chr10:99663465 | G | GT | 48 | a0001c0001t0002g0164 a0001c0001t0003g0040 a0001c0001t0003g0215 others(45): Show |
57 | HG00280.hp1 HG00609.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.191+1852dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99663465 | ||||||
| chr10:99663465 | G | GTT | 6 | a0001c0001t0005g0301 a0001c0001t0005g0302 a0001c0001t0005g0303 others(3): Show |
6 | HG01081.hp2 HG02717.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+1851_191+1852d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99663465 | ||||||
| chr10:99663465 | G | T | 1 | a0001c0001t0003g0216 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.191+1837G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663465 | |||||||
| chr10:99663489 | C | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+1861C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663489 | |||||||
| chr10:99663493 | C | T | 2 | a0001c0001t0010g0026 a0001c0001t0010g0108 |
3 | HG00639.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.191+1865C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663493 | |||||||
| chr10:99663564 | A | G | 1 | a0001c0001t0007g0265 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.191+1936A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663564 | |||||||
| chr10:99663700 | A | G | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+2072A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663700 | |||||||
| chr10:99663873 | T | C | 1 | a0001c0001t0005g0277 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.191+2245T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663873 | |||||||
| chr10:99663938 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0036 |
4 | HG00741.hp2 HG01081.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.191+2310A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663938 | |||||||
| chr10:99663993 | A | G | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+2365A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99663993 | |||||||
| chr10:99664245 | A | G | 1 | a0001c0001t0003g0243 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.191+2617A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99664245 | |||||||
| chr10:99664324 | G | T | 8 | a0001c0001t0002g0009 a0001c0001t0002g0199 a0001c0001t0002g0200 others(5): Show |
12 | HG00423.hp1 HG02273.hp1 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.191+2696G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99664324 | |||||||
| chr10:99664450 | C | CT | 7 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0003g0242 others(4): Show |
7 | HG00741.hp1 HG02071.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+2839dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99664450 | ||||||
| chr10:99664557 | C | T | 1 | a0001c0001t0003g0264 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.191+2929C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99664557 | |||||||
| chr10:99664705 | T | C | 2 | a0001c0001t0002g0174 a0001c0001t0002g0175 |
2 | NA18984.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.191+3077T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99664705 | |||||||
| chr10:99664973 | G | A | 1 | a0001c0001t0032g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.191+3345G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99664973 | |||||||
| chr10:99665028 | A | G | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+3400A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665028 | |||||||
| chr10:99665119 | G | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+3491G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665119 | |||||||
| chr10:99665244 | C | A | 1 | a0001c0001t0041g0095 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.191+3616C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665244 | |||||||
| chr10:99665256 | G | GA | 257 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(254): Show |
326 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.191+3641dupA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99665256 | ||||||
| chr10:99665256 | GA | G | 4 | a0001c0001t0015g0037 a0001c0005t0008g0005 a0003c0004t0008g0005 others(1): Show |
9 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.191+3641delA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99665256 | ||||||
| chr10:99665258 | A | G | 1 | a0001c0001t0032g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.191+3630A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665258 | |||||||
| chr10:99665440 | G | A | 5 | a0001c0001t0004g0070 a0001c0001t0004g0071 a0001c0001t0004g0072 others(2): Show |
5 | HG02056.hp2 HG02155.hp2 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.191+3812G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665440 | |||||||
| chr10:99665476 | G | T | 1 | a0002c0002t0001g0151 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.191+3848G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665476 | |||||||
| chr10:99665521 | A | ATCAT | 8 | a0001c0001t0004g0011 a0001c0001t0004g0024 a0001c0001t0004g0068 others(5): Show |
12 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.191+3909_191+3912d others(6): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99665521 | ||||||
| chr10:99665619 | C | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+3991C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665619 | |||||||
| chr10:99665711 | C | T | 265 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(262): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.191+4083C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665711 | |||||||
| chr10:99665715 | A | G | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.191+4087A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665715 | |||||||
| chr10:99665746 | G | T | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+4118G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665746 | |||||||
| chr10:99665821 | A | C | 261 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(258): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.191+4193A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99665821 | |||||||
| chr10:99666000 | A | T | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+4372A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666000 | |||||||
| chr10:99666256 | G | A | 70 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0007 others(67): Show |
95 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.191+4628G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666256 | |||||||
| chr10:99666256 | G | T | 1 | a0001c0001t0007g0263 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.191+4628G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666256 | |||||||
| chr10:99666268 | C | T | 1 | a0001c0001t0017g0025 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.191+4640C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666268 | |||||||
| chr10:99666294 | G | A | 3 | a0001c0001t0005g0278 a0001c0001t0005g0279 a0001c0001t0005g0280 |
3 | NA18985.hp1 NA19056.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.191+4666G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666294 | |||||||
| chr10:99666361 | C | T | 1 | a0001c0001t0036g0300 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.191+4733C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666361 | |||||||
| chr10:99666502 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.191+4874C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666502 | |||||||
| chr10:99666571 | G | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+4943G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666571 | |||||||
| chr10:99666610 | C | A | 4 | a0001c0001t0012g0015 a0001c0001t0012g0096 a0001c0001t0041g0095 others(1): Show |
6 | HG02451.hp1 HG02630.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+4982C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666610 | |||||||
| chr10:99666755 | C | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+5127C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666755 | |||||||
| chr10:99666770 | A | G | 262 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(259): Show |
332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.191+5142A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666770 | |||||||
| chr10:99666944 | G | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02818.hp1 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.191+5316G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99666944 | |||||||
| chr10:99667293 | A | G | 261 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(258): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.191+5665A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99667293 | |||||||
| chr10:99667396 | G | T | 1 | a0001c0001t0012g0015 | 3 | HG02630.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.191+5768G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99667396 | |||||||
| chr10:99667435 | T | G | 1 | a0001c0001t0002g0181 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.191+5807T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99667435 | |||||||
| chr10:99667590 | C | T | 2 | a0001c0001t0018g0261 a0001c0001t0018g0262 |
2 | HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.191+5962C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99667590 | |||||||
| chr10:99667893 | A | C | 1 | a0002c0002t0001g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.191+6265A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99667893 | |||||||
| chr10:99667929 | C | CT | 175 | a0001c0001t0001g0094 a0001c0001t0001g0172 a0001c0001t0001g0173 others(172): Show |
218 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.191+6324dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99667929 | ||||||
| chr10:99667929 | C | CTT | 74 | a0001c0001t0001g0092 a0001c0001t0002g0039 a0001c0001t0002g0163 others(71): Show |
100 | HG00438.hp1 HG00642.hp2 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.191+6323_191+6324d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99667929 | ||||||
| chr10:99667929 | C | CTTT | 6 | a0002c0002t0001g0149 a0002c0002t0001g0150 a0002c0002t0001g0153 others(3): Show |
6 | HG00558.hp1 HG01261.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.191+6322_191+6324d others(5): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99667929 | ||||||
| chr10:99668052 | A | G | 261 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(258): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.191+6424A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668052 | |||||||
