Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25975 |
| ensemblid | ENSG00000198759.12 |
| hgncid | 3235 |
| symbol | EGFL6 |
| name | EGF like domain multiple 6 |
| refseq_nuc | NM_015507.4 |
| refseq_prot | NP_056322.2 |
| ensembl_nuc | ENST00000361306.6 |
| ensembl_prot | ENSP00000355126.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 13569601 |
| end | 13633575 |
| strand | + |
| ver | v1.2 |
| region | chrX:13569601-13633575 |
| region5000 | chrX:13564601-13638575 |
| regionname0 | EGFL6_chrX_13569601_13633575 |
| regionname5000 | EGFL6_chrX_13564601_13638575 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 553 | 237 | 42 | 43 | 108 | 11 | 31 | 86 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0002 | 0/0 | 553 | 45 | 17 | 3 | 24 | 0 | 1 | 21 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0003 | 0/0 | 553 | 5 | 0 | 3 | 2 | 0 | 0 | 2 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0004 | 0/0 | 553 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0005 | 0/0 | 553 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0006 | 0/0 | 553 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0007 | 0/0 | 553 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0008 | 0/0 | 553 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0009 | 0/0 | 553 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0010 | 0/0 | 553 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0011 | 0/0 | 553 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| a0012 | 0/0 | 553 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | MPLPW others(548): Show |
chrX | 13564601 | 13638575 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1659 | 207 | 29 | 37 | 102 | 11 | 26 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0001c0004 | 0/0 | 1659 | 12 | 2 | 3 | 5 | 0 | 2 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0001c0005 | 0/0 | 1659 | 9 | 8 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0001c0007 | 0/0 | 1659 | 4 | 1 | 0 | 1 | 0 | 2 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0001c0008 | 0/0 | 1659 | 3 | 2 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0001c0017 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0001c0018 | 0/0 | 1659 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0002c0002 | 0/0 | 1659 | 24 | 0 | 0 | 24 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0002c0003 | 0/0 | 1659 | 19 | 15 | 3 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0002c0024 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0002c0025 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0003c0006 | 0/0 | 1659 | 5 | 0 | 3 | 2 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0004c0010 | 0/0 | 1659 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0004c0020 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0004c0021 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0005c0012 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0005c0013 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0005c0014 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0006c0009 | 0/0 | 1659 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0007c0016 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0008c0015 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0009c0023 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0010c0011 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0011c0019 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 | ||
| a0012c0022 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | ATGCC others(1654): Show |
chrX | 13564601 | 13638575 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2403 | 105 | 12 | 28 | 48 | 4 | 11 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0001t0002 | 0/0 | 2403 | 57 | 8 | 3 | 41 | 2 | 3 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0001t0003 | 0/0 | 2403 | 33 | 4 | 4 | 10 | 5 | 10 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0001t0004 | 0/0 | 2403 | 4 | 2 | 2 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0001t0005 | 0/0 | 2403 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0001t0008 | 0/0 | 2403 | 4 | 1 | 0 | 2 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0001t0009 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0001t0010 | 0/0 | 2403 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0004t0001 | 0/0 | 2403 | 4 | 1 | 1 | 1 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0004t0002 | 0/0 | 2403 | 3 | 0 | 0 | 3 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0004t0003 | 0/0 | 2403 | 3 | 0 | 2 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0004t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0004t0008 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0005t0001 | 0/0 | 2403 | 8 | 7 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0005t0002 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0007t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0007t0003 | 0/0 | 2403 | 3 | 0 | 0 | 1 | 0 | 2 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0008t0001 | 0/0 | 2403 | 3 | 2 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0017t0003 | 0/0 | 2403 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0001c0018t0002 | 0/0 | 2403 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0002c0002t0004 | 0/0 | 2403 | 10 | 0 | 0 | 10 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0002c0002t0005 | 0/0 | 2403 | 4 | 0 | 0 | 4 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0002c0002t0006 | 0/0 | 2403 | 5 | 0 | 0 | 5 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0002c0002t0007 | 0/0 | 2403 | 5 | 0 | 0 | 5 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0002c0003t0004 | 0/0 | 2403 | 13 | 10 | 3 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0002c0003t0005 | 0/0 | 2403 | 4 | 3 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0002c0003t0006 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0002c0003t0007 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0002c0024t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0002c0025t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0003c0006t0002 | 0/0 | 2403 | 2 | 0 | 2 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0003c0006t0004 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0003c0006t0006 | 0/0 | 2403 | 2 | 0 | 1 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0004c0010t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0004c0010t0003 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0004c0020t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0004c0021t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0005c0012t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0005c0013t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0005c0014t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0006c0009t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0006c0009t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0007c0016t0004 | 0/0 | 2403 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0008c0015t0007 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0009c0023t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0010c0011t0004 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0011c0019t0001 | 0/0 | 2403 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| a0012c0022t0001 | 0/0 | 2403 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | GCTCA others(2398): Show |
chrX | 13564601 | 13638575 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0036 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0290 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0008g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0009g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0001t0010g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0003g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0004t0008g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0005t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0005t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0005t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0005t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0005t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0005t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0007t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0007t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0007t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0007t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0008t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0008t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0008t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0017t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0001c0018t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0005g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0006g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0007g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0007g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0002t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0003t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0024t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0002c0025t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0003c0006t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0003c0006t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0003c0006t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0003c0006t0006g0005 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0004c0010t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0004c0010t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0004c0020t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0004c0021t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0005c0012t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0005c0013t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0005c0014t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0006c0009t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0006c0009t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0007c0016t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0008c0015t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0009c0023t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0010c0011t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0011c0019t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| a0012c0022t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0233 | EUR | GBR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0103 | EUR | GBR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | GBR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0273 | EUR | FIN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0242 | EUR | FIN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00544 | hp1 | a0001 | c0004 | t0008 | g0015 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00621 | hp1 | a0002 | c0002 | t0006 | g0146 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0196 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01070 | hp1 | a0002 | c0003 | t0004 | g0158 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0223 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0247 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01074 | hp1 | a0002 | c0003 | t0004 | g0159 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01106 | hp1 | a0001 | c0005 | t0001 | g0057 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01109 | hp1 | a0007 | c0016 | t0004 | g0026 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01167 | hp1 | a0001 | c0004 | t0003 | g0004 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01169 | hp2 | a0001 | c0004 | t0003 | g0004 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01243 | hp1 | a0002 | c0003 | t0004 | g0002 | AMR | PUR | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01346 | hp2 | a0001 | c0017 | t0003 | g0078 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0093 | EUR | IBS | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01891 | hp1 | a0002 | c0003 | t0004 | g0169 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01975 | hp1 | a0003 | c0006 | t0002 | g0138 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02004 | hp1 | a0003 | c0006 | t0002 | g0129 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02027 | hp1 | a0001 | c0007 | t0003 | g0101 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02132 | hp1 | a0001 | c0001 | t0009 | g0214 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0220 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02148 | hp2 | a0003 | c0006 | t0006 | g0005 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | CDX | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02155 | hp2 | a0002 | c0002 | t0007 | g0022 | EAS | CDX | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02258 | hp1 | a0005 | c0014 | t0001 | g0028 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02280 | hp2 | a0008 | c0015 | t0007 | g0010 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02293 | hp1 | a0001 | c0008 | t0001 | g0056 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02451 | hp1 | a0002 | c0003 | t0005 | g0053 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02451 | hp2 | a0001 | c0004 | t0001 | g0069 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02523 | hp2 | a0002 | c0002 | t0006 | g0156 | EAS | KHV | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02572 | hp1 | a0001 | c0004 | t0004 | g0059 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02615 | hp2 | a0002 | c0003 | t0004 | g0164 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02622 | hp1 | a0001 | c0005 | t0001 | g0055 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02630 | hp1 | a0006 | c0009 | t0004 | g0034 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02630 | hp2 | a0010 | c0011 | t0004 | g0058 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02647 | hp1 | a0004 | c0021 | t0001 | g0042 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0295 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02723 | hp2 | a0001 | c0007 | t0001 | g0274 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02809 | hp2 | a0011 | c0019 | t0001 | g0226 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0280 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02895 | hp1 | a0001 | c0008 | t0001 | g0040 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02965 | hp1 | a0002 | c0003 | t0005 | g0048 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02970 | hp1 | a0002 | c0024 | t0004 | g0266 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02976 | hp1 | a0005 | c0012 | t0001 | g0054 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03017 | hp1 | a0001 | c0004 | t0001 | g0238 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03041 | hp1 | a0001 | c0005 | t0002 | g0127 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03041 | hp2 | a0004 | c0010 | t0001 | g0236 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03139 | hp1 | a0004 | c0010 | t0003 | g0090 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03195 | hp2 | a0001 | c0008 | t0001 | g0296 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03209 | hp1 | a0002 | c0003 | t0004 | g0031 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03239 | hp2 | a0001 | c0004 | t0003 | g0064 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03453 | hp1 | a0002 | c0003 | t0004 | g0234 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03453 | hp2 | a0002 | c0003 | t0004 | g0002 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03486 | hp1 | a0002 | c0025 | t0004 | g0030 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0012 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03491 | hp2 | a0001 | c0007 | t0003 | g0177 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03492 | hp1 | a0001 | c0007 | t0003 | g0178 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03516 | hp2 | a0002 | c0003 | t0004 | g0284 | AFR | ESN | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03540 | hp1 | a0002 | c0003 | t0004 | g0033 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03579 | hp1 | a0001 | c0005 | t0001 | g0244 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03654 | hp1 | a0002 | c0003 | t0005 | g0081 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03688 | hp1 | a0001 | c0018 | t0002 | g0067 | SAS | STU | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0130 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03834 | hp2 | a0001 | c0001 | t0010 | g0097 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0085 | SAS | STU | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | BEB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0294 | SAS | STU | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18522 | hp1 | a0002 | c0003 | t0005 | g0052 | AFR | YRI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0225 | AFR | YRI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18939 | hp1 | a0002 | c0002 | t0006 | g0135 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18939 | hp2 | a0002 | c0002 | t0004 | g0021 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18941 | hp1 | a0002 | c0002 | t0004 | g0207 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18943 | hp1 | a0002 | c0002 | t0005 | g0020 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18944 | hp1 | a0002 | c0002 | t0006 | g0106 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18946 | hp2 | a0002 | c0002 | t0007 | g0001 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18954 | hp2 | a0002 | c0002 | t0007 | g0001 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18956 | hp2 | a0002 | c0002 | t0004 | g0215 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18959 | hp1 | a0003 | c0006 | t0004 | g0291 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18964 | hp2 | a0002 | c0002 | t0005 | g0166 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18968 | hp1 | a0002 | c0002 | t0004 | g0265 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18974 | hp1 | a0002 | c0002 | t0004 | g0282 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18977 | hp1 | a0002 | c0002 | t0004 | g0009 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18979 | hp2 | a0002 | c0002 | t0007 | g0019 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18983 | hp1 | a0001 | c0001 | t0008 | g0013 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18990 | hp1 | a0002 | c0002 | t0005 | g0167 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18993 | hp2 | a0003 | c0006 | t0006 | g0005 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18994 | hp1 | a0012 | c0022 | t0001 | g0038 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19002 | hp2 | a0002 | c0002 | t0007 | g0018 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19004 | hp1 | a0002 | c0002 | t0004 | g0264 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | LWK | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | LWK | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19043 | hp1 | a0002 | c0003 | t0004 | g0037 | AFR | LWK | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19056 | hp1 | a0001 | c0004 | t0001 | g0016 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19057 | hp1 | a0001 | c0004 | t0002 | g0134 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19057 | hp2 | a0002 | c0002 | t0004 | g0095 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19064 | hp2 | a0002 | c0002 | t0004 | g0017 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19065 | hp1 | a0002 | c0002 | t0004 | g0213 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19066 | hp1 | a0002 | c0002 | t0005 | g0080 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19072 | hp1 | a0001 | c0004 | t0002 | g0132 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19074 | hp2 | a0002 | c0002 | t0006 | g0104 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19084 | hp1 | a0001 | c0004 | t0002 | g0133 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | YRI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | YRI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ASW | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA20129 | hp2 | a0002 | c0003 | t0004 | g0032 | AFR | ASW | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0089 | EUR | TSI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0173 | EUR | TSI | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0088 | SAS | GIH | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02109 | hp1 | a0002 | c0003 | t0004 | g0285 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02486 | hp1 | a0004 | c0020 | t0001 | g0047 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02559 | hp1 | a0001 | c0005 | t0001 | g0160 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG02559 | hp2 | a0009 | c0023 | t0001 | g0046 | AFR | ACB | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG03471 | hp1 | a0002 | c0003 | t0007 | g0011 | AFR | MSL | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG06807 | hp1 | a0001 | c0005 | t0001 | g0272 | AFR | USA | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| HG06807 | hp2 | a0002 | c0003 | t0006 | g0043 | AFR | USA | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA20300 | hp1 | a0006 | c0009 | t0001 | g0283 | AFR | USA | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA20300 | hp2 | a0005 | c0013 | t0004 | g0029 | AFR | USA | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | LWK | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | LWK | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0290 | REF | REF | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0036 | REF | REF | EGFL6_chrX_13564601_13638575 | EGFL6 | chrX | 13564601 | 13638575 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:13594844 | G | A | 4 | a0005 a0006 a0008 others(1): Show |
