Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51162 |
| ensemblid | ENSG00000172889.16 |
| hgncid | 20594 |
| symbol | EGFL7 |
| name | EGF like domain multiple 7 |
| refseq_nuc | NM_016215.5 |
| refseq_prot | NP_057299.1 |
| ensembl_nuc | ENST00000308874.12 |
| ensembl_prot | ENSP00000307843.7 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 136662916 |
| end | 136672678 |
| strand | + |
| ver | v1.2 |
| region | chr9:136662916-136672678 |
| region5000 | chr9:136657916-136677678 |
| regionname0 | EGFL7_chr9_136662916_136672678 |
| regionname5000 | EGFL7_chr9_136657916_136677678 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 273 | 353 | 79 | 61 | 160 | 11 | 40 | 119 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| a0002 | 0/0 | 273 | 67 | 18 | 16 | 25 | 3 | 5 | 20 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| a0003 | 0/0 | 273 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| a0004 | 0/0 | 273 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| a0005 | 0/0 | 273 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| a0006 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| a0007 | 0/0 | 273 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| a0008 | 0/0 | 273 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| a0009 | 0/0 | 273 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| a0010 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| a0011 | 0/0 | 273 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | MRGSQ others(268): Show |
chr9 | 136657916 | 136677678 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 819 | 346 | 74 | 60 | 159 | 11 | 40 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0001c0003 | 0/0 | 819 | 3 | 3 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0001c0007 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0001c0013 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0001c0014 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0001c0015 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0002c0002 | 0/0 | 819 | 67 | 18 | 16 | 25 | 3 | 5 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0003c0006 | 0/0 | 819 | 2 | 0 | 0 | 0 | 2 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0004c0005 | 0/0 | 819 | 2 | 0 | 0 | 1 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0005c0004 | 0/0 | 819 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0006c0008 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0007c0010 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0008c0012 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0009c0009 | 0/0 | 819 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0010c0016 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 | ||
| a0011c0011 | 0/0 | 819 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | ATGAG others(814): Show |
chr9 | 136657916 | 136677678 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1759 | 288 | 55 | 38 | 152 | 10 | 32 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0002 | 0/0 | 1759 | 3 | 0 | 2 | 0 | 1 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0003 | 1/0 | 1759 | 10 | 9 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0004 | 0/0 | 1759 | 2 | 0 | 1 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0005 | 0/0 | 1759 | 12 | 2 | 7 | 0 | 0 | 3 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0006 | 0/0 | 1759 | 7 | 2 | 1 | 4 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0007 | 0/0 | 1759 | 8 | 0 | 4 | 0 | 0 | 4 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0008 | 0/0 | 1759 | 6 | 1 | 5 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0010 | 0/0 | 1759 | 2 | 1 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0012 | 0/0 | 1759 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0013 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0015 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0016 | 0/0 | 1759 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0017 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0018 | 0/0 | 1774 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1769): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0019 | 0/0 | 1759 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0001t0020 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0003t0001 | 0/0 | 1759 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0003t0003 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0007t0001 | 0/0 | 1759 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0013t0001 | 0/0 | 1759 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0014t0001 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0001c0015t0014 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0002c0002t0001 | 0/0 | 1759 | 22 | 1 | 6 | 13 | 0 | 2 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0002c0002t0002 | 0/0 | 1759 | 19 | 4 | 9 | 4 | 1 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0002c0002t0003 | 0/0 | 1759 | 6 | 3 | 0 | 1 | 1 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0002c0002t0004 | 0/0 | 1759 | 12 | 3 | 0 | 7 | 1 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0002c0002t0006 | 0/0 | 1759 | 4 | 4 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0002c0002t0008 | 0/0 | 1759 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0002c0002t0009 | 0/0 | 1759 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0002c0002t0011 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0003c0006t0002 | 0/0 | 1759 | 2 | 0 | 0 | 0 | 2 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0004c0005t0001 | 0/0 | 1759 | 2 | 0 | 0 | 1 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0005c0004t0006 | 0/0 | 1759 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0006c0008t0001 | 0/0 | 1759 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0007c0010t0001 | 0/0 | 1759 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0008c0012t0001 | 0/0 | 1759 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0009c0009t0001 | 0/0 | 1759 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0010c0016t0001 | 0/0 | 1759 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| a0011c0011t0005 | 0/0 | 1759 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | GGAGC others(1754): Show |