| chr10:99668082 | G | A | 73 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(70): Show |
87 | HG00099.hp2 HG00423.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.191+6454G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668082 | |||||||
| chr10:99668096 | G | A | 4 | a0001c0001t0012g0015 a0001c0001t0012g0096 a0001c0001t0041g0095 others(1): Show |
6 | HG02451.hp1 HG02630.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.191+6468G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668096 | |||||||
| chr10:99668226 | T | C | 265 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(262): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.191+6598T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668226 | |||||||
| chr10:99668231 | G | A | 1 | a0001c0001t0018g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.191+6603G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668231 | |||||||
| chr10:99668307 | G | A | 1 | a0002c0002t0001g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.191+6679G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668307 | |||||||
| chr10:99668343 | A | G | 1 | a0001c0001t0042g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.191+6715A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668343 | |||||||
| chr10:99668346 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.191+6718C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668346 | |||||||
| chr10:99668383 | A | T | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.191+6755A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668383 | |||||||
| chr10:99668430 | T | G | 1 | a0001c0001t0007g0222 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.191+6802T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668430 | |||||||
| chr10:99668589 | G | C | 1 | a0001c0001t0003g0223 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.191+6961G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668589 | |||||||
| chr10:99668675 | A | G | 2 | a0001c0001t0010g0026 a0001c0001t0010g0108 |
3 | HG00639.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.191+7047A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668675 | |||||||
| chr10:99668782 | G | C | 2 | a0001c0001t0012g0015 a0001c0001t0012g0096 |
4 | HG02630.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.191+7154G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668782 | |||||||
| chr10:99668826 | T | A | 58 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
80 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.191+7198T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99668826 | |||||||
| chr10:99669010 | A | C | 1 | a0001c0001t0004g0090 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.191+7382A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669010 | |||||||
| chr10:99669042 | C | CT | 47 | a0001c0001t0002g0195 a0001c0001t0002g0203 a0001c0001t0003g0223 others(44): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.191+7430dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99669042 | ||||||
| chr10:99669085 | C | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+7457C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669085 | |||||||
| chr10:99669090 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02818.hp1 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.191+7462G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669090 | |||||||
| chr10:99669366 | A | G | 52 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(49): Show |
73 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.191+7738A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669366 | |||||||
| chr10:99669386 | T | G | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.191+7758T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669386 | |||||||
| chr10:99669579 | A | T | 1 | a0002c0002t0001g0031 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.191+7951A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669579 | |||||||
| chr10:99669707 | G | A | 1 | a0002c0002t0006g0110 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.191+8079G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669707 | |||||||
| chr10:99669740 | G | GT | 150 | a0001c0001t0001g0092 a0001c0001t0002g0001 a0001c0001t0002g0008 others(147): Show |
185 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.191+8139dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99669740 | ||||||
| chr10:99669740 | G | GTT | 81 | a0001c0001t0002g0036 a0001c0001t0002g0176 a0001c0001t0002g0180 others(78): Show |
99 | HG00558.hp2 HG00609.hp1 HG00673.hp2 others(96): Show |
intron_variant | MODIFIER | c.191+8138_191+8139d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99669740 | ||||||
| chr10:99669740 | G | GTTT | 21 | a0001c0001t0012g0096 a0001c0001t0042g0097 a0002c0002t0001g0004 others(18): Show |
25 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.191+8137_191+8139d others(5): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99669740 | ||||||
| chr10:99669740 | G | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.191+8112G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669740 | |||||||
| chr10:99669765 | T | G | 1 | a0001c0001t0004g0021 | 2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.191+8137T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669765 | |||||||
| chr10:99669783 | T | C | 3 | a0001c0001t0012g0015 a0001c0001t0012g0096 a0001c0001t0042g0097 |
5 | HG02630.hp1 HG03139.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.191+8155T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669783 | |||||||
| chr10:99669819 | G | A | 1 | a0001c0001t0003g0210 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.191+8191G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669819 | |||||||
| chr10:99669836 | G | A | 78 | a0001c0001t0010g0106 a0001c0001t0017g0025 a0001c0003t0001g0101 others(75): Show |
104 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.191+8208G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669836 | |||||||
| chr10:99669842 | C | T | 1 | a0001c0001t0010g0026 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.191+8214C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669842 | |||||||
| chr10:99669939 | C | T | 1 | a0002c0002t0001g0139 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.191+8311C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99669939 | |||||||
| chr10:99670089 | A | G | 1 | a0002c0002t0001g0138 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.191+8461A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99670089 | |||||||
| chr10:99670126 | A | G | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.191+8498A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99670126 | |||||||
| chr10:99670281 | T | C | 142 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(139): Show |
190 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.191+8653T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99670281 | |||||||
| chr10:99670423 | T | C | 1 | a0006c0012t0002g0178 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.191+8795T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99670423 | |||||||
| chr10:99670457 | G | A | 3 | a0001c0001t0004g0073 a0001c0001t0004g0078 a0001c0001t0004g0085 |
3 | NA18940.hp1 NA18965.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.192-8804G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99670457 | |||||||
| chr10:99670531 | A | G | 1 | a0001c0003t0001g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.192-8730A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99670531 | |||||||
| chr10:99670562 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.192-8699C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99670562 | |||||||
| chr10:99670638 | A | G | 1 | a0001c0001t0037g0256 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.192-8623A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99670638 | |||||||
| chr10:99670907 | A | T | 1 | a0001c0001t0002g0201 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.192-8354A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99670907 | |||||||
| chr10:99671051 | T | G | 1 | a0001c0001t0004g0070 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.192-8210T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671051 | |||||||
| chr10:99671124 | G | A | 1 | a0001c0001t0009g0082 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.192-8137G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671124 | |||||||
| chr10:99671154 | A | C | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.192-8107A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671154 | |||||||
| chr10:99671195 | A | T | 1 | a0002c0002t0013g0137 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.192-8066A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671195 | |||||||
| chr10:99671227 | A | G | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-8034A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671227 | |||||||
| chr10:99671228 | T | C | 2 | a0001c0001t0005g0276 a0001c0001t0005g0307 |
2 | HG00738.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.192-8033T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671228 | |||||||
| chr10:99671251 | G | C | 1 | a0001c0001t0042g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.192-8010G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671251 | |||||||
| chr10:99671432 | AT | A | 40 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0040 others(37): Show |
46 | HG00099.hp2 HG00639.hp1 HG01070.hp2 others(43): Show |
intron_variant | MODIFIER | c.192-7826delT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99671432 | ||||||
| chr10:99671475 | C | T | 4 | a0001c0001t0012g0015 a0001c0001t0012g0096 a0001c0001t0041g0095 others(1): Show |
6 | HG02451.hp1 HG02630.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-7786C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671475 | |||||||
| chr10:99671813 | G | A | 1 | a0001c0001t0003g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.192-7448G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671813 | |||||||
| chr10:99671822 | T | C | 2 | a0002c0002t0001g0118 a0002c0002t0001g0140 |
2 | HG03654.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.192-7439T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671822 | |||||||
| chr10:99671982 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.192-7279A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99671982 | |||||||
| chr10:99672011 | G | A | 2 | a0001c0001t0003g0253 a0001c0001t0003g0254 |
2 | HG02258.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.192-7250G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99672011 | |||||||