7 | HG02258.hp1 HG02280.hp2 HG02630.hp1 others(4): Show |
missense_variant | MODERATE | c.196G>A | p.Glu66Lys | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/12 | 457/2403 | 196/1662 | 66/553 | chrX | 13594844 | |||
| chrX:13600001 | C | T | 2 | a0006 a0008 |
3 | HG02280.hp2 HG02630.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.307C>T | p.Arg103Trp | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/12 | 568/2403 | 307/1662 | 103/553 | chrX | 13600001 | |||
| chrX:13603406 | C | T | 1 | a0009 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.490C>T | p.Arg164Cys | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/12 | 751/2403 | 490/1662 | 164/553 | chrX | 13603406 | |||
| chrX:13606379 | A | G | 1 | a0012 | 1 | NA18994.hp1 | missense_variant&splice_region_variant | MODERATE | c.521A>G | p.Asp174Gly | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/12 | 782/2403 | 521/1662 | 174/553 | chrX | 13606379 | |||
| chrX:13606511 | T | A | 1 | a0007 | 1 | HG01109.hp1 | missense_variant&splice_region_variant | MODERATE | c.653T>A | p.Ile218Lys | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/12 | 914/2403 | 653/1662 | 218/553 | chrX | 13606511 | |||
| chrX:13619187 | A | G | 1 | a0003 | 5 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
missense_variant | MODERATE | c.1127A>G | p.Glu376Gly | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/12 | 1388/2403 | 1127/1662 | 376/553 | chrX | 13619187 | |||
| chrX:13627249 | G | T | 2 | a0004 a0009 |
5 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(2): Show |
missense_variant | MODERATE | c.1524G>T | p.Leu508Phe | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/12 | 1785/2403 | 1524/1662 | 508/553 | chrX | 13627249 | |||
| chrX:13633006 | G | A | 1 | a0011 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.1573G>A | p.Gly525Ser | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 1834/2403 | 1573/1662 | 525/553 | chrX | 13633006 | |||
| chrX:13633036 | G | A | 3 | a0002 a0007 a0008 |
47 | HG00621.hp1 HG01070.hp1 HG01074.hp1 others(44): Show |
missense_variant | MODERATE | c.1603G>A | p.Asp535Asn | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 1864/2403 | 1603/1662 | 535/553 | chrX | 13633036 | |||
| chrX:13633042 | G | A | 1 | a0010 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1609G>A | p.Val537Ile | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 1870/2403 | 1609/1662 | 537/553 | chrX | 13633042 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:13600018 | A | G | 5 | a0001c0005 a0002c0025 a0005c0014 others(2): Show |
14 | HG01106.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
synonymous_variant | LOW | c.324A>G | p.Arg108Arg | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/12 | 585/2403 | 324/1662 | 108/553 | chrX | 13600018 | |||
| chrX:13600042 | C | T | 3 | a0001c0008 a0002c0024 a0005c0013 |
5 | HG02293.hp1 HG02895.hp1 HG02970.hp1 others(2): Show |
synonymous_variant | LOW | c.348C>T | p.Tyr116Tyr | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/12 | 609/2403 | 348/1662 | 116/553 | chrX | 13600042 | |||
| chrX:13600045 | G | A | 5 | a0001c0005 a0002c0025 a0005c0014 others(2): Show |
14 | HG01106.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
synonymous_variant | LOW | c.351G>A | p.Lys117Lys | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/12 | 612/2403 | 351/1662 | 117/553 | chrX | 13600045 | |||
| chrX:13606476 | C | T | 2 | a0001c0007 a0004c0021 |
5 | HG02027.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
synonymous_variant | LOW | c.618C>T | p.Phe206Phe | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/12 | 879/2403 | 618/1662 | 206/553 | chrX | 13606476 | |||
| chrX:13617818 | C | T | 3 | a0001c0004 a0002c0002 a0004c0010 |
38 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(35): Show |
synonymous_variant | LOW | c.867C>T | p.Ser289Ser | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/12 | 1128/2403 | 867/1662 | 289/553 | chrX | 13617818 | |||
| chrX:13618038 | C | A | 1 | a0001c0017 | 1 | HG01346.hp2 | synonymous_variant | LOW | c.1087C>A | p.Arg363Arg | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/12 | 1348/2403 | 1087/1662 | 363/553 | chrX | 13618038 | |||
| chrX:13627072 | G | A | 1 | a0001c0018 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.1347G>A | p.Leu449Leu | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/12 | 1608/2403 | 1347/1662 | 449/553 | chrX | 13627072 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:13569646 | T | A | 8 | a0001c0001t0003 a0001c0001t0005 a0001c0004t0003 others(5): Show |
51 | HG00099.hp2 HG00280.hp1 HG00735.hp1 others(48): Show |
5_prime_UTR_variant | MODIFIER | c.-216T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/12 | 216 | chrX | 13569646 | ||||||
| chrX:13569710 | T | G | 8 | a0001c0001t0002 a0001c0004t0002 a0001c0005t0002 others(5): Show |
72 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(69): Show |
5_prime_UTR_variant | MODIFIER | c.-152T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/12 | 152 | chrX | 13569710 | ||||||
| chrX:13569733 | C | G | 5 | a0001c0001t0008 a0001c0004t0008 a0002c0002t0007 others(2): Show |
12 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-129C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/12 | 129 | chrX | 13569733 | ||||||
| chrX:13633238 | G | A | 20 | a0001c0001t0004 a0001c0001t0005 a0001c0004t0004 others(17): Show |
60 | HG00621.hp1 HG01070.hp1 HG01070.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 143 | chrX | 13633238 | ||||||
| chrX:13633417 | A | G | 1 | a0001c0001t0002 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*322A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 322 | chrX | 13633417 | ||||||
| chrX:13633507 | C | T | 1 | a0001c0001t0010 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*412C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 412 | chrX | 13633507 | ||||||
| chrX:13633572 | A | G | 1 | a0001c0001t0009 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*477A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 12/12 | 477 | chrX | 13633572 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:13570095 | C | T | 1 | a0001c0008t0001g0296 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.74+160C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570095 | |||||||
| chrX:13570123 | T | C | 1 | a0001c0001t0001g0007 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.74+188T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570123 | |||||||
| chrX:13570158 | C | T | 1 | a0001c0001t0008g0295 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.74+223C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570158 | |||||||
| chrX:13570173 | A | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0181 others(112): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.74+238A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570173 | |||||||
| chrX:13570482 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0008g0012 a0001c0001t0008g0013 others(14): Show |
18 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.74+547G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570482 | |||||||
| chrX:13570563 | C | G | 1 | a0001c0008t0001g0296 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.74+628C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570563 | |||||||
| chrX:13570642 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.74+707A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570642 | |||||||
| chrX:13570739 | C | T | 1 | a0001c0001t0003g0179 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.74+804C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570739 | |||||||
| chrX:13570749 | T | C | 1 | a0001c0001t0003g0023 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.74+814T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13570749 | |||||||
| chrX:13571107 | C | CCCCCCA | 149 | a0001c0001t0001g0008 a0001c0001t0001g0060 a0001c0001t0001g0062 others(146): Show |
153 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.74+1175_74+1180dup others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13571107 | ||||||
| chrX:13571116 | A | C | 15 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0003g0049 others(12): Show |
16 | HG01243.hp1 HG02293.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.74+1181A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13571116 | |||||||
| chrX:13571522 | A | G | 3 | a0001c0001t0001g0041 a0001c0008t0001g0040 a0004c0021t0001g0042 |
3 | HG02647.hp1 HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.74+1587A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13571522 | |||||||
| chrX:13571643 | A | T | 152 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0060 others(149): Show |
156 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.74+1708A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13571643 | |||||||
| chrX:13571669 | G | A | 2 | a0001c0001t0001g0060 a0001c0004t0004g0059 |
2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.74+1734G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13571669 | |||||||
| chrX:13571844 | T | C | 161 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0041 others(158): Show |
165 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.74+1909T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13571844 | |||||||
| chrX:13572386 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.74+2451T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572386 | |||||||
| chrX:13572570 | G | A | 2 | a0001c0001t0002g0044 a0002c0003t0006g0043 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.74+2635G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572570 | |||||||
| chrX:13572639 | C | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0181 a0001c0001t0001g0182 others(36): Show |
40 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.74+2704C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572639 | |||||||
| chrX:13572760 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+2825G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572760 | |||||||
| chrX:13572837 | G | C | 15 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0003g0049 others(12): Show |
15 | HG01106.hp1 HG02293.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.74+2902G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572837 | |||||||
| chrX:13572868 | C | T | 9 | a0001c0001t0003g0049 a0001c0001t0005g0050 a0001c0001t0005g0051 others(6): Show |
9 | HG02293.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+2933C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572868 | |||||||
| chrX:13572960 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+3025T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13572960 | |||||||
| chrX:13573053 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG02735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.74+3118T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573053 | |||||||
| chrX:13573056 | C | T | 3 | a0001c0005t0001g0055 a0001c0008t0001g0056 a0005c0012t0001g0054 |
3 | HG02293.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.74+3121C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573056 | |||||||
| chrX:13573216 | C | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0289 |
3 | HG00597.hp2 HG02523.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.74+3281C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573216 | |||||||
| chrX:13573507 | T | G | 17 | a0001c0001t0001g0008 a0001c0001t0008g0012 a0001c0001t0008g0013 others(14): Show |
18 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.74+3572T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573507 | |||||||
| chrX:13573510 | T | C | 1 | a0001c0004t0003g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.74+3575T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573510 | |||||||
| chrX:13573546 | C | T | 3 | a0001c0005t0001g0055 a0001c0008t0001g0056 a0005c0012t0001g0054 |
3 | HG02293.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.74+3611C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573546 | |||||||
| chrX:13573656 | A | C | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+3721A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573656 | |||||||
| chrX:13573688 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0008g0012 a0001c0001t0008g0013 others(14): Show |
18 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.74+3753G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573688 | |||||||
| chrX:13573745 | G | T | 164 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0060 others(161): Show |
168 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.74+3810G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573745 | |||||||
| chrX:13573754 | TTTGATTT others(23): Show |
T | 12 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0003g0049 others(9): Show |
12 | HG02293.hp1 HG02451.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.74+3823_74+3852del others(30): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13573754 | ||||||
| chrX:13573815 | A | G | 2 | a0001c0007t0003g0177 a0001c0007t0003g0178 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.74+3880A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13573815 | |||||||
| chrX:13574011 | T | C | 5 | a0002c0003t0004g0031 a0002c0003t0004g0032 a0002c0003t0004g0033 others(2): Show |
5 | HG02630.hp1 HG03209.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+4076T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574011 | |||||||
| chrX:13574047 | G | A | 152 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0060 others(149): Show |
156 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.74+4112G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574047 | |||||||
| chrX:13574079 | C | T | 10 | a0001c0001t0002g0045 a0001c0001t0003g0049 a0001c0001t0005g0050 others(7): Show |
10 | HG02293.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.74+4144C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574079 | |||||||
| chrX:13574080 | G | A | 1 | a0001c0004t0003g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.74+4145G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574080 | |||||||
| chrX:13574327 | A | G | 1 | a0001c0005t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.74+4392A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574327 | |||||||
| chrX:13574397 | TGACAAAT others(5): Show |
T | 1 | a0002c0003t0006g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.74+4469_74+4480del others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13574397 | ||||||
| chrX:13574590 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.74+4655T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574590 | |||||||
| chrX:13574625 | G | A | 1 | a0001c0001t0003g0035 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.74+4690G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574625 | |||||||
| chrX:13574638 | G | A | 1 | a0001c0001t0001g0007 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.74+4703G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574638 | |||||||
| chrX:13574730 | C | CA | 20 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(17): Show |
21 | HG00597.hp2 HG01106.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.74+4810dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13574730 | ||||||
| chrX:13574730 | C | CAAA | 9 | a0001c0001t0003g0049 a0001c0001t0005g0050 a0001c0001t0005g0051 others(6): Show |
9 | HG02451.hp1 HG02622.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+4808_74+4810dup others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13574730 | ||||||
| chrX:13574762 | G | A | 165 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0060 others(162): Show |
169 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.74+4827G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574762 | |||||||
| chrX:13574801 | T | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0045 |
3 | HG02280.hp1 HG03831.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.74+4866T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574801 | |||||||
| chrX:13574806 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0002g0070 a0001c0004t0001g0069 |
3 | HG00639.hp1 HG02055.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.74+4871G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13574806 | |||||||
| chrX:13575004 | A | G | 4 | a0001c0008t0001g0296 a0002c0003t0004g0002 a0002c0003t0004g0037 others(1): Show |
5 | HG01243.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.74+5069A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575004 | |||||||
| chrX:13575094 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.74+5159C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575094 | |||||||
| chrX:13575111 | AAAAC | A | 11 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0218 others(8): Show |
11 | HG00673.hp1 HG01175.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+5210_74+5213del others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13575111 | ||||||
| chrX:13575111 | AAAACAAA others(1): Show |
A | 17 | a0001c0001t0001g0024 a0001c0001t0001g0072 a0001c0001t0002g0027 others(14): Show |
18 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.74+5206_74+5213del others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13575111 | ||||||
| chrX:13575111 | AAAACAAA others(5): Show |
A | 152 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0060 others(149): Show |
156 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.74+5202_74+5213del others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13575111 | ||||||
| chrX:13575111 | AAAACAAA others(9): Show |
A | 13 | a0001c0001t0002g0044 a0001c0001t0003g0049 a0001c0001t0005g0050 others(10): Show |
13 | HG02293.hp1 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.74+5198_74+5213del others(16): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13575111 | ||||||
| chrX:13575131 | C | A | 9 | a0001c0001t0003g0049 a0001c0001t0005g0050 a0001c0001t0005g0051 others(6): Show |
9 | HG02293.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+5196C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575131 | |||||||
| chrX:13575361 | C | T | 1 | a0001c0005t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.74+5426C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575361 | |||||||
| chrX:13575362 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.74+5427G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575362 | |||||||
| chrX:13575381 | G | A | 1 | a0002c0003t0005g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.74+5446G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575381 | |||||||
| chrX:13575442 | C | G | 17 | a0001c0001t0001g0008 a0001c0001t0008g0012 a0001c0001t0008g0013 others(14): Show |
18 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.74+5507C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575442 | |||||||
| chrX:13575713 | G | T | 1 | a0001c0005t0001g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.74+5778G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575713 | |||||||
| chrX:13575985 | G | A | 6 | a0001c0001t0003g0049 a0001c0001t0005g0050 a0001c0001t0005g0051 others(3): Show |
6 | HG02451.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.74+6050G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13575985 | |||||||
| chrX:13576076 | C | A | 152 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0060 others(149): Show |
156 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.74+6141C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576076 | |||||||
| chrX:13576252 | C | G | 1 | a0001c0001t0002g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.74+6317C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576252 | |||||||
| chrX:13576282 | A | G | 13 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0071 others(10): Show |
13 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.74+6347A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576282 | |||||||
| chrX:13576285 | C | A | 4 | a0001c0001t0001g0024 a0001c0001t0002g0027 a0001c0001t0004g0025 others(1): Show |
4 | HG01109.hp1 HG02257.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.74+6350C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576285 | |||||||
| chrX:13576308 | T | C | 172 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0041 others(169): Show |
177 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.74+6373T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576308 | |||||||
| chrX:13576477 | C | A | 11 | a0001c0001t0002g0044 a0001c0001t0003g0049 a0001c0001t0005g0050 others(8): Show |