chr9 | 136657916 | 136677678 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 40 | 2 | 10 | 18 | 1 | 8 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0002 | 0/0 | 46 | 3 | 7 | 32 | 2 | 2 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0003 | 0/0 | 15 | 0 | 4 | 9 | 0 | 2 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0004 | 0/0 | 16 | 0 | 5 | 1 | 3 | 7 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0006 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0007 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0009 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0015 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0016 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0019 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0022 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0023 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0003g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0003g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0005g0001 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0005g0018 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0005g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0006g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0006g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0006g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0007g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0007g0003 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0007g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0008g0001 | 0/0 | 6 | 1 | 5 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0010g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0010g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0012g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0015g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0016g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0017g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0018g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0019g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0001t0020g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0003t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0007t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0013t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0014t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0001c0015t0014g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0005 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0014 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0002g0005 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0002g0011 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0004g0005 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0008g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0009g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0002c0002t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0003c0006t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0004c0005t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0004c0005t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0005c0004t0006g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0006c0008t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0007c0010t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0008c0012t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0009c0009t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0010c0016t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| a0011c0011t0005g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0011 | EUR | GBR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00438 | hp2 | a0002 | c0002 | t0004 | g0005 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00558 | hp1 | a0006 | c0008 | t0001 | g0003 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0020 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00639 | hp1 | a0007 | c0010 | t0001 | g0004 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0114 | EAS | CHS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0002 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0073 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0133 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01069 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0107 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01099 | hp1 | a0001 | c0001 | t0012 | g0013 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0066 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01168 | hp2 | a0008 | c0012 | t0001 | g0002 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0119 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0030 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01258 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01358 | hp2 | a0002 | c0002 | t0008 | g0011 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01515 | hp1 | a0003 | c0006 | t0002 | g0005 | EUR | IBS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01516 | hp1 | a0002 | c0002 | t0004 | g0035 | EUR | IBS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01517 | hp2 | a0003 | c0006 | t0002 | g0005 | EUR | IBS | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0134 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0013 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01993 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02004 | hp1 | a0009 | c0009 | t0001 | g0004 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02080 | hp2 | a0004 | c0005 | t0001 | g0038 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02135 | hp2 | a0001 | c0001 | t0016 | g0065 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02145 | hp1 | a0001 | c0015 | t0014 | g0141 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02148 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02148 | hp2 | a0001 | c0013 | t0001 | g0002 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02258 | hp2 | a0001 | c0003 | t0003 | g0146 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02293 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02300 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02615 | hp1 | a0001 | c0001 | t0017 | g0010 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0131 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02630 | hp2 | a0001 | c0014 | t0001 | g0021 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02698 | hp1 | a0001 | c0001 | t0007 | g0140 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0018 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02818 | hp1 | a0002 | c0002 | t0006 | g0088 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0094 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02886 | hp2 | a0002 | c0002 | t0004 | g0060 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02922 | hp1 | a0002 | c0002 | t0009 | g0037 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0144 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02976 | hp1 | a0005 | c0004 | t0006 | g0010 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03017 | hp1 | a0001 | c0001 | t0019 | g0070 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03098 | hp1 | a0005 | c0004 | t0006 | g0010 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03130 | hp1 | a0002 | c0002 | t0004 | g0089 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03130 | hp2 | a0002 | c0002 | t0011 | g0017 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03139 | hp1 | a0002 | c0002 | t0004 | g0061 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0017 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0143 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0003 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03492 | hp2 | a0001 | c0001 | t0007 | g0003 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0017 | AFR | ESN | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03579 | hp2 | a0002 | c0002 | t0006 | g0086 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0082 | SAS | STU | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03927 | hp1 | a0004 | c0005 | t0001 | g0003 | SAS | BEB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | BEB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0003 | SAS | BEB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0011 | SAS | STU | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | STU | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | CHB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0044 | AFR | YRI | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18941 | hp1 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18948 | hp1 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18948 | hp2 | a0001 | c0001 | t0018 | g0121 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18951 | hp1 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18966 | hp1 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18970 | hp2 | a0002 | c0002 | t0004 | g0017 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0020 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18997 | hp1 | a0010 | c0016 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | LWK | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19043 | hp1 | a0001 | c0001 | t0020 | g0046 | AFR | LWK | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19065 | hp1 | a0002 | c0002 | t0004 | g0044 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19072 | hp2 | a0001 | c0007 | t0001 | g0048 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19080 | hp2 | a0002 | c0002 | t0003 | g0005 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19086 | hp1 | a0002 | c0002 | t0004 | g0005 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19090 | hp2 | a0002 | c0002 | t0004 | g0062 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ASW | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | TSI | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA20805 | hp1 | a0002 | c0002 | t0003 | g0081 | EUR | TSI | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA20905 | hp2 | a0002 | c0002 | t0004 | g0005 | SAS | GIH | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0030 | AMR | CLM | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG03471 | hp2 | a0001 | c0001 | t0013 | g0029 | AFR | MSL | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG06807 | hp1 | a0002 | c0002 | t0009 | g0037 | AFR | USA | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| HG06807 | hp2 | a0002 | c0002 | t0006 | g0087 | AFR | USA | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA20300 | hp1 | a0002 | c0002 | t0003 | g0080 | AFR | USA | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| NA21309 | hp2 | a0011 | c0011 | t0005 | g0002 | AFR | LWK | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0033 | REF | REF | EGFL7_chr9_136657916_136677678 | EGFL7 | chr9 | 136657916 | 136677678 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136668639 | A | T | 1 | a0010 | 1 | NA18997.hp1 | missense_variant | MODERATE | c.163A>T | p.Thr55Ser | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/11 | 708/1759 | 163/822 | 55/273 | chr9 | 136668639 | |||
| chr9:136668655 | G | A | 1 | a0006 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.179G>A | p.Arg60Gln | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/11 | 724/1759 | 179/822 | 60/273 | chr9 | 136668655 | |||
| chr9:136669618 | G | C | 1 | a0009 | 1 | HG02004.hp1 | missense_variant | MODERATE | c.210G>C | p.Arg70Ser | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 6/11 | 755/1759 | 210/822 | 70/273 | chr9 | 136669618 | |||
| chr9:136669935 | G | A | 1 | a0007 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.335G>A | p.Arg112Gln | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 7/11 | 880/1759 | 335/822 | 112/273 | chr9 | 136669935 | |||
| chr9:136669940 | G | A | 1 | a0005 | 2 | HG02976.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.340G>A | p.Gly114Arg | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 7/11 | 885/1759 | 340/822 | 114/273 | chr9 | 136669940 | |||
| chr9:136669971 | G | A | 1 | a0011 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.371G>A | p.Arg124His | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 7/11 | 916/1759 | 371/822 | 124/273 | chr9 | 136669971 | |||
| chr9:136670177 | G | A | 1 | a0004 | 2 | HG02080.hp2 HG03927.hp1 |
missense_variant | MODERATE | c.418G>A | p.Glu140Lys | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/11 | 963/1759 | 418/822 | 140/273 | chr9 | 136670177 | |||
| chr9:136670216 | G | A | 2 | a0002 a0003 |
69 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(66): Show |
missense_variant | MODERATE | c.457G>A | p.Val153Ile | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/11 | 1002/1759 | 457/822 | 153/273 | chr9 | 136670216 | |||
| chr9:136671999 | G | C | 1 | a0008 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.710G>C | p.Gly237Ala | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 10/11 | 1255/1759 | 710/822 | 237/273 | chr9 | 136671999 | |||
| chr9:136672057 | G | C | 1 | a0003 | 2 | HG01515.hp1 HG01517.hp2 |