| chr10:99672288 | A | G | 2 | a0001c0003t0001g0101 a0005c0007t0001g0105 |
2 | HG02486.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.192-6973A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99672288 | |||||||
| chr10:99672307 | C | CT | 142 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(139): Show |
191 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.192-6939dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99672307 | ||||||
| chr10:99672466 | C | T | 51 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
72 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.192-6795C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99672466 | |||||||
| chr10:99672560 | C | A | 1 | a0001c0001t0005g0044 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.192-6701C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99672560 | |||||||
| chr10:99672835 | C | T | 2 | a0001c0001t0005g0294 a0001c0001t0038g0293 |
2 | HG02818.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.192-6426C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99672835 | |||||||
| chr10:99673029 | T | C | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.192-6232T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99673029 | |||||||
| chr10:99673340 | A | G | 1 | a0001c0001t0003g0306 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.192-5921A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99673340 | |||||||
| chr10:99673344 | G | A | 1 | a0001c0001t0039g0305 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.192-5917G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99673344 | |||||||
| chr10:99673495 | A | T | 1 | a0001c0001t0002g0189 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.192-5766A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99673495 | |||||||
| chr10:99673635 | G | A | 261 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(258): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.192-5626G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99673635 | |||||||
| chr10:99673804 | T | C | 1 | a0001c0001t0003g0253 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.192-5457T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99673804 | |||||||
| chr10:99673915 | G | C | 265 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(262): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.192-5346G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99673915 | |||||||
| chr10:99674012 | CAG | C | 142 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(139): Show |
190 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(187): Show |
intron_variant | MODIFIER | c.192-5248_192-5247d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674012 | |||||||
| chr10:99674026 | G | A | 1 | a0001c0001t0002g0179 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.192-5235G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674026 | |||||||
| chr10:99674093 | T | C | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.192-5168T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674093 | |||||||
| chr10:99674123 | C | G | 1 | a0001c0003t0001g0160 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.192-5138C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674123 | |||||||
| chr10:99674125 | T | C | 2 | a0001c0001t0002g0182 a0001c0001t0002g0208 |
2 | NA18948.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.192-5136T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674125 | |||||||
| chr10:99674168 | G | T | 1 | a0001c0001t0005g0269 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.192-5093G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674168 | |||||||
| chr10:99674401 | A | C | 56 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(53): Show |
77 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.192-4860A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674401 | |||||||
| chr10:99674584 | C | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.192-4677C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674584 | |||||||
| chr10:99674607 | G | C | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.192-4654G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674607 | |||||||
| chr10:99674811 | C | T | 1 | a0001c0001t0005g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.192-4450C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674811 | |||||||
| chr10:99674840 | T | C | 1 | a0001c0001t0005g0302 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.192-4421T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674840 | |||||||
| chr10:99674963 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02818.hp1 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.192-4298A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99674963 | |||||||
| chr10:99675247 | A | G | 1 | a0001c0001t0005g0292 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.192-4014A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99675247 | |||||||
| chr10:99675366 | G | A | 265 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(262): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.192-3895G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99675366 | |||||||
| chr10:99675398 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.192-3863A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99675398 | |||||||
| chr10:99675459 | T | C | 4 | a0001c0001t0012g0015 a0001c0001t0012g0096 a0001c0001t0041g0095 others(1): Show |
6 | HG02451.hp1 HG02630.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-3802T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99675459 | |||||||
| chr10:99675553 | T | G | 1 | a0002c0002t0001g0142 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.192-3708T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99675553 | |||||||
| chr10:99675554 | A | G | 262 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(259): Show |
332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.192-3707A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99675554 | |||||||
| chr10:99675597 | A | AT | 251 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(248): Show |
319 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.192-3647dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99675597 | ||||||
| chr10:99675597 | A | ATT | 6 | a0001c0001t0002g0197 a0001c0001t0010g0026 a0001c0001t0010g0108 others(3): Show |
7 | HG00639.hp2 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-3648_192-3647d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99675597 | ||||||
| chr10:99676109 | C | T | 1 | a0001c0001t0003g0215 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.192-3152C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99676109 | |||||||
| chr10:99676366 | A | G | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-2895A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99676366 | |||||||
| chr10:99676408 | C | T | 262 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(259): Show |
332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.192-2853C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99676408 | |||||||
| chr10:99676961 | G | A | 119 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(116): Show |
140 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.192-2300G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99676961 | |||||||
| chr10:99677000 | A | G | 2 | a0001c0001t0004g0073 a0001c0001t0004g0078 |
2 | NA18965.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.192-2261A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99677000 | |||||||
| chr10:99677052 | G | A | 4 | a0001c0001t0012g0015 a0001c0001t0012g0096 a0001c0001t0041g0095 others(1): Show |
6 | HG02451.hp1 HG02630.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.192-2209G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99677052 | |||||||
| chr10:99677085 | A | G | 1 | a0001c0001t0004g0069 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.192-2176A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99677085 | |||||||
| chr10:99677087 | T | C | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.192-2174T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99677087 | |||||||
| chr10:99677148 | T | C | 262 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(259): Show |
332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.192-2113T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99677148 | |||||||
| chr10:99677295 | T | C | 1 | a0001c0001t0005g0283 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.192-1966T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99677295 | |||||||
| chr10:99677359 | C | CT | 56 | a0001c0001t0002g0182 a0001c0001t0002g0188 a0001c0001t0002g0194 others(53): Show |
65 | HG00099.hp2 HG00639.hp1 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.192-1879dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99677359 | ||||||
| chr10:99677359 | CT | C | 31 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0213 others(28): Show |
41 | HG00423.hp2 HG00621.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.192-1879delT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99677359 | ||||||
| chr10:99677396 | G | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.192-1865G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99677396 | |||||||
| chr10:99677420 | A | G | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.192-1841A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99677420 | |||||||
| chr10:99677657 | G | A | 5 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0001c0001t0002g0188 others(2): Show |
5 | NA18953.hp2 NA18967.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.192-1604G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99677657 | |||||||
| chr10:99677714 | A | C | 1 | a0002c0002t0001g0154 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.192-1547A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99677714 | |||||||
| chr10:99678041 | G | T | 3 | a0001c0001t0010g0106 a0001c0001t0017g0025 a0001c0001t0032g0166 |
4 | HG02451.hp2 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-1220G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678041 | |||||||
| chr10:99678111 | G | A | 3 | a0001c0001t0010g0106 a0001c0001t0017g0025 a0001c0001t0032g0166 |
4 | HG02451.hp2 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-1150G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678111 | |||||||
| chr10:99678201 | G | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.192-1060G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678201 | |||||||