11 | HG02293.hp1 HG02451.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+6542C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576477 | |||||||
| chrX:13576575 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.74+6640C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576575 | |||||||
| chrX:13576705 | G | C | 1 | a0001c0005t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.74+6770G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576705 | |||||||
| chrX:13576941 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+7006G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576941 | |||||||
| chrX:13576996 | A | T | 18 | a0001c0001t0001g0024 a0001c0001t0002g0027 a0001c0001t0004g0025 others(15): Show |
19 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+7061A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13576996 | |||||||
| chrX:13577118 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.74+7183T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577118 | |||||||
| chrX:13577296 | TTTTATAT others(3): Show |
T | 1 | a0005c0014t0001g0028 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.74+7363_74+7372del others(10): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | ||||||
| chrX:13577296 | TTTTATAT others(5): Show |
T | 1 | a0005c0013t0004g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.74+7363_74+7374del others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | ||||||
| chrX:13577296 | TTTTATAT others(7): Show |
T | 1 | a0006c0009t0004g0034 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.74+7363_74+7376del others(14): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | ||||||
| chrX:13577296 | TTTTATAT others(9): Show |
T | 3 | a0002c0003t0004g0002 a0002c0003t0006g0043 a0004c0020t0001g0047 |
3 | HG01243.hp1 HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.74+7363_74+7378del others(16): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | ||||||
| chrX:13577296 | TTTTATAT others(11): Show |
T | 5 | a0001c0001t0002g0044 a0001c0008t0001g0296 a0002c0003t0004g0002 others(2): Show |
5 | HG01891.hp1 HG02630.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.74+7363_74+7380del others(18): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | ||||||
| chrX:13577296 | TTTTATAT others(13): Show |
T | 4 | a0002c0003t0004g0031 a0002c0003t0004g0032 a0002c0003t0004g0033 others(1): Show |
4 | HG03209.hp1 HG03486.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+7363_74+7382del others(20): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | ||||||
| chrX:13577296 | TTTTATAT others(15): Show |
T | 6 | a0001c0001t0001g0024 a0001c0001t0002g0027 a0001c0001t0004g0025 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.74+7363_74+7384del others(22): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | ||||||
| chrX:13577296 | TTTTATAT others(21): Show |
T | 8 | a0001c0001t0001g0041 a0001c0004t0001g0016 a0001c0008t0001g0040 others(5): Show |
9 | HG02647.hp1 HG02895.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+7363_74+7390del others(28): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | ||||||
| chrX:13577296 | TTTTATAT others(23): Show |
T | 181 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0060 others(178): Show |
185 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.74+7363_74+7392del others(30): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577296 | ||||||
| chrX:13577297 | T | A | 2 | a0001c0001t0001g0185 a0001c0001t0002g0184 |
2 | NA18950.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.74+7362T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577297 | |||||||
| chrX:13577298 | T | A | 11 | a0001c0001t0001g0185 a0001c0001t0001g0224 a0001c0001t0002g0184 others(8): Show |
11 | HG01070.hp2 HG01106.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+7363T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577298 | |||||||
| chrX:13577298 | T | TTA | 17 | a0001c0001t0001g0007 a0001c0001t0001g0251 a0001c0001t0001g0252 others(14): Show |
17 | HG00673.hp1 HG01952.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.74+7406_74+7407dup others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | ||||||
| chrX:13577298 | T | TTATA | 10 | a0001c0001t0001g0219 a0001c0001t0001g0267 a0001c0001t0001g0268 others(7): Show |
10 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.74+7404_74+7407dup others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | ||||||
| chrX:13577298 | T | TTATATA | 4 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
4 | HG01261.hp1 HG01934.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+7402_74+7407dup others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | ||||||
| chrX:13577298 | TTA | T | 10 | a0001c0001t0001g0221 a0001c0001t0001g0237 a0001c0001t0003g0235 others(7): Show |
10 | HG00735.hp1 HG02109.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.74+7406_74+7407del others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | ||||||
| chrX:13577298 | TTATA | T | 14 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(11): Show |
14 | HG00099.hp1 HG00597.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.74+7404_74+7407del others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | ||||||
| chrX:13577298 | TTATATAT others(3): Show |
T | 1 | a0011c0019t0001g0226 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.74+7398_74+7407del others(10): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | ||||||
| chrX:13577298 | TTATATAT others(5): Show |
T | 1 | a0001c0005t0001g0225 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.74+7396_74+7407del others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577298 | ||||||
| chrX:13577315 | TATATATA others(25): Show |
T | 2 | a0001c0001t0001g0185 a0001c0001t0002g0184 |
2 | NA18950.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.74+7382_74+7413del others(32): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577315 | ||||||
| chrX:13577321 | TATATATA others(19): Show |
T | 7 | a0001c0001t0001g0224 a0001c0001t0003g0049 a0001c0001t0005g0050 others(4): Show |
7 | HG02451.hp1 HG02965.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.74+7388_74+7413del others(26): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577321 | ||||||
| chrX:13577323 | TATATATA others(17): Show |
T | 1 | a0001c0005t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.74+7390_74+7413del others(24): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577323 | ||||||
| chrX:13577325 | T | A | 8 | a0001c0001t0001g0041 a0001c0004t0001g0016 a0001c0008t0001g0040 others(5): Show |
9 | HG02647.hp1 HG02895.hp1 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+7390T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577325 | |||||||
| chrX:13577327 | T | A | 181 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0060 others(178): Show |
185 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.74+7392T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577327 | |||||||
| chrX:13577329 | TATATATA others(7): Show |
T | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+7398_74+7411del others(14): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577329 | ||||||
| chrX:13577340 | A | G | 4 | a0001c0001t0002g0125 a0001c0001t0002g0131 a0001c0001t0002g0137 others(1): Show |
4 | NA18954.hp1 NA18955.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+7405A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577340 | |||||||
| chrX:13577343 | C | T | 208 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(205): Show |
213 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.74+7408C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577343 | |||||||
| chrX:13577378 | C | G | 220 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(217): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.74+7443C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577378 | |||||||
| chrX:13577438 | T | C | 189 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(186): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.74+7503T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577438 | |||||||
| chrX:13577439 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.74+7504G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577439 | |||||||
| chrX:13577443 | A | G | 8 | a0001c0001t0001g0224 a0001c0001t0003g0049 a0001c0001t0005g0050 others(5): Show |
8 | HG01106.hp1 HG02451.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.74+7508A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577443 | |||||||
| chrX:13577475 | A | T | 1 | a0002c0002t0005g0166 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.74+7540A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577475 | |||||||
| chrX:13577603 | C | A | 199 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(196): Show |
204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.74+7668C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577603 | |||||||
| chrX:13577652 | G | C | 1 | a0001c0001t0001g0216 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.74+7717G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577652 | |||||||
| chrX:13577896 | G | C | 190 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(187): Show |
195 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.74+7961G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577896 | |||||||
| chrX:13577949 | A | C | 9 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(6): Show |
9 | HG01106.hp1 HG02451.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+8014A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13577949 | |||||||
| chrX:13577979 | T | TA | 18 | a0001c0001t0001g0024 a0001c0001t0002g0027 a0001c0001t0004g0025 others(15): Show |
19 | HG01109.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+8045dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13577979 | ||||||
| chrX:13578142 | C | T | 199 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(196): Show |
204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.74+8207C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578142 | |||||||
| chrX:13578256 | A | G | 1 | a0001c0005t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.74+8321A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578256 | |||||||
| chrX:13578260 | A | C | 218 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(215): Show |
224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.74+8325A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578260 | |||||||
| chrX:13578300 | G | C | 191 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(188): Show |
196 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.74+8365G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578300 | |||||||
| chrX:13578406 | A | T | 11 | a0001c0008t0001g0296 a0002c0003t0004g0002 a0002c0003t0004g0031 others(8): Show |
12 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.74+8471A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578406 | |||||||
| chrX:13578424 | A | G | 192 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(189): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.74+8489A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578424 | |||||||
| chrX:13578523 | G | C | 191 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(188): Show |
196 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.74+8588G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578523 | |||||||
| chrX:13578634 | G | A | 2 | a0001c0001t0002g0044 a0002c0003t0006g0043 |
2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.74+8699G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578634 | |||||||
| chrX:13578698 | A | G | 2 | a0001c0001t0002g0165 a0002c0002t0004g0215 |
2 | NA18956.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.74+8763A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578698 | |||||||
| chrX:13578710 | A | G | 192 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(189): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.74+8775A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578710 | |||||||
| chrX:13578758 | A | G | 25 | a0001c0001t0001g0024 a0001c0001t0001g0224 a0001c0001t0002g0027 others(22): Show |
25 | HG01106.hp1 HG01109.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.74+8823A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578758 | |||||||
| chrX:13578777 | C | T | 19 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(16): Show |
19 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+8842C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578777 | |||||||
| chrX:13578784 | T | TG | 20 | a0001c0001t0001g0224 a0001c0001t0001g0249 a0001c0001t0002g0045 others(17): Show |
20 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.74+8854dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13578784 | ||||||
| chrX:13578790 | C | G | 19 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(16): Show |
19 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+8855C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578790 | |||||||
| chrX:13578793 | C | G | 19 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(16): Show |
19 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+8858C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578793 | |||||||
| chrX:13578810 | G | A | 210 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.74+8875G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578810 | |||||||
| chrX:13578812 | T | G | 219 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(216): Show |
225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.74+8877T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578812 | |||||||
| chrX:13578848 | C | T | 1 | a0002c0003t0005g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.74+8913C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13578848 | |||||||
| chrX:13579060 | G | A | 9 | a0001c0001t0001g0024 a0001c0001t0002g0027 a0001c0001t0002g0044 others(6): Show |
10 | HG01109.hp1 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.74+9125G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579060 | |||||||
| chrX:13579156 | C | T | 210 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(207): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.74+9221C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579156 | |||||||
| chrX:13579247 | C | T | 19 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(16): Show |
19 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+9312C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579247 | |||||||
| chrX:13579312 | C | T | 19 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(16): Show |
19 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.74+9377C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579312 | |||||||
| chrX:13579676 | C | T | 210 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.74+9741C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579676 | |||||||
| chrX:13579766 | C | G | 12 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(9): Show |
12 | HG01106.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.75-9790C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579766 | |||||||
| chrX:13579820 | C | T | 8 | a0002c0003t0004g0031 a0002c0003t0004g0032 a0002c0003t0004g0033 others(5): Show |
8 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-9736C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579820 | |||||||
| chrX:13579928 | T | G | 1 | a0003c0006t0004g0291 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.75-9628T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579928 | |||||||
| chrX:13579995 | C | A | 1 | a0001c0001t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75-9561C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13579995 | |||||||
| chrX:13580072 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.75-9484C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13580072 | |||||||
| chrX:13580080 | T | C | 38 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0002g0098 others(35): Show |
40 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.75-9476T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13580080 | |||||||
| chrX:13580364 | C | T | 18 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0063 others(15): Show |
18 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.75-9192C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13580364 | |||||||
| chrX:13580365 | G | T | 20 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(17): Show |
20 | HG01106.hp1 HG01891.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.75-9191G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13580365 | |||||||
| chrX:13580908 | T | A | 1 | a0002c0002t0006g0104 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.75-8648T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13580908 | |||||||
| chrX:13581011 | G | A | 3 | a0001c0001t0002g0044 a0002c0003t0004g0002 a0002c0003t0006g0043 |
4 | HG01243.hp1 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-8545G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581011 | |||||||
| chrX:13581158 | A | G | 191 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0041 others(188): Show |
196 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.75-8398A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581158 | |||||||
| chrX:13581226 | G | A | 219 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(216): Show |
225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.75-8330G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581226 | |||||||
| chrX:13581286 | G | A | 2 | a0001c0008t0001g0296 a0010c0011t0004g0058 |
2 | HG02630.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.75-8270G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581286 | |||||||
| chrX:13581333 | C | A | 1 | a0001c0001t0001g0180 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.75-8223C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581333 | |||||||
| chrX:13581357 | C | G | 12 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(9): Show |
12 | HG01106.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.75-8199C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581357 | |||||||
| chrX:13581438 | T | TA | 12 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(9): Show |
12 | HG01106.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.75-8110dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13581438 | ||||||
| chrX:13581467 | G | A | 10 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(7): Show |
10 | HG01106.hp1 HG02451.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.75-8089G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581467 | |||||||
| chrX:13581499 | G | A | 117 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0001g0117 others(114): Show |
119 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.75-8057G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581499 | |||||||
| chrX:13581558 | A | G | 2 | a0002c0002t0004g0264 a0002c0002t0004g0265 |
2 | NA18968.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.75-7998A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581558 | |||||||
| chrX:13581962 | G | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0171 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-7594G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13581962 | |||||||
| chrX:13582061 | CT | C | 118 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0001g0117 others(115): Show |
120 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.75-7482delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13582061 | ||||||
| chrX:13582123 | C | T | 77 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0060 others(74): Show |
80 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.75-7433C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582123 | |||||||
| chrX:13582136 | G | C | 216 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(213): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.75-7420G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582136 | |||||||
| chrX:13582344 | G | A | 216 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(213): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.75-7212G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582344 | |||||||
| chrX:13582597 | G | A | 17 | a0001c0001t0001g0008 a0001c0001t0008g0012 a0001c0001t0008g0013 others(14): Show |
18 | HG00544.hp1 HG02155.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.75-6959G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582597 | |||||||
| chrX:13582738 | G | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0001g0117 others(116): Show |
121 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.75-6818G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582738 | |||||||
| chrX:13582746 | A | G | 120 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0001g0117 others(117): Show |
122 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.75-6810A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13582746 | |||||||
| chrX:13583073 | G | A | 19 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0063 others(16): Show |