missense_variant | MODERATE | c.768G>C | p.Gln256His | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 10/11 | 1313/1759 | 768/822 | 256/273 | chr9 | 136672057 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136668336 | C | A | 1 | a0001c0007 | 1 | NA19072.hp2 | synonymous_variant | LOW | c.54C>A | p.Gly18Gly | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 4/11 | 599/1759 | 54/822 | 18/273 | chr9 | 136668336 | |||
| chr9:136668342 | A | T | 1 | a0001c0007 | 1 | NA19072.hp2 | synonymous_variant | LOW | c.60A>T | p.Thr20Thr | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 4/11 | 605/1759 | 60/822 | 20/273 | chr9 | 136668342 | |||
| chr9:136669654 | C | G | 1 | a0001c0015 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.246C>G | p.Ala82Ala | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 6/11 | 791/1759 | 246/822 | 82/273 | chr9 | 136669654 | |||
| chr9:136670254 | G | A | 1 | a0001c0003 | 3 | HG02258.hp2 HG02451.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.495G>A | p.Glu165Glu | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/11 | 1040/1759 | 495/822 | 165/273 | chr9 | 136670254 | |||
| chr9:136670299 | A | C | 1 | a0001c0014 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.540A>C | p.Gly180Gly | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/11 | 1085/1759 | 540/822 | 180/273 | chr9 | 136670299 | |||
| chr9:136671997 | C | T | 1 | a0001c0013 | 1 | HG02148.hp2 | synonymous_variant | LOW | c.708C>T | p.Pro236Pro | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 10/11 | 1253/1759 | 708/822 | 236/273 | chr9 | 136671997 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136662939 | C | G | 1 | a0001c0001t0020 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-522C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 1/11 | 5344 | chr9 | 136662939 | ||||||
| chr9:136672295 | C | T | 1 | a0001c0001t0019 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 9 | chr9 | 136672295 | ||||||
| chr9:136672326 | C | T | 3 | a0001c0001t0006 a0002c0002t0006 a0005c0004t0006 |
13 | HG00621.hp2 HG01257.hp2 HG02622.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*40C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 40 | chr9 | 136672326 | ||||||
| chr9:136672371 | A | G | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(27): Show |
389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
3_prime_UTR_variant | MODIFIER | c.*85A>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 85 | chr9 | 136672371 | ||||||
| chr9:136672437 | G | A | 6 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(3): Show |
23 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*151G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 151 | chr9 | 136672437 | ||||||
| chr9:136672492 | C | CCCCTGGC others(8): Show |
1 | a0001c0001t0018 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*220_*234dupCACCCT others(9): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 235 | INFO_REALIGN_3_PRIME | chr9 | 136672492 | |||||
| chr9:136672544 | G | A | 6 | a0001c0001t0002 a0001c0001t0004 a0002c0002t0002 others(3): Show |
39 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*258G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 258 | chr9 | 136672544 | ||||||
| chr9:136672593 | T | G | 2 | a0001c0001t0013 a0001c0015t0014 |
2 | HG02145.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*307T>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 307 | chr9 | 136672593 | ||||||
| chr9:136672595 | G | A | 1 | a0001c0001t0015 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*309G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 309 | chr9 | 136672595 | ||||||
| chr9:136672643 | C | G | 1 | a0001c0001t0017 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 357 | chr9 | 136672643 | ||||||
| chr9:136672669 | T | C | 2 | a0001c0001t0007 a0001c0001t0012 |
9 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*383T>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 383 | chr9 | 136672669 | ||||||
| chr9:136672670 | G | A | 1 | a0001c0001t0016 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*384G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 384 | chr9 | 136672670 | ||||||
| chr9:136672674 | C | T | 3 | a0001c0001t0010 a0002c0002t0009 a0002c0002t0011 |
5 | HG01109.hp2 HG02922.hp1 HG03130.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*388C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 11/11 | 388 | chr9 | 136672674 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:136663117 | G | A | 1 | a0001c0001t0020g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-353+9G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 1/10 | chr9 | 136663117 | |||||||
| chr9:136663142 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-353+34C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 1/10 | chr9 | 136663142 | |||||||
| chr9:136663230 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-353+122G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 1/10 | chr9 | 136663230 | |||||||
| chr9:136663313 | A | C | 7 | a0001c0001t0001g0045 a0001c0001t0001g0142 a0001c0001t0010g0143 others(4): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-352-95A>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 1/10 | chr9 | 136663313 | |||||||
| chr9:136663640 | T | A | 1 | a0001c0007t0001g0048 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-137+17T>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136663640 | |||||||
| chr9:136663692 | G | A | 2 | a0001c0001t0001g0142 a0001c0015t0014g0141 |
2 | HG02145.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-137+69G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136663692 | |||||||
| chr9:136663774 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(85): Show |
246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.-137+151C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136663774 | |||||||
| chr9:136664295 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0049 |
3 | HG01074.hp2 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-136-397G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136664295 | |||||||
| chr9:136664297 | C | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0049 |
3 | HG01074.hp2 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-136-395C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136664297 | |||||||
| chr9:136664319 | G | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0015 others(15): Show |
40 | HG01891.hp2 HG02074.hp1 HG02132.hp1 others(37): Show |
intron_variant | MODIFIER | c.-136-373G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136664319 | |||||||