| chr10:99678250 | C | T | 1 | a0002c0002t0001g0134 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.192-1011C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678250 | |||||||
| chr10:99678265 | G | A | 141 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(138): Show |
189 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.192-996G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678265 | |||||||
| chr10:99678284 | C | T | 1 | a0001c0001t0004g0076 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.192-977C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678284 | |||||||
| chr10:99678328 | C | T | 1 | a0001c0001t0004g0085 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.192-933C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678328 | |||||||
| chr10:99678360 | T | C | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.192-901T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678360 | |||||||
| chr10:99678423 | A | G | 269 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(266): Show |
345 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.192-838A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678423 | |||||||
| chr10:99678494 | T | TA | 3 | a0001c0001t0010g0106 a0001c0001t0017g0025 a0001c0001t0032g0166 |
4 | HG02451.hp2 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.192-766dupA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99678494 | ||||||
| chr10:99678632 | C | G | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.192-629C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678632 | |||||||
| chr10:99678732 | G | A | 2 | a0001c0001t0010g0106 a0001c0001t0017g0025 |
3 | HG02451.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.192-529G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678732 | |||||||
| chr10:99678776 | C | CA | 258 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(255): Show |
327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.192-470dupA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr10 | 99678776 | ||||||
| chr10:99678807 | T | A | 269 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(266): Show |
345 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.192-454T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678807 | |||||||
| chr10:99678967 | A | G | 1 | a0001c0001t0004g0059 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.192-294A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678967 | |||||||
| chr10:99678988 | A | T | 1 | a0002c0002t0001g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.192-273A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 3/12 | chr10 | 99678988 | |||||||
| chr10:99679495 | G | A | 265 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(262): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.397+29G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 4/12 | chr10 | 99679495 | |||||||
| chr10:99679984 | T | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.548+109T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99679984 | |||||||
| chr10:99680247 | G | A | 1 | a0001c0001t0005g0310 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.548+372G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99680247 | |||||||
| chr10:99680589 | T | A | 1 | a0001c0001t0005g0279 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.548+714T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99680589 | |||||||
| chr10:99680627 | C | T | 2 | a0001c0001t0005g0274 a0001c0001t0005g0275 |
2 | HG03654.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.548+752C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99680627 | |||||||
| chr10:99680638 | G | A | 31 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0024 others(28): Show |
39 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.548+763G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99680638 | |||||||
| chr10:99680833 | T | C | 1 | a0002c0002t0001g0119 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.548+958T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99680833 | |||||||
| chr10:99681191 | A | C | 2 | a0001c0001t0003g0266 a0001c0001t0003g0267 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.548+1316A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99681191 | |||||||
| chr10:99681213 | A | G | 1 | a0001c0001t0002g0048 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.548+1338A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99681213 | |||||||
| chr10:99681267 | A | ATTAT | 130 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(127): Show |
176 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.548+1416_548+1419d others(6): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 99681267 | ||||||
| chr10:99681267 | A | ATTATTTA others(1): Show |
13 | a0001c0001t0002g0187 a0001c0001t0005g0289 a0001c0001t0005g0298 others(10): Show |
15 | HG02135.hp1 HG02165.hp1 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.548+1412_548+1419d others(10): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 99681267 | ||||||
| chr10:99681300 | A | T | 1 | a0001c0001t0004g0067 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.548+1425A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99681300 | |||||||
| chr10:99681310 | G | A | 1 | a0002c0002t0001g0122 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.548+1435G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99681310 | |||||||
| chr10:99681364 | C | T | 1 | a0002c0002t0001g0145 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.548+1489C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99681364 | |||||||
| chr10:99681464 | G | C | 1 | a0001c0001t0003g0219 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.548+1589G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99681464 | |||||||
| chr10:99681558 | A | G | 1 | a0001c0001t0024g0245 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.548+1683A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99681558 | |||||||
| chr10:99682132 | T | C | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | NA19007.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.548+2257T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99682132 | |||||||
| chr10:99682199 | G | GT | 264 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(261): Show |
338 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.548+2339dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 99682199 | ||||||
| chr10:99682213 | T | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.548+2338T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99682213 | |||||||
| chr10:99682214 | T | C | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.548+2339T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99682214 | |||||||
| chr10:99682398 | T | C | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.548+2523T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99682398 | |||||||
| chr10:99682421 | C | T | 1 | a0002c0002t0001g0102 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.548+2546C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99682421 | |||||||
| chr10:99682764 | G | A | 1 | a0001c0001t0016g0033 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.548+2889G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99682764 | |||||||
| chr10:99682830 | G | A | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.548+2955G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99682830 | |||||||
| chr10:99682971 | C | A | 1 | a0001c0001t0004g0074 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.549-2821C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99682971 | |||||||
| chr10:99683577 | C | T | 1 | a0001c0001t0004g0058 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.549-2215C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99683577 | |||||||
| chr10:99683767 | G | GA | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.549-2024dupA | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr10 | 99683767 | ||||||
| chr10:99683912 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.549-1880A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99683912 | |||||||
| chr10:99684093 | T | A | 9 | a0001c0001t0003g0012 a0001c0001t0003g0210 a0001c0001t0003g0216 others(6): Show |
12 | HG02155.hp1 NA18945.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.549-1699T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99684093 | |||||||
| chr10:99684181 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.549-1611G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99684181 | |||||||
| chr10:99684240 | T | C | 261 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(258): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.549-1552T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99684240 | |||||||
| chr10:99684288 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.549-1504G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99684288 | |||||||
| chr10:99684533 | T | C | 1 | a0002c0002t0001g0133 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.549-1259T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99684533 | |||||||
| chr10:99684536 | A | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0142 |
3 | HG01975.hp2 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.549-1256A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99684536 | |||||||
| chr10:99684537 | C | G | 2 | a0002c0002t0001g0029 a0002c0002t0001g0142 |
3 | HG01975.hp2 HG02148.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.549-1255C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99684537 | |||||||
| chr10:99684608 | G | C | 119 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(116): Show |
140 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.549-1184G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99684608 | |||||||
| chr10:99684983 | C | G | 2 | a0002c0002t0001g0123 a0002c0002t0001g0124 |
2 | NA19007.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.549-809C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99684983 | |||||||
| chr10:99685087 | G | A | 47 | a0001c0001t0005g0010 a0001c0001t0005g0042 a0001c0001t0005g0043 others(44): Show |
54 | HG00280.hp1 HG00609.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.549-705G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99685087 | |||||||
| chr10:99685121 | G | A | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549-671G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99685121 | |||||||
| chr10:99685434 | A | T | 1 | a0001c0001t0039g0305 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.549-358A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99685434 | |||||||