19 | HG00639.hp1 HG01168.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.75-6483G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583073 | |||||||
| chrX:13583080 | C | T | 13 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(10): Show |
14 | HG00544.hp1 HG02155.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.75-6476C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583080 | |||||||
| chrX:13583207 | A | G | 1 | a0001c0001t0003g0103 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.75-6349A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583207 | |||||||
| chrX:13583648 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.75-5908A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583648 | |||||||
| chrX:13583695 | C | A | 1 | a0001c0001t0002g0105 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.75-5861C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583695 | |||||||
| chrX:13583987 | A | G | 1 | a0002c0002t0006g0156 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75-5569A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583987 | |||||||
| chrX:13583992 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75-5564G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13583992 | |||||||
| chrX:13584607 | A | G | 12 | a0001c0001t0008g0013 a0001c0001t0008g0014 a0001c0004t0001g0016 others(9): Show |
13 | HG00544.hp1 HG02155.hp2 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.75-4949A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13584607 | |||||||
| chrX:13584693 | C | T | 1 | a0002c0003t0007g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.75-4863C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13584693 | |||||||
| chrX:13584852 | T | C | 12 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(9): Show |
12 | HG01106.hp1 HG02451.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.75-4704T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13584852 | |||||||
| chrX:13584929 | C | T | 1 | a0001c0005t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.75-4627C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13584929 | |||||||
| chrX:13585027 | G | A | 1 | a0002c0003t0004g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75-4529G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585027 | |||||||
| chrX:13585149 | C | A | 1 | a0002c0003t0004g0002 | 2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.75-4407C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585149 | |||||||
| chrX:13585347 | C | T | 3 | a0001c0001t0002g0044 a0002c0003t0004g0002 a0002c0003t0006g0043 |
4 | HG01243.hp1 HG03453.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-4209C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585347 | |||||||
| chrX:13585755 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.75-3801C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585755 | |||||||
| chrX:13585756 | C | CT | 141 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0116 others(138): Show |
143 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.75-3800_75-3799ins others(1): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585756 | |||||||
| chrX:13585867 | G | A | 10 | a0001c0001t0001g0224 a0001c0001t0002g0045 a0001c0001t0003g0049 others(7): Show |
10 | HG01106.hp1 HG02451.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.75-3689G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585867 | |||||||
| chrX:13585908 | A | G | 3 | a0001c0001t0001g0041 a0001c0008t0001g0040 a0004c0021t0001g0042 |
3 | HG02647.hp1 HG02895.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.75-3648A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585908 | |||||||
| chrX:13585931 | C | T | 3 | a0001c0005t0001g0160 a0002c0003t0004g0158 a0002c0003t0004g0159 |
3 | HG01070.hp1 HG01074.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.75-3625C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13585931 | |||||||
| chrX:13586133 | C | T | 137 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0116 others(134): Show |
139 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.75-3423C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13586133 | |||||||
| chrX:13586166 | T | TATCATTA others(6): Show |
219 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(216): Show |
225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.75-3389_75-3388ins others(13): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | 13586166 | ||||||
| chrX:13586509 | C | G | 80 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0060 others(77): Show |
83 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.75-3047C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13586509 | |||||||
| chrX:13586647 | A | C | 18 | a0001c0001t0001g0024 a0001c0001t0001g0224 a0001c0001t0002g0027 others(15): Show |
18 | HG01106.hp1 HG01109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.75-2909A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13586647 | |||||||
| chrX:13586768 | T | G | 13 | a0001c0001t0008g0012 a0001c0001t0008g0013 a0001c0001t0008g0014 others(10): Show |
14 | HG00544.hp1 HG02155.hp2 HG03491.hp1 others(11): Show |
intron_variant | MODIFIER | c.75-2788T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13586768 | |||||||
| chrX:13586992 | G | T | 219 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(216): Show |
225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.75-2564G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13586992 | |||||||
| chrX:13587062 | A | G | 128 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0116 others(125): Show |
130 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.75-2494A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13587062 | |||||||
| chrX:13587558 | G | A | 3 | a0001c0001t0002g0045 a0001c0008t0001g0296 a0010c0011t0004g0058 |
3 | HG02630.hp2 HG03195.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.75-1998G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13587558 | |||||||
| chrX:13587673 | G | C | 2 | a0002c0003t0004g0002 a0002c0003t0006g0043 |
3 | HG01243.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.75-1883G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13587673 | |||||||
| chrX:13587682 | C | T | 2 | a0002c0003t0004g0002 a0002c0003t0006g0043 |
3 | HG01243.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.75-1874C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13587682 | |||||||
| chrX:13587851 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0002g0027 a0001c0001t0004g0025 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.75-1705G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13587851 | |||||||
| chrX:13588010 | A | G | 3 | a0001c0001t0002g0045 a0001c0008t0001g0296 a0010c0011t0004g0058 |
3 | HG02630.hp2 HG03195.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.75-1546A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588010 | |||||||
| chrX:13588192 | C | G | 219 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(216): Show |
225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.75-1364C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588192 | |||||||
| chrX:13588313 | G | A | 1 | a0002c0002t0006g0106 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.75-1243G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588313 | |||||||
| chrX:13588616 | C | T | 6 | a0001c0001t0001g0219 a0001c0001t0004g0223 a0001c0001t0004g0247 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.75-940C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588616 | |||||||
| chrX:13588684 | G | C | 1 | a0002c0003t0004g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.75-872G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588684 | |||||||
| chrX:13588687 | C | A | 2 | a0002c0003t0004g0002 a0002c0003t0006g0043 |
3 | HG01243.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.75-869C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588687 | |||||||
| chrX:13588725 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.75-831G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588725 | |||||||
| chrX:13588742 | C | T | 222 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(219): Show |
228 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.75-814C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588742 | |||||||
| chrX:13588784 | T | C | 2 | a0001c0001t0008g0013 a0001c0001t0008g0014 |
2 | NA18970.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.75-772T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588784 | |||||||
| chrX:13588821 | G | A | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.75-735G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13588821 | |||||||
| chrX:13589278 | A | G | 219 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(216): Show |
225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.75-278A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13589278 | |||||||
| chrX:13589303 | T | C | 219 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(216): Show |
225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.75-253T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 1/11 | chrX | 13589303 | |||||||
| chrX:13589725 | T | G | 1 | a0001c0001t0003g0227 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.187+57T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13589725 | |||||||
| chrX:13589762 | C | G | 124 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0116 others(121): Show |
126 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.187+94C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13589762 | |||||||
| chrX:13589844 | C | T | 8 | a0001c0001t0002g0068 a0001c0001t0002g0150 a0001c0001t0002g0151 others(5): Show |
8 | NA18944.hp1 NA18960.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.187+176C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13589844 | |||||||
| chrX:13589888 | A | T | 1 | a0002c0002t0007g0022 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.187+220A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13589888 | |||||||
| chrX:13589979 | G | A | 2 | a0001c0001t0003g0077 a0001c0017t0003g0078 |
2 | HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.187+311G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13589979 | |||||||
| chrX:13590006 | A | G | 210 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(207): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.187+338A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13590006 | |||||||
| chrX:13590383 | A | G | 9 | a0002c0003t0004g0002 a0002c0003t0004g0031 a0002c0003t0004g0032 others(6): Show |
10 | HG01243.hp1 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.187+715A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13590383 | |||||||
| chrX:13590618 | C | T | 3 | a0001c0001t0002g0045 a0002c0003t0004g0002 a0002c0003t0006g0043 |
4 | HG01243.hp1 HG03453.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+950C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13590618 | |||||||
| chrX:13590656 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.187+988C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13590656 | |||||||
| chrX:13591147 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.187+1479G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13591147 | |||||||
| chrX:13591328 | G | A | 3 | a0001c0001t0002g0045 a0002c0003t0004g0002 a0002c0003t0006g0043 |
4 | HG01243.hp1 HG03453.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.187+1660G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13591328 | |||||||
| chrX:13591368 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.187+1700G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13591368 | |||||||
| chrX:13592215 | T | TA | 83 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0060 others(80): Show |
86 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.187+2562dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592215 | ||||||
| chrX:13592236 | A | AT | 122 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0001g0117 others(119): Show |
124 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.187+2573dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592236 | ||||||
| chrX:13592306 | T | G | 3 | a0001c0005t0001g0055 a0001c0008t0001g0056 a0005c0012t0001g0054 |
3 | HG02293.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.188-2530T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592306 | |||||||
| chrX:13592553 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0002g0027 a0001c0001t0004g0025 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-2283G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592553 | |||||||
| chrX:13592706 | G | C | 10 | a0001c0001t0001g0292 a0001c0001t0002g0074 a0001c0001t0002g0108 others(7): Show |
10 | HG00544.hp2 HG02071.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.188-2130G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592706 | |||||||
| chrX:13592720 | T | G | 11 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(8): Show |
11 | HG02135.hp1 NA18940.hp1 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.188-2116T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592720 | |||||||
| chrX:13592723 | T | G | 7 | a0001c0001t0001g0024 a0001c0001t0002g0027 a0001c0001t0004g0025 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-2113T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592723 | |||||||
| chrX:13592870 | G | C | 16 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0002g0027 others(13): Show |
16 | HG01109.hp1 HG01891.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-1966G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592870 | |||||||
| chrX:13592911 | T | A | 26 | a0001c0001t0001g0060 a0001c0001t0001g0224 a0001c0001t0002g0044 others(23): Show |
27 | HG00544.hp1 HG02155.hp2 HG02486.hp1 others(24): Show |
intron_variant | MODIFIER | c.188-1925T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592911 | |||||||
| chrX:13592917 | C | CT | 118 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0116 others(115): Show |
120 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.188-1902dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592917 | ||||||
| chrX:13592917 | C | CTT | 32 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0216 others(29): Show |
33 | HG00544.hp1 HG01891.hp1 HG02132.hp1 others(30): Show |
intron_variant | MODIFIER | c.188-1903_188-1902d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13592917 | ||||||
| chrX:13592999 | C | T | 1 | a0001c0007t0003g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.188-1837C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13592999 | |||||||
| chrX:13593021 | TCTC | T | 97 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0001g0117 others(94): Show |
99 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.188-1812_188-1810d others(5): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13593021 | ||||||
| chrX:13593053 | T | TA | 7 | a0001c0001t0002g0068 a0001c0001t0002g0150 a0001c0001t0002g0151 others(4): Show |
7 | NA18960.hp1 NA18980.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-1782dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chrX | 13593053 | ||||||
| chrX:13593105 | T | C | 1 | a0010c0011t0004g0058 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.188-1731T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593105 | |||||||
| chrX:13593114 | T | C | 18 | a0001c0001t0001g0060 a0001c0001t0001g0216 a0001c0001t0002g0074 others(15): Show |
19 | HG00544.hp1 HG00544.hp2 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.188-1722T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593114 | |||||||
| chrX:13593124 | G | A | 1 | a0001c0001t0002g0128 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.188-1712G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593124 | |||||||
| chrX:13593153 | G | A | 62 | a0001c0001t0001g0071 a0001c0001t0001g0084 a0001c0001t0001g0161 others(59): Show |
64 | HG00544.hp2 HG00639.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.188-1683G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593153 | |||||||
| chrX:13593265 | G | A | 3 | a0001c0001t0001g0041 a0001c0008t0001g0040 a0002c0025t0004g0030 |
3 | HG02895.hp1 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.188-1571G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593265 | |||||||
| chrX:13593317 | A | G | 1 | a0012c0022t0001g0038 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.188-1519A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593317 | |||||||
| chrX:13593344 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.188-1492G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593344 | |||||||
| chrX:13593384 | G | C | 1 | a0001c0008t0001g0056 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.188-1452G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593384 | |||||||
| chrX:13593458 | C | G | 193 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(190): Show |
199 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.188-1378C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593458 | |||||||
| chrX:13593542 | T | G | 4 | a0001c0001t0002g0027 a0001c0001t0004g0025 a0002c0003t0007g0011 others(1): Show |
4 | HG01109.hp1 HG02970.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.188-1294T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593542 | |||||||
| chrX:13593611 | G | A | 2 | a0005c0013t0004g0029 a0005c0014t0001g0028 |
2 | HG02258.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.188-1225G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593611 | |||||||
| chrX:13593757 | G | A | 19 | a0001c0001t0001g0024 a0001c0001t0001g0219 a0001c0001t0001g0245 others(16): Show |
20 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.188-1079G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593757 | |||||||
| chrX:13593828 | A | T | 7 | a0005c0012t0001g0054 a0005c0013t0004g0029 a0005c0014t0001g0028 others(4): Show |
7 | HG02258.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-1008A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593828 | |||||||
| chrX:13593903 | G | A | 1 | a0002c0025t0004g0030 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.188-933G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593903 | |||||||
| chrX:13593905 | C | T | 1 | a0006c0009t0001g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.188-931C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593905 | |||||||
| chrX:13593977 | T | C | 3 | a0001c0001t0002g0027 a0001c0001t0004g0025 a0007c0016t0004g0026 |
3 | HG01109.hp1 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188-859T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13593977 | |||||||
| chrX:13594022 | G | C | 2 | a0001c0001t0002g0107 a0001c0001t0002g0122 |
2 | NA18950.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.188-814G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594022 | |||||||
| chrX:13594143 | C | A | 3 | a0001c0001t0002g0125 a0001c0001t0002g0131 a0001c0001t0002g0165 |
3 | NA18954.hp1 NA18956.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.188-693C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594143 | |||||||
| chrX:13594154 | T | C | 200 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(197): Show |
206 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.188-682T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594154 | |||||||
| chrX:13594362 | A | G | 2 | a0002c0003t0004g0164 a0009c0023t0001g0046 |
2 | HG02559.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.188-474A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594362 | |||||||
| chrX:13594403 | C | T | 200 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(197): Show |
206 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.188-433C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594403 | |||||||
| chrX:13594596 | T | C | 201 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(198): Show |
207 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.188-240T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594596 | |||||||
| chrX:13594666 | T | C | 3 | a0002c0003t0004g0031 a0002c0003t0004g0158 a0002c0003t0004g0159 |
3 | HG01070.hp1 HG01074.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.188-170T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594666 | |||||||
| chrX:13594739 | G | A | 1 | a0002c0003t0005g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.188-97G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594739 | |||||||
| chrX:13594740 | G | A | 1 | a0002c0003t0005g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.188-96G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594740 | |||||||
| chrX:13594761 | G | A | 1 | a0001c0008t0001g0056 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.188-75G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594761 | |||||||
| chrX:13594776 | G | A | 8 | a0001c0001t0001g0245 a0001c0001t0002g0098 a0001c0001t0003g0094 others(5): Show |
8 | HG02451.hp1 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.188-60G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 2/11 | chrX | 13594776 | |||||||
| chrX:13594942 | C | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0003g0091 others(2): Show |