| chr9:136664445 | G | C | 1 | a0002c0002t0004g0060 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-136-247G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136664445 | |||||||
| chr9:136664581 | G | A | 1 | a0002c0002t0004g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-136-111G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136664581 | |||||||
| chr9:136664675 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
278 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.-136-17A>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136664675 | |||||||
| chr9:136664676 | A | T | 1 | a0001c0001t0007g0140 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-136-16A>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136664676 | |||||||
| chr9:136664682 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-136-10C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 2/10 | chr9 | 136664682 | |||||||
| chr9:136664812 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-43+27G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136664812 | |||||||
| chr9:136664831 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0049 |
3 | HG01074.hp2 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-43+46C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136664831 | |||||||
| chr9:136664871 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-43+86C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136664871 | |||||||
| chr9:136665094 | G | A | 2 | a0001c0003t0001g0144 a0001c0003t0001g0145 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-43+309G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665094 | |||||||
| chr9:136665261 | T | C | 2 | a0001c0001t0003g0031 a0001c0001t0005g0030 |
4 | HG01123.hp2 HG01256.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+476T>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665261 | |||||||
| chr9:136665316 | C | T | 2 | a0001c0003t0001g0144 a0001c0003t0001g0145 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-43+531C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665316 | |||||||
| chr9:136665349 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-43+564C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665349 | |||||||
| chr9:136665382 | C | A | 1 | a0002c0002t0004g0062 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-43+597C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665382 | |||||||
| chr9:136665400 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0003t0001g0144 others(2): Show |
6 | HG01106.hp2 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43+615C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665400 | |||||||
| chr9:136665505 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-43+720G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665505 | |||||||
| chr9:136665591 | G | A | 1 | a0002c0002t0001g0063 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-43+806G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665591 | |||||||
| chr9:136665629 | G | A | 2 | a0001c0001t0003g0031 a0001c0001t0005g0030 |
4 | HG01123.hp2 HG01256.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43+844G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665629 | |||||||
| chr9:136665688 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(109): Show |
295 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.-43+903T>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665688 | |||||||
| chr9:136665750 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-43+965G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665750 | |||||||
| chr9:136665775 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-43+990C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665775 | |||||||
| chr9:136665842 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-43+1057G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665842 | |||||||
| chr9:136665869 | G | C | 2 | a0001c0001t0010g0066 a0001c0001t0010g0143 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-43+1084G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665869 | |||||||
| chr9:136665989 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-43+1204C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665989 | |||||||
| chr9:136665995 | G | T | 38 | a0001c0001t0001g0076 a0001c0001t0010g0066 a0001c0001t0010g0143 others(35): Show |
64 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-43+1210G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136665995 | |||||||
| chr9:136666000 | C | A | 1 | a0001c0015t0014g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-43+1215C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666000 | |||||||
| chr9:136666122 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-43+1337G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666122 | |||||||
| chr9:136666177 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-43+1392C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666177 | |||||||
| chr9:136666224 | G | T | 2 | a0001c0001t0010g0066 a0001c0001t0010g0143 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-43+1439G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666224 | |||||||
| chr9:136666250 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-43+1465T>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666250 | |||||||
| chr9:136666382 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
291 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.-43+1597A>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666382 | |||||||
| chr9:136666428 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-43+1643G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666428 | |||||||
| chr9:136666446 | G | A | 4 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0006g0020 others(1): Show |
8 | HG00621.hp2 HG01257.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43+1661G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666446 | |||||||
| chr9:136666447 | C | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0083 a0001c0001t0006g0020 others(1): Show |
8 | HG00621.hp2 HG01257.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.-43+1662C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666447 | |||||||
| chr9:136666484 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG01074.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-43+1699G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666484 | |||||||
| chr9:136666732 | C | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0090 others(18): Show |