| chr10:99685460 | G | T | 1 | a0001c0003t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.549-332G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99685460 | |||||||
| chr10:99685566 | G | C | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.549-226G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 5/12 | chr10 | 99685566 | |||||||
| chr10:99685951 | C | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.652+56C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99685951 | |||||||
| chr10:99686087 | G | A | 1 | a0002c0002t0001g0125 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.652+192G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99686087 | |||||||
| chr10:99686145 | G | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.652+250G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99686145 | |||||||
| chr10:99686190 | G | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.652+295G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99686190 | |||||||
| chr10:99686353 | TAATTCCC others(3): Show |
T | 1 | a0002c0002t0001g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.652+462_652+471del others(10): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 99686353 | ||||||
| chr10:99686579 | T | G | 2 | a0001c0001t0003g0216 a0001c0001t0003g0229 |
2 | HG02155.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.652+684T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99686579 | |||||||
| chr10:99686622 | C | G | 1 | a0001c0001t0032g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.652+727C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99686622 | |||||||
| chr10:99686623 | TTTCCATT others(16): Show |
T | 1 | a0002c0002t0001g0114 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.652+729_652+751del others(23): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99686623 | |||||||
| chr10:99686635 | G | T | 1 | a0001c0001t0004g0021 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.652+740G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99686635 | |||||||
| chr10:99686850 | C | CT | 5 | a0001c0001t0004g0089 a0001c0001t0015g0037 a0001c0005t0008g0005 others(2): Show |
10 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.652+966dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 99686850 | ||||||
| chr10:99686916 | CT | C | 255 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(252): Show |
325 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.652+1040delT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 99686916 | ||||||
| chr10:99687125 | C | A | 1 | a0001c0001t0038g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.652+1230C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687125 | |||||||
| chr10:99687150 | C | T | 4 | a0001c0001t0002g0038 a0001c0001t0002g0181 a0001c0001t0002g0192 others(1): Show |
5 | HG02027.hp2 HG02056.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.652+1255C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687150 | |||||||
| chr10:99687197 | A | G | 269 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(266): Show |
345 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.652+1302A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687197 | |||||||
| chr10:99687229 | T | C | 1 | a0001c0001t0038g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.652+1334T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687229 | |||||||
| chr10:99687234 | T | C | 1 | a0001c0001t0038g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.652+1339T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687234 | |||||||
| chr10:99687259 | C | CT | 48 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0014 others(45): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.652+1389dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 99687259 | ||||||
| chr10:99687259 | C | CTT | 8 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0085 others(5): Show |
12 | HG00621.hp2 HG02109.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.652+1388_652+1389d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 99687259 | ||||||
| chr10:99687259 | C | CTTTCTT | 105 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(102): Show |
121 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.652+1367_652+1368i others(8): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 99687259 | ||||||
| chr10:99687259 | C | CTTTCTTT | 34 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(31): Show |
42 | HG00423.hp1 HG00639.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.652+1367_652+1368i others(9): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 99687259 | ||||||
| chr10:99687259 | C | CTTTCTTT others(1): Show |
94 | a0001c0001t0001g0092 a0001c0001t0002g0001 a0001c0001t0002g0008 others(91): Show |
123 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.652+1367_652+1368i others(10): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 99687259 | ||||||
| chr10:99687259 | C | CTTTCTTT others(2): Show |
28 | a0001c0001t0001g0094 a0001c0001t0001g0173 a0001c0001t0002g0001 others(25): Show |
32 | HG00140.hp1 HG00642.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.652+1367_652+1368i others(11): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 99687259 | ||||||
| chr10:99687259 | C | CTTTCTTT others(3): Show |
4 | a0001c0001t0001g0172 a0001c0001t0027g0001 a0002c0002t0001g0007 others(1): Show |
4 | HG01261.hp1 HG02886.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.652+1367_652+1368i others(12): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr10 | 99687259 | ||||||
| chr10:99687296 | T | C | 1 | a0001c0001t0038g0293 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.653-1398T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687296 | |||||||
| chr10:99687369 | G | A | 1 | a0001c0001t0005g0304 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.653-1325G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687369 | |||||||
| chr10:99687372 | T | A | 1 | a0001c0001t0003g0230 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.653-1322T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687372 | |||||||
| chr10:99687373 | C | T | 1 | a0001c0001t0003g0230 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.653-1321C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687373 | |||||||
| chr10:99687501 | G | A | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.653-1193G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687501 | |||||||
| chr10:99687650 | T | C | 1 | a0001c0001t0005g0268 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.653-1044T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687650 | |||||||
| chr10:99687765 | G | C | 1 | a0001c0001t0041g0095 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.653-929G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687765 | |||||||
| chr10:99687829 | T | A | 2 | a0001c0001t0003g0223 a0001c0001t0003g0226 |
2 | NA18945.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.653-865T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99687829 | |||||||
| chr10:99688062 | G | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.653-632G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99688062 | |||||||
| chr10:99688224 | G | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.653-470G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99688224 | |||||||
| chr10:99688234 | G | T | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.653-460G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99688234 | |||||||
| chr10:99688254 | T | C | 1 | a0001c0001t0036g0300 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.653-440T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99688254 | |||||||
| chr10:99688518 | T | G | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.653-176T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 6/12 | chr10 | 99688518 | |||||||
| chr10:99688781 | A | G | 3 | a0001c0001t0004g0063 a0001c0001t0004g0064 a0001c0001t0020g0065 |
3 | NA18945.hp2 NA18995.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.709+31A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99688781 | |||||||
| chr10:99688866 | A | G | 1 | a0001c0001t0003g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.709+116A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99688866 | |||||||
| chr10:99688951 | G | A | 1 | a0002c0002t0001g0126 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.709+201G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99688951 | |||||||
| chr10:99689045 | GT | G | 5 | a0001c0001t0003g0019 a0001c0001t0003g0221 a0001c0001t0003g0250 others(2): Show |
7 | HG01109.hp2 HG02559.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.709+304delT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 99689045 | ||||||
| chr10:99689276 | C | T | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.709+526C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99689276 | |||||||
| chr10:99689343 | T | A | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.709+593T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99689343 | |||||||
| chr10:99689399 | A | G | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.709+649A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99689399 | |||||||
| chr10:99689530 | G | A | 1 | a0001c0001t0010g0026 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.709+780G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99689530 | |||||||
| chr10:99689764 | T | A | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.709+1014T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99689764 | |||||||
| chr10:99689804 | A | G | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.709+1054A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99689804 | |||||||
| chr10:99690005 | A | G | 1 | a0003c0004t0008g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.709+1255A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99690005 | |||||||
| chr10:99690107 | G | A | 1 | a0002c0006t0001g0127 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.710-1278G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99690107 | |||||||
| chr10:99690493 | C | T | 57 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(54): Show |
79 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.710-892C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99690493 | |||||||
| chr10:99690546 | A | AT | 81 | a0001c0001t0003g0228 a0001c0001t0004g0062 a0001c0001t0005g0278 others(78): Show |