5 | HG01496.hp2 HG01517.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+14C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13594942 | |||||||
| chrX:13594963 | C | T | 2 | a0001c0008t0001g0296 a0002c0024t0004g0266 |
2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.280+35C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13594963 | |||||||
| chrX:13595000 | G | C | 1 | a0001c0001t0002g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.280+72G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595000 | |||||||
| chrX:13595216 | G | A | 1 | a0001c0008t0001g0056 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.280+288G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595216 | |||||||
| chrX:13595235 | C | G | 1 | a0001c0001t0002g0157 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.280+307C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595235 | |||||||
| chrX:13595276 | C | A | 5 | a0001c0005t0001g0057 a0001c0008t0001g0056 a0001c0008t0001g0296 others(2): Show |
5 | HG01106.hp1 HG02293.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+348C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595276 | |||||||
| chrX:13595619 | C | A | 5 | a0001c0008t0001g0056 a0001c0008t0001g0296 a0002c0003t0004g0037 others(2): Show |
5 | HG02293.hp1 HG02647.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+691C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595619 | |||||||
| chrX:13595722 | C | CT | 19 | a0001c0001t0002g0027 a0001c0001t0004g0025 a0001c0005t0001g0057 others(16): Show |
19 | HG01106.hp1 HG01109.hp1 HG02293.hp1 others(16): Show |
intron_variant | MODIFIER | c.280+809dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13595722 | ||||||
| chrX:13595968 | C | T | 5 | a0002c0003t0004g0031 a0002c0003t0004g0158 a0002c0003t0004g0159 others(2): Show |
5 | HG01070.hp1 HG01074.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+1040C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13595968 | |||||||
| chrX:13596349 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.280+1421T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596349 | |||||||
| chrX:13596366 | C | T | 1 | a0002c0003t0004g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.280+1438C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596366 | |||||||
| chrX:13596372 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.280+1444C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596372 | |||||||
| chrX:13596869 | C | G | 1 | a0003c0006t0004g0291 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.280+1941C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596869 | |||||||
| chrX:13596999 | A | G | 236 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(233): Show |
242 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.280+2071A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13596999 | |||||||
| chrX:13597066 | T | C | 1 | a0001c0001t0002g0155 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.280+2138T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597066 | |||||||
| chrX:13597107 | G | A | 162 | a0001c0001t0001g0006 a0001c0001t0001g0072 a0001c0001t0001g0084 others(159): Show |
166 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.280+2179G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597107 | |||||||
| chrX:13597149 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.280+2221C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597149 | |||||||
| chrX:13597276 | A | G | 3 | a0002c0003t0004g0032 a0002c0003t0004g0033 a0002c0003t0004g0169 |
3 | HG01891.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.280+2348A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597276 | |||||||
| chrX:13597326 | C | G | 1 | a0001c0001t0003g0212 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.280+2398C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597326 | |||||||
| chrX:13597357 | G | A | 1 | a0010c0011t0004g0058 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.280+2429G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597357 | |||||||
| chrX:13597407 | C | T | 1 | a0001c0001t0010g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.280+2479C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597407 | |||||||
| chrX:13597492 | C | T | 1 | a0001c0018t0002g0067 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.281-2483C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597492 | |||||||
| chrX:13597510 | A | G | 1 | a0001c0001t0010g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.281-2465A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597510 | |||||||
| chrX:13597546 | G | C | 108 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0041 others(105): Show |
111 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(108): Show |
intron_variant | MODIFIER | c.281-2429G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597546 | |||||||
| chrX:13597548 | T | C | 225 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(222): Show |
231 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.281-2427T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597548 | |||||||
| chrX:13597549 | C | T | 222 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0024 others(219): Show |
228 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.281-2426C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597549 | |||||||
| chrX:13597558 | T | C | 2 | a0002c0003t0007g0011 a0007c0016t0004g0026 |
2 | HG01109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.281-2417T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597558 | |||||||
| chrX:13597612 | C | T | 1 | a0001c0001t0002g0155 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.281-2363C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597612 | |||||||
| chrX:13597613 | A | G | 1 | a0001c0001t0002g0155 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.281-2362A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597613 | |||||||
| chrX:13597644 | C | T | 1 | a0001c0001t0003g0227 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.281-2331C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597644 | |||||||
| chrX:13597654 | A | C | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | NA18946.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.281-2321A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597654 | |||||||
| chrX:13597783 | C | CA | 50 | a0001c0001t0001g0202 a0001c0001t0002g0039 a0001c0001t0002g0098 others(47): Show |
53 | HG00544.hp1 HG00735.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.281-2191dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13597783 | ||||||
| chrX:13597784 | AG | A | 5 | a0001c0001t0002g0125 a0001c0001t0002g0137 a0001c0001t0002g0151 others(2): Show |
5 | NA18954.hp1 NA18955.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-2190delG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597784 | |||||||
| chrX:13597785 | G | A | 200 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(197): Show |
206 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.281-2190G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597785 | |||||||
| chrX:13597788 | A | G | 1 | a0001c0001t0003g0099 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.281-2187A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597788 | |||||||
| chrX:13597982 | T | C | 1 | a0009c0023t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.281-1993T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597982 | |||||||
| chrX:13597994 | T | C | 5 | a0001c0005t0001g0057 a0002c0025t0004g0030 a0006c0009t0001g0283 others(2): Show |
5 | HG01106.hp1 HG02280.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-1981T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13597994 | |||||||
| chrX:13598234 | G | C | 1 | a0002c0003t0006g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.281-1741G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598234 | |||||||
| chrX:13598249 | A | G | 2 | a0001c0001t0002g0163 a0009c0023t0001g0046 |
2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.281-1726A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598249 | |||||||
| chrX:13598273 | G | C | 1 | a0001c0001t0001g0259 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.281-1702G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598273 | |||||||
| chrX:13598275 | G | C | 1 | a0001c0001t0003g0079 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.281-1700G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598275 | |||||||
| chrX:13598558 | A | AGTT | 11 | a0001c0001t0001g0219 a0001c0001t0003g0094 a0001c0004t0004g0059 others(8): Show |
11 | HG02280.hp2 HG02572.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-1386_281-1384d others(5): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598558 | ||||||
| chrX:13598558 | AGTT | A | 5 | a0001c0001t0001g0281 a0001c0001t0002g0243 a0002c0003t0004g0033 others(2): Show |
5 | HG01175.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-1386_281-1384d others(5): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598558 | ||||||
| chrX:13598558 | AGTTGTT | A | 128 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(125): Show |
130 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.281-1389_281-1384d others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598558 | ||||||
| chrX:13598558 | AGTTGTTG others(8): Show |
A | 1 | a0001c0001t0002g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.281-1398_281-1384d others(17): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598558 | ||||||
| chrX:13598691 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.281-1284T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598691 | |||||||
| chrX:13598761 | G | A | 1 | a0001c0001t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.281-1214G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598761 | |||||||
| chrX:13598784 | G | A | 7 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0203 others(4): Show |
7 | HG00408.hp1 HG00609.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-1191G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598784 | |||||||
| chrX:13598863 | C | CAT | 217 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(214): Show |
223 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.281-1105_281-1104d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598863 | ||||||
| chrX:13598863 | C | CATATATA others(75): Show |
1 | a0001c0001t0003g0083 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.281-1104_281-1103i others(84): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598863 | ||||||
| chrX:13598863 | C | CATATATA others(34): Show |
3 | a0002c0003t0004g0032 a0002c0003t0004g0033 a0002c0003t0004g0169 |
3 | HG01891.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.281-1062_281-1022d others(43): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598863 | ||||||
| chrX:13598954 | A | T | 2 | a0001c0001t0003g0094 a0001c0004t0004g0059 |
2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.281-1021A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598954 | |||||||
| chrX:13598956 | A | T | 5 | a0001c0001t0001g0219 a0001c0001t0003g0094 a0001c0004t0004g0059 others(2): Show |
5 | HG02572.hp1 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-1019A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598956 | |||||||
| chrX:13598958 | A | ATATATAA others(33): Show |
1 | a0007c0016t0004g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-1016_281-1015i others(42): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chrX | 13598958 | ||||||
| chrX:13598958 | A | T | 55 | a0001c0001t0001g0219 a0001c0001t0001g0268 a0001c0001t0001g0269 others(52): Show |
57 | HG00544.hp1 HG00621.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.281-1017A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598958 | |||||||
| chrX:13598965 | T | A | 3 | a0002c0003t0004g0031 a0002c0003t0004g0158 a0004c0020t0001g0047 |
3 | HG01070.hp1 HG02486.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.281-1010T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13598965 | |||||||
| chrX:13599193 | T | G | 44 | a0001c0001t0001g0195 a0001c0001t0001g0219 a0001c0001t0003g0094 others(41): Show |
46 | HG00544.hp1 HG00735.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.281-782T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13599193 | |||||||
| chrX:13599524 | G | A | 2 | a0002c0003t0004g0037 a0007c0016t0004g0026 |
2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.281-451G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13599524 | |||||||
| chrX:13599644 | T | C | 5 | a0001c0001t0001g0060 a0001c0001t0002g0098 a0002c0003t0004g0031 others(2): Show |
5 | HG01070.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-331T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13599644 | |||||||
| chrX:13599852 | G | A | 4 | a0001c0001t0002g0044 a0002c0003t0004g0032 a0002c0003t0004g0033 others(1): Show |
4 | HG01891.hp1 HG03540.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-123G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13599852 | |||||||
| chrX:13599866 | T | C | 3 | a0001c0004t0002g0132 a0001c0004t0002g0133 a0001c0004t0002g0134 |
3 | NA19057.hp1 NA19072.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.281-109T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 3/11 | chrX | 13599866 | |||||||
| chrX:13600164 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0206 |
2 | NA18972.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.400+70G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600164 | |||||||
| chrX:13600266 | C | CTTCT | 40 | a0001c0001t0001g0060 a0001c0001t0001g0195 a0001c0001t0002g0065 others(37): Show |
42 | HG00544.hp1 HG00735.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.400+182_400+185dup others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600266 | ||||||
| chrX:13600274 | T | TTTCTTTC | 7 | a0001c0001t0003g0083 a0002c0003t0004g0169 a0002c0025t0004g0030 others(4): Show |
7 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.400+185_400+186ins others(7): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600274 | ||||||
| chrX:13600277 | C | CT | 5 | a0002c0003t0004g0031 a0002c0003t0004g0037 a0002c0003t0004g0158 others(2): Show |
5 | HG01070.hp1 HG01109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+185dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600277 | ||||||
| chrX:13600277 | C | CTTTCTTC others(1): Show |
7 | a0001c0005t0001g0055 a0001c0005t0001g0225 a0001c0005t0001g0244 others(4): Show |
8 | HG01243.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.400+185_400+186ins others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600277 | ||||||
| chrX:13600277 | C | CTTTCTTC others(2): Show |
3 | a0001c0005t0001g0160 a0001c0005t0001g0220 a0001c0005t0001g0280 |
3 | HG02145.hp1 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.400+185_400+186ins others(9): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600277 | ||||||
| chrX:13600277 | C | CTTTCTTC others(3): Show |
1 | a0001c0005t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.400+185_400+186ins others(10): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600277 | ||||||
| chrX:13600278 | T | TTTCTTC | 41 | a0001c0001t0001g0174 a0001c0001t0001g0182 a0001c0001t0001g0185 others(38): Show |
42 | HG00639.hp2 HG00738.hp1 HG01433.hp1 others(39): Show |
intron_variant | MODIFIER | c.400+185_400+186ins others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600278 | ||||||
| chrX:13600279 | T | TTCTTC | 111 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(108): Show |
113 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.400+185_400+186ins others(5): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600279 | |||||||
| chrX:13600280 | C | CT | 9 | a0001c0001t0001g0063 a0001c0001t0001g0172 a0001c0001t0001g0186 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.400+210dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600280 | ||||||
| chrX:13600280 | C | T | 170 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(167): Show |
174 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.400+186C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600280 | |||||||
| chrX:13600285 | T | C | 1 | a0004c0021t0001g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.400+191T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600285 | |||||||
| chrX:13600288 | T | C | 1 | a0004c0021t0001g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.400+194T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600288 | |||||||
| chrX:13600390 | A | G | 216 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(213): Show |
222 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.400+296A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600390 | |||||||
| chrX:13600436 | G | T | 1 | a0009c0023t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.400+342G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600436 | |||||||
| chrX:13600444 | G | A | 4 | a0001c0001t0001g0060 a0002c0003t0004g0031 a0002c0003t0004g0158 others(1): Show |
4 | HG01070.hp1 HG02486.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+350G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600444 | |||||||
| chrX:13600634 | A | G | 8 | a0001c0007t0001g0274 a0001c0007t0003g0101 a0001c0007t0003g0177 others(5): Show |
9 | HG01243.hp1 HG02027.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.400+540A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600634 | |||||||
| chrX:13600718 | C | T | 2 | a0002c0003t0004g0037 a0007c0016t0004g0026 |
2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.400+624C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600718 | |||||||
| chrX:13600735 | T | TA | 22 | a0001c0001t0001g0060 a0001c0001t0001g0252 a0001c0005t0001g0057 others(19): Show |
23 | HG01070.hp1 HG01106.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.400+659dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600735 | ||||||
| chrX:13600745 | A | G | 7 | a0001c0001t0001g0202 a0001c0001t0001g0231 a0001c0001t0001g0237 others(4): Show |
7 | HG01975.hp2 NA18975.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.400+651A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600745 | |||||||
| chrX:13600753 | A | AAT | 44 | a0001c0001t0001g0195 a0001c0001t0001g0219 a0001c0001t0002g0098 others(41): Show |
46 | HG00544.hp1 HG00735.hp2 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.400+659_400+660ins others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600753 | |||||||
| chrX:13600780 | G | T | 4 | a0001c0001t0002g0044 a0002c0003t0004g0032 a0002c0003t0004g0033 others(1): Show |
4 | HG01891.hp1 HG03540.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.400+686G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600780 | |||||||
| chrX:13600795 | G | GA | 9 | a0001c0005t0001g0055 a0001c0005t0001g0160 a0001c0005t0001g0220 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.400+704dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chrX | 13600795 | ||||||
| chrX:13600799 | G | A | 13 | a0001c0005t0001g0055 a0001c0005t0001g0057 a0001c0005t0001g0160 others(10): Show |
13 | HG01106.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.400+705G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600799 | |||||||
| chrX:13600822 | T | C | 11 | a0001c0001t0002g0044 a0001c0007t0001g0274 a0001c0007t0003g0101 others(8): Show |
12 | HG01243.hp1 HG01891.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+728T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600822 | |||||||
| chrX:13600909 | G | T | 1 | a0009c0023t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.400+815G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13600909 | |||||||
| chrX:13601081 | A | G | 1 | a0009c0023t0001g0046 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.400+987A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601081 | |||||||
| chrX:13601186 | A | C | 22 | a0001c0005t0001g0055 a0001c0005t0001g0057 a0001c0005t0001g0160 others(19): Show |
22 | HG01106.hp1 HG01891.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.400+1092A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601186 | |||||||
| chrX:13601399 | T | C | 1 | a0001c0004t0001g0069 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.400+1305T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601399 | |||||||
| chrX:13601573 | T | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0249 a0001c0001t0002g0136 others(1): Show |
4 | NA18967.hp1 NA18978.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.400+1479T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601573 | |||||||
| chrX:13601634 | C | G | 1 | a0007c0016t0004g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.400+1540C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601634 | |||||||
| chrX:13601645 | G | A | 5 | a0001c0001t0004g0223 a0001c0001t0004g0247 a0002c0003t0004g0284 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.400+1551G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601645 | |||||||
| chrX:13601866 | T | C | 1 | a0001c0004t0001g0069 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.401-1451T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601866 | |||||||
| chrX:13601869 | T | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0003g0162 |