42 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.-42-1509C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666732 | |||||||
| chr9:136666736 | C | G | 1 | a0001c0001t0001g0023 | 4 | HG02273.hp2 HG02293.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.-42-1505C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666736 | |||||||
| chr9:136666764 | C | A | 1 | a0001c0007t0001g0048 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-42-1477C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666764 | |||||||
| chr9:136666879 | C | G | 1 | a0001c0001t0005g0030 | 2 | HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.-42-1362C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666879 | |||||||
| chr9:136666910 | G | GC | 6 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(3): Show |
12 | NA18747.hp2 NA18939.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.-42-1324dupC | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 136666910 | ||||||
| chr9:136666998 | C | T | 1 | a0001c0001t0005g0030 | 2 | HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.-42-1243C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136666998 | |||||||
| chr9:136667242 | C | G | 2 | a0002c0002t0003g0081 a0002c0002t0003g0082 |
2 | HG03688.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-42-999C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667242 | |||||||
| chr9:136667253 | C | A | 5 | a0002c0002t0004g0089 a0002c0002t0006g0086 a0002c0002t0006g0087 others(2): Show |
5 | HG02622.hp2 HG02818.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42-988C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667253 | |||||||
| chr9:136667263 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
419 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(416): Show |
intron_variant | MODIFIER | c.-42-978G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667263 | |||||||
| chr9:136667307 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-42-934C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667307 | |||||||
| chr9:136667383 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-42-858G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667383 | |||||||
| chr9:136667407 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG01074.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.-42-834C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667407 | |||||||
| chr9:136667408 | G | A | 1 | a0001c0001t0005g0030 | 2 | HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.-42-833G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667408 | |||||||
| chr9:136667544 | C | T | 3 | a0001c0003t0001g0144 a0001c0003t0001g0145 a0001c0003t0003g0146 |
3 | HG02258.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-42-697C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667544 | |||||||
| chr9:136667622 | A | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG00423.hp1 HG00438.hp1 |
intron_variant | MODIFIER | c.-42-619A>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667622 | |||||||
| chr9:136667696 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(182): Show |
429 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(426): Show |
intron_variant | MODIFIER | c.-42-545T>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667696 | |||||||
| chr9:136667738 | T | G | 1 | a0001c0007t0001g0048 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-42-503T>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667738 | |||||||
| chr9:136667939 | C | T | 26 | a0001c0001t0001g0064 a0002c0002t0001g0005 a0002c0002t0001g0014 others(23): Show |
47 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.-42-302C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667939 | |||||||
| chr9:136667945 | C | T | 1 | a0001c0003t0003g0146 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-42-296C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667945 | |||||||
| chr9:136667970 | G | A | 3 | a0001c0003t0001g0144 a0001c0003t0001g0145 a0001c0003t0003g0146 |
3 | HG02258.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-42-271G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136667970 | |||||||
| chr9:136668008 | G | A | 2 | a0001c0003t0001g0144 a0001c0003t0001g0145 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-42-233G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136668008 | |||||||
| chr9:136668008 | G | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0090 others(18): Show |
42 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.-42-233G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136668008 | |||||||
| chr9:136668020 | G | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0047 |
3 | HG02451.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-42-221G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136668020 | |||||||
| chr9:136668022 | G | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0047 |
3 | HG02451.hp2 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-42-219G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136668022 | |||||||
| chr9:136668066 | G | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0013g0029 |
4 | HG01106.hp2 HG02055.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42-175G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136668066 | |||||||
| chr9:136668106 | G | A | 4 | a0001c0001t0005g0030 a0001c0003t0001g0144 a0001c0003t0001g0145 others(1): Show |
5 | HG01123.hp2 HG01256.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42-135G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136668106 | |||||||
| chr9:136668186 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-42-55C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 3/10 | chr9 | 136668186 | |||||||
| chr9:136668390 | T | C | 1 | a0002c0002t0006g0086 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.80+28T>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 4/10 | chr9 | 136668390 | |||||||
| chr9:136668529 | T | A | 1 | a0001c0001t0001g0101 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.81-28T>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 4/10 | chr9 | 136668529 | |||||||
| chr9:136668541 | C | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0090 a0001c0001t0001g0091 others(9): Show |
28 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.81-16C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 4/10 | chr9 | 136668541 | |||||||
| chr9:136668692 | C | A | 36 | a0002c0002t0001g0005 a0002c0002t0001g0011 a0002c0002t0001g0014 others(33): Show |