108 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.710-823dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 99690546 | ||||||
| chr10:99690546 | AT | A | 11 | a0001c0001t0003g0224 a0001c0001t0003g0231 a0001c0001t0004g0089 others(8): Show |
12 | HG01081.hp2 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.710-823delT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr10 | 99690546 | ||||||
| chr10:99690565 | G | C | 1 | a0001c0001t0002g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.710-820G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99690565 | |||||||
| chr10:99690703 | C | T | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.710-682C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99690703 | |||||||
| chr10:99690751 | A | C | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.710-634A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99690751 | |||||||
| chr10:99690827 | C | T | 1 | a0001c0001t0004g0021 | 2 | HG00733.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.710-558C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99690827 | |||||||
| chr10:99690922 | A | C | 1 | a0001c0003t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.710-463A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99690922 | |||||||
| chr10:99690937 | A | G | 262 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(259): Show |
332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.710-448A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99690937 | |||||||
| chr10:99691072 | A | G | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.710-313A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99691072 | |||||||
| chr10:99691161 | A | C | 1 | a0001c0003t0029g0107 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.710-224A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99691161 | |||||||
| chr10:99691163 | A | T | 108 | a0001c0001t0001g0094 a0001c0001t0001g0172 a0001c0001t0001g0173 others(105): Show |
137 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.710-222A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99691163 | |||||||
| chr10:99691164 | T | A | 1 | a0002c0002t0001g0155 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.710-221T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99691164 | |||||||
| chr10:99691221 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.710-164G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99691221 | |||||||
| chr10:99691252 | A | G | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.710-133A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 7/12 | chr10 | 99691252 | |||||||
| chr10:99691596 | A | G | 5 | a0001c0001t0003g0040 a0001c0001t0003g0215 a0001c0001t0003g0232 others(2): Show |
6 | HG01884.hp2 HG02258.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+78A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99691596 | |||||||
| chr10:99691628 | A | T | 1 | a0001c0001t0004g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.843+110A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99691628 | |||||||
| chr10:99691745 | C | T | 3 | a0001c0001t0010g0106 a0001c0001t0017g0025 a0001c0001t0032g0166 |
4 | HG02451.hp2 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+227C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99691745 | |||||||
| chr10:99691747 | A | T | 3 | a0002c0002t0013g0132 a0002c0002t0013g0137 a0002c0002t0013g0144 |
3 | NA19006.hp2 NA19080.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.843+229A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99691747 | |||||||
| chr10:99691749 | G | GTAATATT others(30): Show |
3 | a0002c0002t0013g0132 a0002c0002t0013g0137 a0002c0002t0013g0144 |
3 | NA19006.hp2 NA19080.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.843+232_843+233ins others(37): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 99691749 | ||||||
| chr10:99691789 | A | G | 262 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(259): Show |
332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.843+271A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99691789 | |||||||
| chr10:99691854 | T | C | 76 | a0001c0003t0001g0101 a0001c0003t0001g0158 a0001c0003t0001g0159 others(73): Show |
101 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.843+336T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99691854 | |||||||
| chr10:99692031 | C | CATTATGT others(6): Show |
1 | a0001c0001t0014g0297 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.843+526_843+538dup others(13): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 99692031 | ||||||
| chr10:99692031 | CATTATGT others(6): Show |
C | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.843+526_843+538del others(13): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 99692031 | ||||||
| chr10:99692215 | T | C | 3 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0028g0128 |
3 | HG00738.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.843+697T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692215 | |||||||
| chr10:99692220 | A | C | 140 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(137): Show |
188 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.843+702A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692220 | |||||||
| chr10:99692455 | C | T | 265 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(262): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.843+937C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692455 | |||||||
| chr10:99692460 | A | G | 2 | a0001c0001t0005g0282 a0004c0010t0005g0286 |
2 | HG01074.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.843+942A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692460 | |||||||
| chr10:99692485 | T | C | 1 | a0001c0001t0005g0287 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.843+967T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692485 | |||||||
| chr10:99692530 | C | CT | 122 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(119): Show |
143 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.843+1024dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 99692530 | ||||||
| chr10:99692530 | C | CTT | 129 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(126): Show |
171 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.843+1023_843+1024d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 99692530 | ||||||
| chr10:99692530 | C | CTTT | 10 | a0001c0001t0002g0175 a0001c0001t0002g0184 a0002c0002t0001g0154 others(7): Show |
16 | HG01243.hp1 HG01358.hp1 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.843+1022_843+1024d others(5): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 99692530 | ||||||
| chr10:99692579 | G | A | 1 | a0001c0001t0003g0210 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.843+1061G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692579 | |||||||
| chr10:99692612 | G | A | 4 | a0001c0001t0012g0015 a0001c0001t0012g0096 a0001c0001t0041g0095 others(1): Show |
6 | HG02451.hp1 HG02630.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+1094G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692612 | |||||||
| chr10:99692685 | T | G | 3 | a0001c0001t0002g0047 a0001c0001t0002g0049 a0001c0001t0002g0050 |
3 | HG02896.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.843+1167T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692685 | |||||||
| chr10:99692703 | A | C | 3 | a0001c0001t0010g0106 a0001c0001t0017g0025 a0001c0001t0032g0166 |
4 | HG02451.hp2 HG02615.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+1185A>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692703 | |||||||
| chr10:99692737 | C | T | 76 | a0001c0003t0001g0101 a0001c0003t0001g0158 a0001c0003t0001g0159 others(73): Show |
101 | HG00438.hp1 HG00558.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.843+1219C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692737 | |||||||
| chr10:99692870 | GTGA | G | 120 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(117): Show |
141 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.843+1358_843+1360d others(5): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 99692870 | ||||||
| chr10:99692954 | C | T | 2 | a0001c0001t0004g0023 a0001c0001t0043g0080 |
3 | HG00280.hp2 HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.843+1436C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692954 | |||||||
| chr10:99692997 | G | A | 1 | a0001c0001t0041g0095 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.843+1479G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99692997 | |||||||
| chr10:99693202 | C | G | 1 | a0001c0001t0005g0287 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.843+1684C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99693202 | |||||||
| chr10:99693309 | C | T | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.843+1791C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99693309 | |||||||
| chr10:99693504 | C | T | 262 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(259): Show |
332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.843+1986C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99693504 | |||||||
| chr10:99693614 | C | T | 1 | a0001c0001t0010g0026 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.843+2096C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99693614 | |||||||
| chr10:99693646 | G | A | 5 | a0001c0001t0005g0284 a0001c0001t0005g0292 a0001c0001t0005g0301 others(2): Show |
5 | HG01081.hp2 HG02717.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.843+2128G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99693646 | |||||||
| chr10:99693805 | C | A | 5 | a0001c0001t0003g0019 a0001c0001t0003g0221 a0001c0001t0003g0250 others(2): Show |
7 | HG01109.hp2 HG02559.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.844-2151C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99693805 | |||||||
| chr10:99693938 | C | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.844-2018C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99693938 | |||||||
| chr10:99694080 | G | A | 120 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(117): Show |
141 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.844-1876G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99694080 | |||||||
| chr10:99694385 | A | G | 262 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(259): Show |
332 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.844-1571A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99694385 | |||||||
| chr10:99694534 | T | A | 1 | a0002c0002t0001g0129 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.844-1422T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99694534 | |||||||