3 | HG02257.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.401-1448T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601869 | |||||||
| chrX:13601889 | A | G | 5 | a0001c0007t0001g0274 a0001c0007t0003g0101 a0001c0007t0003g0177 others(2): Show |
5 | HG02027.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-1428A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13601889 | |||||||
| chrX:13602174 | C | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0208 a0001c0001t0001g0211 |
4 | HG00323.hp2 HG01192.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.401-1143C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602174 | |||||||
| chrX:13602257 | G | A | 14 | a0001c0005t0001g0055 a0001c0005t0001g0057 a0001c0005t0001g0160 others(11): Show |
14 | HG01106.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.401-1060G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602257 | |||||||
| chrX:13602344 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0002g0139 |
2 | NA18945.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.401-973T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602344 | |||||||
| chrX:13602548 | C | T | 1 | a0002c0002t0006g0135 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.401-769C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602548 | |||||||
| chrX:13602820 | G | A | 4 | a0001c0001t0009g0214 a0003c0006t0002g0138 a0003c0006t0004g0291 others(1): Show |
5 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-497G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602820 | |||||||
| chrX:13602963 | C | T | 4 | a0001c0001t0009g0214 a0003c0006t0002g0138 a0003c0006t0004g0291 others(1): Show |
5 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-354C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602963 | |||||||
| chrX:13602974 | A | T | 5 | a0001c0001t0009g0214 a0003c0006t0002g0129 a0003c0006t0002g0138 others(2): Show |
6 | HG01975.hp1 HG02004.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-343A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 4/11 | chrX | 13602974 | |||||||
| chrX:13603517 | A | G | 1 | a0001c0001t0002g0149 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.520+81A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13603517 | |||||||
| chrX:13603820 | C | T | 1 | a0004c0021t0001g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.520+384C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13603820 | |||||||
| chrX:13603857 | A | G | 1 | a0002c0003t0006g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.520+421A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13603857 | |||||||
| chrX:13603980 | A | G | 136 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(133): Show |
139 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.520+544A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13603980 | |||||||
| chrX:13604187 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.520+751A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13604187 | |||||||
| chrX:13604675 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.520+1239T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13604675 | |||||||
| chrX:13605047 | CT | C | 134 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(131): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.521-1327delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605047 | ||||||
| chrX:13605054 | G | T | 134 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(131): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.521-1325G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605054 | |||||||
| chrX:13605359 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.521-1020A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605359 | |||||||
| chrX:13605459 | G | C | 1 | a0004c0021t0001g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.521-920G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605459 | |||||||
| chrX:13605509 | A | G | 4 | a0001c0001t0009g0214 a0003c0006t0002g0138 a0003c0006t0004g0291 others(1): Show |
5 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.521-870A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605509 | |||||||
| chrX:13605578 | C | CA | 67 | a0001c0001t0001g0006 a0001c0001t0001g0060 a0001c0001t0001g0062 others(64): Show |
68 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.521-781dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605578 | ||||||
| chrX:13605578 | CA | C | 11 | a0001c0001t0001g0171 a0001c0001t0001g0210 a0001c0001t0001g0263 others(8): Show |
11 | HG01069.hp1 HG01169.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.521-781delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605578 | ||||||
| chrX:13605578 | CAAA | C | 46 | a0001c0001t0001g0219 a0001c0001t0003g0094 a0001c0001t0005g0051 others(43): Show |
49 | HG00544.hp1 HG00735.hp2 HG01167.hp1 others(46): Show |
intron_variant | MODIFIER | c.521-783_521-781del others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chrX | 13605578 | ||||||
| chrX:13605599 | G | A | 1 | a0001c0001t0003g0227 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.521-780G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605599 | |||||||
| chrX:13605828 | C | T | 7 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0257 others(4): Show |
7 | HG00597.hp2 HG02071.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.521-551C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605828 | |||||||
| chrX:13605857 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.521-522C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605857 | |||||||
| chrX:13605982 | C | T | 3 | a0001c0001t0002g0068 a0001c0001t0002g0113 a0001c0001t0002g0114 |
3 | NA18975.hp2 NA18998.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.521-397C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13605982 | |||||||
| chrX:13606159 | T | C | 2 | a0002c0003t0004g0002 a0002c0003t0004g0164 |
3 | HG01243.hp1 HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.521-220T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13606159 | |||||||
| chrX:13606163 | G | A | 54 | a0001c0001t0001g0060 a0001c0001t0001g0219 a0001c0001t0002g0098 others(51): Show |
56 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.521-216G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13606163 | |||||||
| chrX:13606286 | C | G | 1 | a0001c0001t0002g0184 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.521-93C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 5/11 | chrX | 13606286 | |||||||
| chrX:13606522 | C | T | 5 | a0001c0007t0001g0274 a0001c0007t0003g0101 a0001c0007t0003g0177 others(2): Show |
5 | HG02027.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+9C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13606522 | |||||||
| chrX:13606627 | G | C | 1 | a0001c0001t0002g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.655+114G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13606627 | |||||||
| chrX:13607264 | C | G | 2 | a0002c0003t0004g0234 a0009c0023t0001g0046 |
2 | HG02559.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.655+751C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607264 | |||||||
| chrX:13607283 | C | T | 1 | a0008c0015t0007g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.655+770C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607283 | |||||||
| chrX:13607291 | G | A | 1 | a0002c0003t0004g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.655+778G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607291 | |||||||
| chrX:13607357 | C | T | 4 | a0001c0001t0009g0214 a0003c0006t0002g0138 a0003c0006t0004g0291 others(1): Show |
5 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+844C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607357 | |||||||
| chrX:13607426 | C | T | 1 | a0002c0003t0006g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.656-898C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607426 | |||||||
| chrX:13607434 | C | T | 53 | a0001c0001t0001g0060 a0001c0001t0001g0219 a0001c0001t0002g0098 others(50): Show |
55 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.656-890C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607434 | |||||||
| chrX:13607928 | G | A | 6 | a0002c0003t0004g0031 a0002c0003t0004g0158 a0002c0025t0004g0030 others(3): Show |
6 | HG01070.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-396G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607928 | |||||||
| chrX:13607934 | G | A | 16 | a0001c0005t0001g0055 a0001c0005t0001g0160 a0001c0005t0001g0220 others(13): Show |
16 | HG01070.hp1 HG01109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.656-390G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13607934 | |||||||
| chrX:13608033 | G | A | 89 | a0001c0001t0001g0060 a0001c0001t0001g0219 a0001c0001t0002g0098 others(86): Show |
92 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.656-291G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13608033 | |||||||
| chrX:13608051 | C | T | 1 | a0001c0004t0002g0134 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.656-273C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13608051 | |||||||
| chrX:13608196 | C | T | 1 | a0001c0001t0010g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.656-128C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13608196 | |||||||
| chrX:13608284 | T | C | 87 | a0001c0001t0001g0060 a0001c0001t0001g0219 a0001c0001t0002g0098 others(84): Show |
90 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.656-40T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 6/11 | chrX | 13608284 | |||||||
| chrX:13608480 | T | G | 5 | a0001c0007t0001g0274 a0001c0007t0003g0101 a0001c0007t0003g0177 others(2): Show |
5 | HG02027.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.778+34T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13608480 | |||||||
| chrX:13608501 | A | G | 9 | a0001c0001t0001g0228 a0001c0001t0001g0239 a0001c0001t0001g0250 others(6): Show |
9 | HG00639.hp2 HG01168.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.778+55A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13608501 | |||||||
| chrX:13608755 | T | A | 10 | a0001c0001t0002g0131 a0001c0001t0002g0137 a0001c0001t0002g0150 others(7): Show |
11 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.778+309T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13608755 | |||||||
| chrX:13609169 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.778+723G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13609169 | |||||||
| chrX:13609728 | T | C | 46 | a0001c0001t0001g0219 a0001c0001t0002g0098 a0001c0001t0003g0094 others(43): Show |
48 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.778+1282T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13609728 | |||||||
| chrX:13610917 | T | C | 26 | a0001c0001t0001g0007 a0001c0001t0001g0187 a0001c0001t0001g0192 others(23): Show |
26 | HG00597.hp2 HG00642.hp1 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.778+2471T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13610917 | |||||||
| chrX:13611142 | G | A | 21 | a0001c0001t0009g0214 a0001c0005t0001g0055 a0001c0005t0001g0057 others(18): Show |
22 | HG01070.hp1 HG01106.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.778+2696G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13611142 | |||||||
| chrX:13611302 | G | T | 4 | a0001c0007t0001g0274 a0001c0007t0003g0101 a0001c0007t0003g0177 others(1): Show |
4 | HG02027.hp1 HG02723.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.778+2856G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13611302 | |||||||
| chrX:13611391 | A | G | 4 | a0002c0003t0004g0032 a0002c0003t0004g0033 a0002c0003t0004g0169 others(1): Show |
4 | HG01891.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.778+2945A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13611391 | |||||||
| chrX:13611403 | C | T | 53 | a0001c0001t0001g0060 a0001c0001t0001g0219 a0001c0001t0002g0098 others(50): Show |
55 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.778+2957C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13611403 | |||||||
| chrX:13611860 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.778+3414T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13611860 | |||||||
| chrX:13612007 | T | C | 5 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0008t0001g0040 others(2): Show |
5 | HG02293.hp1 HG02895.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.778+3561T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612007 | |||||||
| chrX:13612026 | T | C | 85 | a0001c0001t0001g0060 a0001c0001t0001g0219 a0001c0001t0002g0098 others(82): Show |
88 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(85): Show |
intron_variant | MODIFIER | c.778+3580T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612026 | |||||||
| chrX:13612048 | T | A | 1 | a0001c0001t0009g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.778+3602T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612048 | |||||||
| chrX:13612049 | T | A | 12 | a0001c0001t0002g0105 a0001c0001t0009g0214 a0001c0007t0001g0274 others(9): Show |
13 | HG01258.hp1 HG01975.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.778+3603T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612049 | |||||||
| chrX:13612050 | A | T | 35 | a0001c0001t0002g0061 a0001c0001t0003g0179 a0001c0004t0001g0016 others(32): Show |
37 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.778+3604A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612050 | |||||||
| chrX:13612323 | T | G | 2 | a0004c0020t0001g0047 a0010c0011t0004g0058 |
2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.778+3877T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612323 | |||||||
| chrX:13612324 | A | G | 3 | a0001c0001t0001g0240 a0001c0001t0001g0263 a0001c0001t0001g0270 |
3 | NA18957.hp2 NA18980.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.778+3878A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612324 | |||||||
| chrX:13612459 | A | G | 16 | a0001c0005t0001g0055 a0001c0005t0001g0057 a0001c0005t0001g0160 others(13): Show |
16 | HG01070.hp1 HG01106.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.778+4013A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612459 | |||||||
| chrX:13612540 | C | T | 1 | a0001c0001t0003g0088 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.778+4094C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612540 | |||||||
| chrX:13612567 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.778+4121T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612567 | |||||||
| chrX:13612574 | C | CG | 6 | a0001c0001t0001g0072 a0001c0001t0001g0194 a0001c0001t0001g0275 others(3): Show |
6 | HG01109.hp1 HG01175.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+4132dupG | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13612574 | ||||||
| chrX:13612583 | G | A | 47 | a0001c0001t0001g0219 a0001c0001t0003g0094 a0001c0001t0003g0179 others(44): Show |
49 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.778+4137G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612583 | |||||||
| chrX:13612586 | C | T | 6 | a0001c0007t0001g0274 a0001c0007t0003g0101 a0001c0007t0003g0177 others(3): Show |
6 | HG02027.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+4140C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612586 | |||||||
| chrX:13612620 | G | A | 6 | a0001c0007t0001g0274 a0001c0007t0003g0101 a0001c0007t0003g0177 others(3): Show |
6 | HG02027.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.778+4174G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612620 | |||||||
| chrX:13612670 | G | T | 15 | a0001c0005t0001g0055 a0001c0005t0001g0160 a0001c0005t0001g0220 others(12): Show |
15 | HG01070.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.778+4224G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612670 | |||||||
| chrX:13612687 | C | T | 7 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0001c0008t0001g0040 others(4): Show |
7 | HG02293.hp1 HG02895.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.778+4241C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612687 | |||||||
| chrX:13612814 | C | T | 35 | a0001c0001t0003g0179 a0001c0004t0001g0016 a0001c0004t0001g0069 others(32): Show |
37 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.778+4368C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612814 | |||||||
| chrX:13612947 | C | T | 1 | a0001c0001t0002g0115 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.778+4501C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13612947 | |||||||
| chrX:13613018 | G | A | 1 | a0002c0003t0004g0234 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.778+4572G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613018 | |||||||
| chrX:13613123 | C | T | 2 | a0004c0021t0001g0042 a0009c0023t0001g0046 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.779-4607C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613123 | |||||||
| chrX:13613157 | C | CAT | 111 | a0001c0001t0001g0006 a0001c0001t0001g0062 a0001c0001t0001g0072 others(108): Show |
115 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.779-4552_779-4551d others(4): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613157 | C | CATAT | 12 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0189 others(9): Show |
12 | HG00323.hp2 HG01192.hp1 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.779-4554_779-4551d others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613157 | C | CATATAT | 13 | a0001c0005t0001g0057 a0001c0005t0001g0160 a0001c0005t0001g0220 others(10): Show |
13 | HG01070.hp1 HG01106.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.779-4556_779-4551d others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613157 | C | CATATATA others(3): Show |
3 | a0002c0003t0004g0032 a0002c0003t0004g0169 a0005c0014t0001g0028 |
3 | HG01891.hp1 HG02258.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.779-4560_779-4551d others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613157 | C | CATATATA others(5): Show |
1 | a0002c0003t0006g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.779-4562_779-4551d others(14): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613157 | C | CATATATA others(7): Show |
1 | a0002c0003t0004g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.779-4564_779-4551d others(16): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613157 | C | CATATATA others(11): Show |
4 | a0001c0007t0001g0274 a0001c0008t0001g0056 a0001c0008t0001g0296 others(1): Show |
4 | HG02293.hp1 HG02723.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.779-4568_779-4551d others(20): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613157 | C | CATATATA others(13): Show |
8 | a0001c0001t0004g0223 a0001c0001t0004g0247 a0001c0001t0005g0050 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.779-4570_779-4551d others(22): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613157 | C | CATATATA others(15): Show |
6 | a0001c0001t0001g0060 a0002c0003t0004g0037 a0002c0003t0004g0234 others(3): Show |
6 | HG01109.hp1 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.779-4572_779-4551d others(24): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613157 | C | CATATATA others(25): Show |
1 | a0002c0024t0004g0266 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.779-4551_779-4550i others(34): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613157 | CATATATA others(3): Show |
C | 6 | a0001c0001t0001g0219 a0001c0001t0002g0098 a0001c0001t0003g0094 others(3): Show |
6 | HG02572.hp1 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.779-4560_779-4551d others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13613157 | ||||||
| chrX:13613179 | T | TATATATA others(12): Show |
1 | a0001c0001t0005g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.779-4551_779-4550i others(21): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613179 | |||||||
| chrX:13613245 | A | T | 1 | a0002c0003t0006g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.779-4485A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613245 | |||||||
| chrX:13613531 | C | T | 1 | a0001c0001t0003g0023 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.779-4199C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13613531 | |||||||
| chrX:13614161 | G | A | 2 | a0001c0001t0003g0082 a0001c0001t0003g0294 |
2 | HG04184.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.779-3569G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614161 | |||||||
| chrX:13614338 | T | C | 1 | a0002c0003t0006g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.779-3392T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614338 | |||||||
| chrX:13614508 | G | T | 1 | a0001c0005t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.779-3222G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614508 | |||||||
| chrX:13614673 | G | A | 1 | a0001c0001t0010g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.779-3057G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614673 | |||||||
| chrX:13614749 | A | AT | 60 | a0001c0001t0001g0219 a0001c0001t0002g0098 a0001c0001t0002g0114 others(57): Show |
64 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.779-2965dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13614749 | ||||||
| chrX:13614749 | ATTTT | A | 9 | a0001c0005t0001g0055 a0001c0005t0001g0160 a0001c0005t0001g0220 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.779-2968_779-2965d others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13614749 | ||||||
| chrX:13614751 | T | TA | 6 | a0001c0007t0001g0274 a0001c0007t0003g0101 a0001c0007t0003g0177 others(3): Show |
6 | HG02027.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.779-2979_779-2978i others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614751 | |||||||
| chrX:13614947 | G | T | 168 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(165): Show |
172 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.779-2783G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13614947 | |||||||
| chrX:13615124 | G | A | 2 | a0002c0003t0004g0037 a0007c0016t0004g0026 |
2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.779-2606G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615124 | |||||||
| chrX:13615224 | T | C | 1 | a0001c0001t0003g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.779-2506T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615224 | |||||||
| chrX:13615456 | C | G | 1 | a0001c0004t0003g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.779-2274C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615456 | |||||||
| chrX:13615479 | C | T | 6 | a0001c0007t0001g0274 a0001c0007t0003g0101 a0001c0007t0003g0177 others(3): Show |
6 | HG02027.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.779-2251C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615479 | |||||||
| chrX:13615490 | G | A | 158 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(155): Show |
162 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.779-2240G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615490 | |||||||
| chrX:13615654 | T | C | 2 | a0004c0020t0001g0047 a0010c0011t0004g0058 |
2 | HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.779-2076T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615654 | |||||||
| chrX:13615710 | T | C | 1 | a0001c0001t0003g0168 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.779-2020T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615710 | |||||||
| chrX:13615838 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.779-1892A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615838 | |||||||
| chrX:13615998 | A | T | 2 | a0002c0003t0004g0037 a0007c0016t0004g0026 |
2 | HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.779-1732A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13615998 | |||||||
| chrX:13616064 | T | C | 48 | a0001c0001t0001g0219 a0001c0001t0002g0098 a0001c0001t0003g0094 others(45): Show |
50 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.779-1666T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616064 | |||||||
| chrX:13616196 | C | T | 4 | a0001c0001t0009g0214 a0003c0006t0002g0138 a0003c0006t0004g0291 others(1): Show |
5 | HG01975.hp1 HG02132.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.779-1534C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616196 | |||||||
| chrX:13616243 | G | C | 13 | a0001c0001t0009g0214 a0001c0005t0001g0055 a0001c0005t0001g0160 others(10): Show |
14 | HG01975.hp1 HG02132.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.779-1487G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616243 | |||||||
| chrX:13616480 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.779-1250C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616480 | |||||||
| chrX:13616514 | G | A | 123 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(120): Show |
126 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.779-1216G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616514 | |||||||
| chrX:13616662 | A | G | 1 | a0001c0005t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.779-1068A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616662 | |||||||
| chrX:13616683 | C | T | 1 | a0002c0003t0006g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.779-1047C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616683 | |||||||
| chrX:13616772 | T | G | 1 | a0001c0007t0001g0274 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.779-958T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616772 | |||||||
| chrX:13616783 | C | G | 9 | a0001c0001t0001g0060 a0001c0007t0001g0274 a0001c0007t0003g0101 others(6): Show |
9 | HG02027.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.779-947C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616783 | |||||||
| chrX:13616790 | C | T | 1 | a0004c0020t0001g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.779-940C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616790 | |||||||
| chrX:13616859 | A | AT | 60 | a0001c0001t0001g0118 a0001c0001t0001g0174 a0001c0001t0001g0199 others(57): Show |
62 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.779-850dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616859 | ||||||
| chrX:13616859 | A | ATT | 19 | a0001c0001t0001g0219 a0001c0001t0002g0070 a0001c0001t0002g0076 others(16): Show |
20 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.779-851_779-850dup others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13616859 | ||||||
| chrX:13616956 | G | A | 1 | a0008c0015t0007g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.779-774G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13616956 | |||||||
| chrX:13617024 | C | T | 64 | a0001c0001t0001g0060 a0001c0001t0001g0219 a0001c0001t0002g0098 others(61): Show |
66 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.779-706C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13617024 | |||||||
| chrX:13617053 | TAG | T | 84 | a0001c0001t0001g0060 a0001c0001t0001g0219 a0001c0001t0002g0098 others(81): Show |
87 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.779-671_779-670del others(2): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617053 | ||||||
| chrX:13617171 | G | C | 5 | a0001c0001t0001g0219 a0001c0001t0003g0094 a0001c0004t0004g0059 others(2): Show |
5 | HG02572.hp1 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.779-559G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13617171 | |||||||
| chrX:13617448 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.779-282G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | chrX | 13617448 | |||||||
| chrX:13617590 | TATC | T | 80 | a0001c0001t0001g0060 a0001c0001t0001g0219 a0001c0001t0002g0098 others(77): Show |
83 | HG00544.hp1 HG00621.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.779-135_779-133del others(3): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chrX | 13617590 | ||||||
| chrX:13618227 | C | T | 5 | a0001c0004t0001g0069 a0001c0004t0001g0196 a0001c0004t0001g0238 others(2): Show |
6 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.1102+174C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618227 | |||||||
| chrX:13618406 | G | T | 1 | a0005c0013t0004g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1102+353G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618406 | |||||||
| chrX:13618524 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1102+471G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618524 | |||||||
| chrX:13618832 | G | T | 1 | a0001c0001t0001g0222 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1103-331G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618832 | |||||||
| chrX:13618864 | T | C | 1 | a0002c0003t0004g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1103-299T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618864 | |||||||
| chrX:13618889 | GA | G | 216 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(213): Show |
222 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1103-263delA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chrX | 13618889 | ||||||
| chrX:13618993 | G | A | 1 | a0010c0011t0004g0058 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1103-170G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13618993 | |||||||
| chrX:13619000 | G | T | 1 | a0001c0001t0002g0070 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1103-163G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 8/11 | chrX | 13619000 | |||||||
| chrX:13619308 | T | C | 1 | a0001c0001t0002g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1183+65T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619308 | |||||||
| chrX:13619463 | G | A | 2 | a0001c0001t0002g0141 a0001c0001t0002g0154 |
2 | NA18989.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1183+220G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619463 | |||||||
| chrX:13619580 | T | G | 2 | a0001c0001t0005g0050 a0001c0001t0005g0051 |
2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1183+337T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619580 | |||||||
| chrX:13619615 | G | A | 15 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0076 others(12): Show |
16 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1183+372G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619615 | |||||||
| chrX:13619666 | T | C | 1 | a0001c0001t0002g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1183+423T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619666 | |||||||
| chrX:13619751 | G | T | 1 | a0005c0013t0004g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1183+508G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619751 | |||||||
| chrX:13619759 | A | G | 10 | a0001c0001t0002g0131 a0001c0001t0002g0137 a0001c0001t0002g0150 others(7): Show |
11 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1183+516A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619759 | |||||||
| chrX:13619815 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1183+572G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13619815 | |||||||
| chrX:13620017 | C | T | 78 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0278 others(75): Show |
82 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(79): Show |
intron_variant | MODIFIER | c.1183+774C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620017 | |||||||
| chrX:13620130 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1183+887C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620130 | |||||||
| chrX:13620173 | T | C | 1 | a0001c0008t0001g0040 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1183+930T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620173 | |||||||
| chrX:13620324 | CACTTACC others(58): Show |
C | 1 | a0001c0001t0001g0041 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1183+1126_1183+119 others(69): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13620324 | ||||||
| chrX:13620434 | G | A | 1 | a0001c0001t0008g0295 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1183+1191G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620434 | |||||||
| chrX:13620475 | T | G | 1 | a0001c0001t0002g0148 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1183+1232T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620475 | |||||||
| chrX:13620511 | C | G | 4 | a0003c0006t0002g0129 a0003c0006t0002g0138 a0003c0006t0004g0291 others(1): Show |
5 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1183+1268C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620511 | |||||||
| chrX:13620517 | C | CA | 5 | a0001c0005t0002g0127 a0003c0006t0002g0129 a0003c0006t0002g0138 others(2): Show |
6 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.1183+1283dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13620517 | ||||||
| chrX:13620670 | C | T | 1 | a0001c0001t0002g0076 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1183+1427C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620670 | |||||||
| chrX:13620797 | A | G | 1 | a0011c0019t0001g0226 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1183+1554A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620797 | |||||||
| chrX:13620918 | C | G | 1 | a0001c0008t0001g0056 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1183+1675C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13620918 | |||||||
| chrX:13621127 | G | A | 4 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0001t0001g0205 others(1): Show |
4 | HG00408.hp1 HG00544.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1183+1884G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621127 | |||||||
| chrX:13621201 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1183+1958C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621201 | |||||||
| chrX:13621331 | T | C | 1 | a0001c0005t0001g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1183+2088T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621331 | |||||||
| chrX:13621717 | G | C | 1 | a0005c0013t0004g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1184-2107G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621717 | |||||||
| chrX:13621791 | A | G | 1 | a0001c0001t0002g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1184-2033A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621791 | |||||||
| chrX:13621956 | A | G | 1 | a0001c0001t0001g0216 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1184-1868A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13621956 | |||||||
| chrX:13622211 | AGAAAG | A | 48 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0076 others(45): Show |
50 | HG00621.hp1 HG00735.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.1184-1607_1184-160 others(9): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13622211 | ||||||
| chrX:13622271 | G | A | 2 | a0004c0021t0001g0042 a0009c0023t0001g0046 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1184-1553G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622271 | |||||||
| chrX:13622284 | G | A | 3 | a0003c0006t0002g0138 a0003c0006t0004g0291 a0003c0006t0006g0005 |
4 | HG01975.hp1 HG02148.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184-1540G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622284 | |||||||
| chrX:13622348 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1184-1476A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622348 | |||||||
| chrX:13622669 | A | G | 218 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(215): Show |
224 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.1184-1155A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622669 | |||||||
| chrX:13622756 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0002g0027 |
2 | HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1184-1068G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622756 | |||||||
| chrX:13622913 | G | C | 1 | a0002c0003t0004g0037 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1184-911G>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13622913 | |||||||
| chrX:13623336 | AT | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0171 a0001c0001t0002g0113 others(3): Show |
6 | HG01169.hp1 HG01256.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184-474delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623336 | ||||||
| chrX:13623339 | T | A | 213 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(210): Show |
219 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1184-485T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623339 | |||||||
| chrX:13623340 | T | A | 2 | a0001c0001t0002g0113 a0001c0001t0003g0079 |
2 | NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1184-484T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623340 | |||||||
| chrX:13623349 | T | A | 1 | a0005c0013t0004g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1184-475T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623349 | |||||||
| chrX:13623350 | T | A | 17 | a0001c0001t0001g0198 a0001c0001t0002g0152 a0001c0001t0002g0153 others(14): Show |
18 | HG01070.hp1 HG01074.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1184-474T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623350 | |||||||
| chrX:13623351 | A | T | 4 | a0003c0006t0002g0129 a0003c0006t0002g0138 a0003c0006t0004g0291 others(1): Show |
5 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184-473A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623351 | |||||||
| chrX:13623376 | G | GTTTTTTT others(2): Show |
4 | a0003c0006t0002g0129 a0003c0006t0002g0138 a0003c0006t0004g0291 others(1): Show |
5 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184-448_1184-447i others(11): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623376 | |||||||
| chrX:13623377 | G | GT | 18 | a0001c0001t0001g0072 a0001c0001t0001g0200 a0001c0001t0001g0205 others(15): Show |
18 | HG00408.hp1 HG02071.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1184-427dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(3): Show |
1 | a0001c0001t0004g0271 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1184-436_1184-427d others(12): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(4): Show |
1 | a0002c0003t0004g0159 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1184-437_1184-427d others(13): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(5): Show |
1 | a0005c0013t0004g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1184-438_1184-427d others(14): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(6): Show |
21 | a0001c0001t0005g0050 a0001c0008t0001g0040 a0002c0002t0004g0017 others(18): Show |
23 | HG01109.hp1 HG01243.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1184-439_1184-427d others(15): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(7): Show |
20 | a0001c0001t0003g0087 a0001c0001t0004g0025 a0001c0001t0005g0051 others(17): Show |
20 | HG00621.hp1 HG01070.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1184-440_1184-427d others(16): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(8): Show |
4 | a0002c0003t0004g0234 a0002c0003t0005g0053 a0002c0003t0007g0011 others(1): Show |
4 | HG02280.hp2 HG02451.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184-441_1184-427d others(17): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(9): Show |
1 | a0002c0003t0005g0048 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1184-442_1184-427d others(18): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(10): Show |
3 | a0001c0001t0002g0076 a0001c0001t0003g0273 a0001c0007t0001g0274 |
3 | HG00280.hp1 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1184-443_1184-427d others(19): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(11): Show |
24 | a0001c0001t0001g0140 a0001c0001t0001g0221 a0001c0001t0001g0222 others(21): Show |
24 | HG00099.hp2 HG00408.hp2 HG01943.hp1 others(21): Show |
intron_variant | MODIFIER | c.1184-444_1184-427d others(20): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(12): Show |
57 | a0001c0001t0001g0062 a0001c0001t0001g0084 a0001c0001t0001g0116 others(54): Show |
58 | HG00597.hp1 HG00639.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.1184-445_1184-427d others(21): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(13): Show |
42 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0118 others(39): Show |
44 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.1184-446_1184-427d others(22): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(14): Show |
13 | a0001c0001t0001g0041 a0001c0001t0001g0060 a0001c0001t0001g0180 others(10): Show |
13 | HG01346.hp1 HG02074.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184-427_1184-426i others(23): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(15): Show |
5 | a0001c0001t0001g0232 a0001c0001t0001g0255 a0001c0001t0002g0098 others(2): Show |
5 | HG01358.hp1 HG01891.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184-427_1184-426i others(24): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | GTTTTTTT others(17): Show |
1 | a0001c0001t0002g0153 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1184-427_1184-426i others(26): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chrX | 13623377 | ||||||
| chrX:13623377 | G | T | 4 | a0003c0006t0002g0129 a0003c0006t0002g0138 a0003c0006t0004g0291 others(1): Show |
5 | HG01975.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184-447G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623377 | |||||||
| chrX:13623438 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0248 a0001c0001t0003g0100 |
3 | HG02602.hp1 HG03490.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1184-386G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623438 | |||||||
| chrX:13623467 | C | T | 29 | a0002c0002t0004g0009 a0002c0002t0004g0017 a0002c0002t0004g0021 others(26): Show |
30 | HG00621.hp1 HG02155.hp2 HG02451.hp1 others(27): Show |
intron_variant | MODIFIER | c.1184-357C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623467 | |||||||
| chrX:13623657 | C | A | 139 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(136): Show |
141 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.1184-167C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623657 | |||||||
| chrX:13623712 | T | C | 1 | a0001c0001t0003g0168 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1184-112T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623712 | |||||||
| chrX:13623812 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1184-12T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 9/11 | chrX | 13623812 | |||||||