| chr10:99694538 | G | GT | 245 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(242): Show |
314 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.844-1403dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 99694538 | ||||||
| chr10:99694538 | G | GTT | 17 | a0001c0001t0002g0184 a0001c0001t0002g0186 a0001c0001t0002g0188 others(14): Show |
18 | HG01884.hp1 HG01928.hp1 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.844-1404_844-1403d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 99694538 | ||||||
| chr10:99694606 | G | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.844-1350G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99694606 | |||||||
| chr10:99694830 | C | G | 4 | a0001c0001t0005g0042 a0001c0001t0005g0248 a0001c0001t0005g0268 others(1): Show |
5 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-1126C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99694830 | |||||||
| chr10:99694953 | T | C | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.844-1003T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99694953 | |||||||
| chr10:99694955 | T | C | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.844-1001T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99694955 | |||||||
| chr10:99694978 | A | G | 3 | a0001c0001t0003g0259 a0001c0001t0003g0266 a0001c0001t0003g0267 |
3 | HG01167.hp1 HG01169.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.844-978A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99694978 | |||||||
| chr10:99695042 | T | C | 3 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0160 |
3 | HG01884.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.844-914T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99695042 | |||||||
| chr10:99695157 | G | A | 2 | a0001c0001t0012g0096 a0001c0003t0029g0107 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.844-799G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99695157 | |||||||
| chr10:99695608 | A | AT | 119 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(116): Show |
140 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.844-347dupT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr10 | 99695608 | ||||||
| chr10:99695610 | G | T | 315 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(312): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.844-346G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99695610 | |||||||
| chr10:99695751 | C | T | 269 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(266): Show |
345 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.844-205C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 8/12 | chr10 | 99695751 | |||||||
| chr10:99696262 | C | T | 1 | a0001c0001t0003g0306 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1010+140C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99696262 | |||||||
| chr10:99696697 | T | C | 5 | a0002c0002t0001g0131 a0002c0002t0001g0135 a0002c0002t0001g0136 others(2): Show |
5 | HG00558.hp1 HG00673.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1010+575T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99696697 | |||||||
| chr10:99696830 | A | G | 1 | a0001c0001t0002g0200 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1010+708A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99696830 | |||||||
| chr10:99696961 | ATGAAAGG others(7): Show |
A | 1 | a0002c0002t0001g0143 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1010+843_1010+856d others(16): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 99696961 | ||||||
| chr10:99696983 | A | G | 1 | a0001c0001t0010g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1010+861A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99696983 | |||||||
| chr10:99697398 | A | G | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1011-1136A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99697398 | |||||||
| chr10:99697409 | T | C | 3 | a0001c0001t0004g0024 a0001c0001t0004g0087 a0001c0001t0004g0089 |
4 | HG00673.hp1 NA18959.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1011-1125T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99697409 | |||||||
| chr10:99697438 | G | C | 1 | a0001c0001t0005g0044 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1011-1096G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99697438 | |||||||
| chr10:99697460 | C | A | 1 | a0001c0001t0002g0016 | 3 | HG00140.hp1 HG00642.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1011-1074C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99697460 | |||||||
| chr10:99697620 | A | T | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1011-914A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99697620 | |||||||
| chr10:99697750 | A | G | 1 | a0001c0001t0005g0275 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1011-784A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99697750 | |||||||
| chr10:99698047 | A | G | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1011-487A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99698047 | |||||||
| chr10:99698100 | A | G | 1 | a0002c0002t0001g0155 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1011-434A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99698100 | |||||||
| chr10:99698196 | C | T | 43 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0014 others(40): Show |
56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.1011-338C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99698196 | |||||||
| chr10:99698333 | C | T | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1011-201C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | chr10 | 99698333 | |||||||
| chr10:99698497 | G | GTGTT | 14 | a0001c0001t0003g0018 a0001c0001t0003g0020 a0001c0001t0003g0198 others(11): Show |
17 | HG00733.hp2 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1011-19_1011-16dup others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr10 | 99698497 | ||||||
| chr10:99699158 | T | A | 2 | a0001c0001t0009g0082 a0001c0001t0009g0083 |
2 | HG01255.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1335+300T>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99699158 | |||||||
| chr10:99699283 | G | T | 265 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(262): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1335+425G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99699283 | |||||||
| chr10:99699346 | A | G | 1 | a0001c0001t0009g0084 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1335+488A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99699346 | |||||||
| chr10:99699545 | C | T | 1 | a0002c0002t0001g0114 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1335+687C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99699545 | |||||||
| chr10:99699566 | A | T | 1 | a0001c0001t0003g0250 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1335+708A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99699566 | |||||||
| chr10:99699588 | G | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1335+730G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99699588 | |||||||
| chr10:99699658 | G | A | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1335+800G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99699658 | |||||||
| chr10:99699797 | C | T | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1335+939C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99699797 | |||||||
| chr10:99699855 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02818.hp1 HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1335+997C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99699855 | |||||||
| chr10:99699864 | C | G | 3 | a0001c0005t0008g0005 a0003c0004t0008g0005 a0003c0004t0008g0168 |
7 | HG02109.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1335+1006C>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99699864 | |||||||
| chr10:99700090 | G | A | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1336-883G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99700090 | |||||||
| chr10:99700096 | T | C | 1 | a0001c0001t0002g0188 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1336-877T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99700096 | |||||||
| chr10:99700393 | CGTGTGTG others(15): Show |
C | 1 | a0002c0002t0001g0125 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1336-559_1336-538d others(24): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700393 | ||||||
| chr10:99700394 | GTGTGTGT others(13): Show |
G | 124 | a0001c0001t0003g0012 a0001c0001t0003g0017 a0001c0001t0003g0018 others(121): Show |
163 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.1336-559_1336-540d others(22): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700394 | ||||||
| chr10:99700396 | GTGTGTGT others(11): Show |
G | 50 | a0001c0001t0002g0001 a0001c0001t0002g0190 a0001c0001t0002g0197 others(47): Show |
58 | HG00280.hp1 HG00673.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1336-559_1336-542d others(20): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700396 | ||||||
| chr10:99700398 | GTGTGTGT others(9): Show |
G | 13 | a0001c0001t0002g0194 a0001c0001t0005g0043 a0001c0001t0005g0284 others(10): Show |
13 | HG01081.hp2 HG02015.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.1336-559_1336-544d others(18): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700398 | ||||||
| chr10:99700400 | GTGTGTGT others(7): Show |
G | 50 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(47): Show |
67 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1336-559_1336-546d others(16): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700400 | ||||||
| chr10:99700402 | GTGTGTGT others(5): Show |
G | 3 | a0001c0001t0002g0196 a0001c0001t0010g0106 a0001c0001t0016g0033 |
3 | HG01516.hp2 HG02451.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1336-559_1336-548d others(14): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700402 | ||||||
| chr10:99700404 | GTGTGTGT others(3): Show |
G | 4 | a0001c0001t0001g0094 a0001c0001t0002g0181 a0001c0001t0002g0185 others(1): Show |
4 | HG00639.hp2 HG02818.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-559_1336-550d others(12): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700404 | ||||||
| chr10:99700406 | GTGTGTGT others(1): Show |
G | 5 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0017g0025 others(2): Show |
6 | HG02615.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1336-559_1336-552d others(10): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700406 | ||||||
| chr10:99700410 | GTGTA | G | 3 | a0001c0001t0005g0289 a0001c0001t0012g0015 a0001c0001t0012g0096 |