| chrX:13623959 | A | G | 1 | a0001c0001t0009g0214 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1285+34A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13623959 | |||||||
| chrX:13624158 | C | T | 3 | a0001c0001t0001g0161 a0005c0013t0004g0029 a0007c0016t0004g0026 |
3 | HG01109.hp1 HG02109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1285+233C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624158 | |||||||
| chrX:13624246 | A | G | 9 | a0001c0001t0001g0060 a0001c0001t0008g0295 a0001c0005t0001g0055 others(6): Show |
9 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1285+321A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624246 | |||||||
| chrX:13624528 | C | T | 195 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(192): Show |
199 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.1285+603C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624528 | |||||||
| chrX:13624653 | T | A | 216 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(213): Show |
222 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1285+728T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624653 | |||||||
| chrX:13624680 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1285+755G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624680 | |||||||
| chrX:13624773 | C | T | 3 | a0001c0001t0004g0223 a0001c0001t0004g0247 a0001c0004t0004g0059 |
3 | HG01070.hp2 HG01071.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1285+848C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624773 | |||||||
| chrX:13624924 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0003g0130 |
2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1285+999G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624924 | |||||||
| chrX:13624953 | A | G | 6 | a0002c0003t0004g0002 a0002c0003t0004g0159 a0002c0003t0004g0164 others(3): Show |
7 | HG01074.hp1 HG01243.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1285+1028A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624953 | |||||||
| chrX:13624963 | A | T | 2 | a0001c0001t0005g0050 a0001c0001t0005g0051 |
2 | HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1285+1038A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624963 | |||||||
| chrX:13624990 | A | T | 14 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0076 others(11): Show |
15 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1285+1065A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13624990 | |||||||
| chrX:13625103 | G | A | 3 | a0003c0006t0002g0129 a0003c0006t0004g0291 a0003c0006t0006g0005 |
4 | HG02004.hp1 HG02148.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1285+1178G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625103 | |||||||
| chrX:13625154 | TACAA | T | 5 | a0004c0010t0001g0236 a0004c0010t0003g0090 a0004c0020t0001g0047 others(2): Show |
5 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1285+1233_1285+123 others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625154 | ||||||
| chrX:13625204 | T | C | 1 | a0001c0007t0003g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1285+1279T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625204 | |||||||
| chrX:13625227 | C | A | 139 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(136): Show |
141 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.1285+1302C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625227 | |||||||
| chrX:13625352 | C | T | 149 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(146): Show |
151 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.1285+1427C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625352 | |||||||
| chrX:13625410 | T | A | 1 | a0001c0001t0002g0120 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1285+1485T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625410 | |||||||
| chrX:13625536 | T | C | 1 | a0001c0004t0004g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1286-1475T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625536 | |||||||
| chrX:13625537 | A | G | 2 | a0001c0001t0001g0278 a0001c0001t0004g0271 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1286-1474A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625537 | |||||||
| chrX:13625641 | A | T | 3 | a0003c0006t0002g0129 a0003c0006t0004g0291 a0003c0006t0006g0005 |
4 | HG02004.hp1 HG02148.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286-1370A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625641 | |||||||
| chrX:13625643 | T | C | 2 | a0001c0001t0002g0141 a0001c0001t0002g0154 |
2 | NA18989.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1286-1368T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625643 | |||||||
| chrX:13625662 | C | T | 3 | a0003c0006t0002g0129 a0003c0006t0004g0291 a0003c0006t0006g0005 |
4 | HG02004.hp1 HG02148.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.1286-1349C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625662 | |||||||
| chrX:13625828 | A | G | 216 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(213): Show |
222 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.1286-1183A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625828 | |||||||
| chrX:13625864 | T | C | 1 | a0007c0016t0004g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1286-1147T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13625864 | |||||||
| chrX:13625885 | C | CA | 11 | a0001c0001t0001g0199 a0001c0001t0001g0218 a0001c0001t0001g0249 others(8): Show |
11 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1286-1108dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | ||||||
| chrX:13625885 | C | CAA | 8 | a0002c0002t0004g0215 a0002c0002t0005g0080 a0002c0003t0004g0037 others(5): Show |
9 | HG02004.hp1 HG02148.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1286-1109_1286-110 others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | ||||||
| chrX:13625885 | C | CAAA | 36 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0076 others(33): Show |
38 | HG00621.hp1 HG00735.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1286-1110_1286-110 others(7): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | ||||||
| chrX:13625885 | C | CAAAA | 9 | a0001c0001t0002g0163 a0001c0001t0004g0223 a0001c0001t0004g0247 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1286-1111_1286-110 others(8): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | ||||||
| chrX:13625885 | C | CAAAAAAA | 8 | a0001c0001t0001g0008 a0001c0001t0001g0161 a0001c0001t0001g0245 others(5): Show |
8 | HG02109.hp2 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286-1114_1286-110 others(11): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625885 | ||||||
| chrX:13625895 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0002g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1286-1108_1286-109 others(19): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625895 | ||||||
| chrX:13625896 | AAAAAAAA others(7): Show |
A | 139 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(136): Show |
141 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1286-1102_1286-108 others(18): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625896 | ||||||
| chrX:13625897 | AAAAAAAG others(6): Show |
A | 7 | a0001c0001t0003g0273 a0002c0003t0004g0002 a0002c0003t0004g0159 others(4): Show |
8 | HG00280.hp1 HG01074.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286-1107_1286-109 others(17): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13625897 | ||||||
| chrX:13626223 | C | G | 6 | a0001c0008t0001g0056 a0002c0003t0004g0031 a0002c0003t0004g0032 others(3): Show |
6 | HG01070.hp1 HG01891.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.1286-788C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13626223 | |||||||
| chrX:13626394 | G | A | 1 | a0002c0003t0006g0043 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1286-617G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13626394 | |||||||
| chrX:13626676 | A | G | 43 | a0001c0001t0001g0142 a0001c0001t0002g0027 a0001c0001t0004g0025 others(40): Show |
45 | HG00621.hp1 HG01070.hp2 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.1286-335A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13626676 | |||||||
| chrX:13626752 | T | TCTTTGTG others(4): Show |
1 | a0001c0018t0002g0067 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1286-246_1286-236d others(13): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chrX | 13626752 | ||||||
| chrX:13626773 | T | C | 1 | a0001c0001t0002g0068 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1286-238T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13626773 | |||||||
| chrX:13626879 | G | T | 40 | a0001c0001t0001g0142 a0001c0001t0002g0027 a0001c0001t0004g0025 others(37): Show |
41 | HG00621.hp1 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1286-132G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 10/11 | chrX | 13626879 | |||||||
| chrX:13627413 | C | T | 1 | a0001c0001t0008g0012 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1551+137C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627413 | |||||||
| chrX:13627530 | C | A | 1 | a0001c0001t0003g0093 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1551+254C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627530 | |||||||
| chrX:13627544 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1551+268C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627544 | |||||||
| chrX:13627550 | A | G | 2 | a0004c0010t0001g0236 a0004c0010t0003g0090 |
2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1551+274A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627550 | |||||||
| chrX:13627663 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1551+387C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627663 | |||||||
| chrX:13627781 | T | C | 6 | a0001c0008t0001g0056 a0002c0003t0004g0284 a0002c0003t0004g0285 others(3): Show |
7 | HG02004.hp1 HG02109.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1551+505T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627781 | |||||||
| chrX:13627923 | A | C | 2 | a0005c0013t0004g0029 a0007c0016t0004g0026 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1551+647A>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13627923 | |||||||
| chrX:13628060 | A | G | 6 | a0001c0001t0001g0278 a0004c0010t0001g0236 a0004c0010t0003g0090 others(3): Show |
6 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1551+784A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628060 | |||||||
| chrX:13628135 | C | G | 2 | a0003c0006t0004g0291 a0003c0006t0006g0005 |
3 | HG02148.hp2 NA18959.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1551+859C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628135 | |||||||
| chrX:13628475 | A | G | 40 | a0001c0001t0001g0142 a0001c0001t0002g0027 a0001c0001t0004g0025 others(37): Show |
41 | HG00621.hp1 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.1551+1199A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628475 | |||||||
| chrX:13628552 | G | A | 8 | a0002c0002t0004g0009 a0002c0002t0004g0017 a0002c0002t0004g0021 others(5): Show |
9 | NA18939.hp2 NA18944.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.1551+1276G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628552 | |||||||
| chrX:13628607 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1551+1331A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628607 | |||||||
| chrX:13628641 | C | A | 4 | a0001c0005t0001g0225 a0001c0005t0001g0244 a0001c0005t0001g0272 others(1): Show |
4 | HG03041.hp1 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1551+1365C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628641 | |||||||
| chrX:13628731 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1551+1455C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628731 | |||||||
| chrX:13628761 | C | T | 2 | a0005c0013t0004g0029 a0007c0016t0004g0026 |
2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1551+1485C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628761 | |||||||
| chrX:13628807 | C | CA | 5 | a0001c0001t0001g0084 a0001c0001t0001g0190 a0001c0001t0002g0044 others(2): Show |
5 | HG01928.hp1 HG02738.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1551+1539dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13628807 | ||||||
| chrX:13628815 | AC | A | 79 | a0001c0001t0001g0142 a0001c0001t0001g0221 a0001c0001t0001g0222 others(76): Show |
83 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.1551+1543delC | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13628815 | ||||||
| chrX:13628816 | C | A | 207 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(204): Show |
209 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1551+1540C>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628816 | |||||||
| chrX:13628851 | G | T | 11 | a0002c0003t0004g0002 a0002c0003t0004g0031 a0002c0003t0004g0032 others(8): Show |
12 | HG01070.hp1 HG01074.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1551+1575G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628851 | |||||||
| chrX:13628893 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0002g0027 |
2 | HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1551+1617A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13628893 | |||||||
| chrX:13629114 | T | C | 1 | a0001c0001t0003g0087 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1551+1838T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629114 | |||||||
| chrX:13629387 | T | C | 74 | a0001c0001t0001g0006 a0001c0001t0001g0062 a0001c0001t0001g0084 others(71): Show |
75 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1551+2111T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629387 | |||||||
| chrX:13629501 | T | C | 35 | a0001c0001t0005g0050 a0001c0001t0005g0051 a0002c0002t0004g0009 others(32): Show |
37 | HG00621.hp1 HG01109.hp1 HG02148.hp2 others(34): Show |
intron_variant | MODIFIER | c.1551+2225T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629501 | |||||||
| chrX:13629571 | G | A | 3 | a0001c0001t0002g0125 a0001c0001t0002g0165 a0001c0001t0003g0023 |
3 | NA18954.hp1 NA18956.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1551+2295G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629571 | |||||||
| chrX:13629695 | T | G | 70 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0076 others(67): Show |
74 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.1551+2419T>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629695 | |||||||
| chrX:13629801 | G | T | 2 | a0001c0001t0002g0075 a0001c0001t0003g0087 |
2 | HG02683.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1551+2525G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629801 | |||||||
| chrX:13629930 | C | T | 3 | a0002c0003t0004g0284 a0002c0003t0004g0285 a0007c0016t0004g0026 |
3 | HG01109.hp1 HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1551+2654C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629930 | |||||||
| chrX:13629950 | A | G | 5 | a0001c0001t0004g0025 a0001c0001t0004g0223 a0001c0001t0004g0247 others(2): Show |
5 | HG01070.hp2 HG01071.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1551+2674A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13629950 | |||||||
| chrX:13630077 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1551+2801A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630077 | |||||||
| chrX:13630291 | G | A | 57 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0076 others(54): Show |
60 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1552-2694G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630291 | |||||||
| chrX:13630296 | A | G | 57 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0076 others(54): Show |
60 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.1552-2689A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630296 | |||||||
| chrX:13630429 | T | C | 1 | a0001c0001t0002g0147 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1552-2556T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630429 | |||||||
| chrX:13630442 | C | G | 3 | a0002c0003t0004g0032 a0002c0003t0004g0033 a0002c0003t0004g0169 |
3 | HG01891.hp1 HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1552-2543C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630442 | |||||||
| chrX:13630611 | G | A | 1 | a0001c0001t0004g0271 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1552-2374G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630611 | |||||||
| chrX:13630736 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1552-2249C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630736 | |||||||
| chrX:13630737 | T | C | 76 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0278 others(73): Show |
80 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(77): Show |
intron_variant | MODIFIER | c.1552-2248T>C | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13630737 | |||||||
| chrX:13631029 | CAT | C | 45 | a0002c0002t0004g0009 a0002c0002t0004g0017 a0002c0002t0004g0021 others(42): Show |
47 | HG00621.hp1 HG01070.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.1552-1955_1552-195 others(6): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13631029 | |||||||
| chrX:13631217 | T | A | 70 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0076 others(67): Show |
74 | HG00621.hp1 HG00735.hp2 HG01070.hp1 others(71): Show |
intron_variant | MODIFIER | c.1552-1768T>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13631217 | |||||||
| chrX:13631470 | A | T | 6 | a0002c0003t0004g0031 a0002c0003t0004g0158 a0002c0003t0004g0164 others(3): Show |
7 | HG01070.hp1 HG02004.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1552-1515A>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13631470 | |||||||
| chrX:13631503 | C | T | 40 | a0002c0002t0004g0009 a0002c0002t0004g0017 a0002c0002t0004g0021 others(37): Show |
42 | HG00621.hp1 HG01070.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1552-1482C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13631503 | |||||||
| chrX:13631504 | G | A | 9 | a0001c0001t0004g0025 a0001c0001t0004g0223 a0001c0001t0004g0247 others(6): Show |
9 | HG01070.hp2 HG01071.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1552-1481G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13631504 | |||||||
| chrX:13631815 | TAAAAC | T | 4 | a0002c0003t0004g0284 a0002c0003t0004g0285 a0002c0003t0006g0043 others(1): Show |
4 | HG01109.hp1 HG02109.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1552-1165_1552-116 others(9): Show |
EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13631815 | ||||||
| chrX:13632019 | G | T | 1 | a0002c0002t0006g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1552-966G>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632019 | |||||||
| chrX:13632162 | C | G | 139 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0041 others(136): Show |
141 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.1552-823C>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632162 | |||||||
| chrX:13632169 | C | T | 1 | a0002c0002t0006g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1552-816C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632169 | |||||||
| chrX:13632215 | C | CA | 11 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0002g0076 others(8): Show |
12 | HG00735.hp2 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1552-759dupA | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13632215 | ||||||
| chrX:13632297 | G | GT | 72 | a0001c0001t0001g0024 a0001c0001t0001g0072 a0001c0001t0001g0084 others(69): Show |
72 | HG00544.hp1 HG00621.hp1 HG01175.hp2 others(69): Show |
intron_variant | MODIFIER | c.1552-666dupT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13632297 | ||||||
| chrX:13632297 | GT | G | 25 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0278 others(22): Show |
26 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.1552-666delT | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chrX | 13632297 | ||||||
| chrX:13632333 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1552-652A>G | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632333 | |||||||
| chrX:13632341 | G | A | 6 | a0002c0003t0004g0234 a0002c0003t0005g0048 a0002c0003t0005g0052 others(3): Show |
6 | HG02451.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1552-644G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632341 | |||||||
| chrX:13632403 | G | A | 1 | a0011c0019t0001g0226 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1552-582G>A | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632403 | |||||||
| chrX:13632549 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1552-436C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632549 | |||||||
| chrX:13632824 | C | T | 1 | a0001c0001t0002g0114 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1552-161C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632824 | |||||||
| chrX:13632901 | C | T | 4 | a0002c0003t0004g0284 a0002c0003t0004g0285 a0002c0003t0006g0043 others(1): Show |
4 | HG01109.hp1 HG02109.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1552-84C>T | EGFL6 | ENSG00000198759.12 | transcript | ENST00000361306.6 | protein_coding | 11/11 | chrX | 13632901 |