5 | HG02630.hp1 HG02698.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-559_1336-556d others(6): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700410 | ||||||
| chr10:99700412 | GTA | G | 4 | a0001c0001t0042g0097 a0001c0005t0008g0005 a0003c0004t0008g0005 others(1): Show |
6 | HG02109.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1336-559_1336-558d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700412 | ||||||
| chr10:99700414 | A | ATG | 3 | a0001c0001t0004g0014 a0001c0001t0004g0089 a0001c0001t0009g0055 |
3 | HG02683.hp1 HG02970.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1336-529_1336-528d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700414 | ||||||
| chr10:99700414 | A | G | 17 | a0001c0001t0001g0092 a0001c0001t0002g0001 a0001c0001t0002g0039 others(14): Show |
19 | HG00738.hp1 HG01993.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.1336-559A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99700414 | |||||||
| chr10:99700414 | ATG | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0014 a0001c0001t0004g0021 others(1): Show |
4 | HG00140.hp2 HG00733.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1336-529_1336-528d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700414 | ||||||
| chr10:99700426 | GTGTGTGT others(12): Show |
G | 8 | a0001c0001t0003g0211 a0001c0001t0003g0235 a0001c0001t0003g0273 others(5): Show |
8 | HG00738.hp1 HG01993.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1336-545_1336-527d others(21): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700426 | ||||||
| chr10:99700430 | GTGTGTGT others(8): Show |
G | 4 | a0001c0001t0002g0001 a0001c0001t0002g0039 a0001c0001t0002g0183 others(1): Show |
4 | NA18953.hp2 NA18970.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-541_1336-527d others(17): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700430 | ||||||
| chr10:99700432 | GTGTGTGT others(6): Show |
G | 1 | a0001c0001t0002g0001 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1336-539_1336-527d others(15): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr10 | 99700432 | ||||||
| chr10:99700446 | T | G | 3 | a0001c0001t0015g0037 a0002c0002t0001g0126 a0002c0002t0001g0156 |
4 | HG01099.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-527T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99700446 | |||||||
| chr10:99700447 | T | G | 1 | a0002c0002t0001g0165 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1336-526T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99700447 | |||||||
| chr10:99700448 | A | G | 1 | a0001c0001t0041g0095 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1336-525A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99700448 | |||||||
| chr10:99700606 | G | A | 1 | a0002c0002t0013g0137 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1336-367G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99700606 | |||||||
| chr10:99700708 | G | A | 1 | a0001c0001t0003g0311 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1336-265G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99700708 | |||||||
| chr10:99700776 | G | A | 1 | a0001c0001t0003g0230 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1336-197G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99700776 | |||||||
| chr10:99700917 | A | G | 1 | a0002c0002t0001g0136 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1336-56A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 10/12 | chr10 | 99700917 | |||||||
| chr10:99701225 | C | T | 1 | a0001c0001t0004g0068 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1421+167C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99701225 | |||||||
| chr10:99701266 | A | T | 269 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(266): Show |
345 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1421+208A>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99701266 | |||||||
| chr10:99701289 | G | T | 1 | a0001c0001t0003g0227 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1421+231G>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99701289 | |||||||
| chr10:99701290 | AT | A | 120 | a0001c0001t0002g0194 a0001c0001t0002g0199 a0001c0001t0003g0012 others(117): Show |
141 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.1421+247delT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 99701290 | ||||||
| chr10:99701290 | ATT | A | 140 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(137): Show |
188 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.1421+246_1421+247d others(4): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 99701290 | ||||||
| chr10:99701371 | T | C | 1 | a0001c0003t0029g0107 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1421+313T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99701371 | |||||||
| chr10:99701391 | G | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1421+333G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99701391 | |||||||
| chr10:99701433 | A | G | 2 | a0001c0001t0002g0049 a0001c0001t0002g0050 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1421+375A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99701433 | |||||||
| chr10:99701594 | G | A | 1 | a0001c0001t0004g0066 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1421+536G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99701594 | |||||||
| chr10:99701777 | G | A | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1421+719G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99701777 | |||||||
| chr10:99702006 | G | A | 1 | a0002c0002t0001g0169 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1422-506G>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99702006 | |||||||
| chr10:99702011 | T | TGCACTCC others(1): Show |
3 | a0001c0001t0009g0082 a0001c0001t0009g0083 a0001c0001t0009g0084 |
3 | HG01192.hp1 HG01255.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1422-498_1422-491d others(10): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 99702011 | ||||||
| chr10:99702054 | AAAACAAA others(14): Show |
A | 2 | a0001c0001t0035g0296 a0001c0001t0036g0300 |
2 | HG01433.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1422-449_1422-429d others(23): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr10 | 99702054 | ||||||
| chr10:99702131 | A | G | 1 | a0001c0001t0005g0289 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1422-381A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99702131 | |||||||
| chr10:99702235 | C | A | 265 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(262): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1422-277C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99702235 | |||||||
| chr10:99702277 | T | C | 1 | a0001c0001t0040g0167 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1422-235T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99702277 | |||||||
| chr10:99702436 | C | T | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1422-76C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99702436 | |||||||
| chr10:99702456 | G | C | 5 | a0001c0001t0005g0284 a0001c0001t0005g0292 a0001c0001t0005g0301 others(2): Show |
5 | HG01081.hp2 HG02717.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1422-56G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99702456 | |||||||
| chr10:99702491 | T | C | 1 | a0001c0001t0032g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1422-21T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 11/12 | chr10 | 99702491 | |||||||
| chr10:99702685 | C | T | 2 | a0001c0001t0005g0279 a0001c0001t0005g0280 |
2 | NA18985.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1583+12C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99702685 | |||||||
| chr10:99702848 | C | T | 1 | a0001c0001t0004g0059 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1583+175C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99702848 | |||||||
| chr10:99702990 | T | G | 1 | a0001c0001t0017g0025 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1583+317T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99702990 | |||||||
| chr10:99703025 | A | G | 260 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(257): Show |
329 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.1583+352A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99703025 | |||||||
| chr10:99703159 | T | C | 1 | a0001c0001t0015g0037 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1583+486T>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99703159 | |||||||
| chr10:99703248 | C | CA | 5 | a0002c0002t0001g0131 a0002c0002t0001g0135 a0002c0002t0001g0136 others(2): Show |
5 | HG00558.hp1 HG00673.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1583+575_1583+576i others(3): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99703248 | |||||||
| chr10:99703248 | C | CT | 264 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(261): Show |
340 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1583+575_1583+576i others(3): Show |
ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99703248 | |||||||
| chr10:99703323 | C | T | 1 | a0001c0003t0029g0107 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1583+650C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99703323 | |||||||
| chr10:99703424 | A | G | 265 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0172 others(262): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1583+751A>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99703424 | |||||||
| chr10:99703539 | T | G | 1 | a0001c0001t0032g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1583+866T>G | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99703539 | |||||||
| chr10:99703672 | CT | C | 4 | a0001c0001t0014g0285 a0001c0001t0014g0295 a0001c0001t0014g0297 others(1): Show |
4 | HG02523.hp2 HG03834.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1584-777delT | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr10 | 99703672 | ||||||
| chr10:99703928 | G | C | 4 | a0001c0001t0012g0015 a0001c0001t0012g0096 a0001c0001t0041g0095 others(1): Show |
6 | HG02451.hp1 HG02630.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1584-524G>C | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99703928 | |||||||
| chr10:99703968 | C | A | 1 | a0001c0001t0003g0252 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1584-484C>A | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99703968 | |||||||
| chr10:99704372 | C | T | 1 | a0001c0001t0004g0061 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1584-80C>T | ENTPD7 | ENSG00000198018.7 | transcript | ENST00000370489.5 | protein_coding | 12/12 | chr10 | 99704372 |