62 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.197+19C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136668692 | |||||||
| chr9:136668811 | T | C | 3 | a0001c0003t0001g0144 a0001c0003t0001g0145 a0001c0003t0003g0146 |
3 | HG02258.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.197+138T>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136668811 | |||||||
| chr9:136668834 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.197+161C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136668834 | |||||||
| chr9:136668922 | TC | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
4 | NA18986.hp1 NA19054.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+253delC | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 136668922 | ||||||
| chr9:136668938 | G | T | 1 | a0001c0007t0001g0048 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.197+265G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136668938 | |||||||
| chr9:136669050 | C | T | 1 | a0001c0007t0001g0048 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.197+377C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669050 | |||||||
| chr9:136669092 | G | T | 1 | a0001c0001t0001g0026 | 3 | HG02683.hp1 HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.197+419G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669092 | |||||||
| chr9:136669232 | TAAG | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0123 |
6 | HG00673.hp1 NA18941.hp2 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-370_198-368del others(3): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr9 | 136669232 | ||||||
| chr9:136669238 | GGGCTCCG others(57): Show |
G | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-367_198-304del others(64): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669238 | |||||||
| chr9:136669268 | C | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0013g0029 |
4 | HG01106.hp2 HG02055.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-338C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669268 | |||||||
| chr9:136669286 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.198-320G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669286 | |||||||
| chr9:136669307 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-299C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669307 | |||||||
| chr9:136669308 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-298C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669308 | |||||||
| chr9:136669309 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-297T>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669309 | |||||||
| chr9:136669315 | C | G | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-291C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669315 | |||||||
| chr9:136669316 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-290C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669316 | |||||||
| chr9:136669317 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-289C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669317 | |||||||
| chr9:136669318 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-288C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669318 | |||||||
| chr9:136669319 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-287C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669319 | |||||||
| chr9:136669320 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-286A>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669320 | |||||||
| chr9:136669323 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-283G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669323 | |||||||
| chr9:136669328 | A | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-278A>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669328 | |||||||
| chr9:136669329 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-277G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669329 | |||||||
| chr9:136669331 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-275C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669331 | |||||||
| chr9:136669335 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-271A>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669335 | |||||||
| chr9:136669338 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-268G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669338 | |||||||
| chr9:136669341 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-265G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669341 | |||||||
| chr9:136669355 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-251G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669355 | |||||||
| chr9:136669356 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-250C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669356 | |||||||
| chr9:136669357 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-249C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669357 | |||||||
| chr9:136669358 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-248T>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669358 | |||||||
| chr9:136669359 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-247G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669359 | |||||||
| chr9:136669360 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-246G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669360 | |||||||
| chr9:136669364 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-242C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669364 | |||||||
| chr9:136669366 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-240G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669366 | |||||||
| chr9:136669367 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-239C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669367 | |||||||
| chr9:136669368 | C | CAGAATGG others(44): Show |
1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-238_198-237ins others(51): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669368 | |||||||
| chr9:136669370 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-236C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669370 | |||||||
| chr9:136669372 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-234G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669372 | |||||||
| chr9:136669374 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-232T>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669374 | |||||||
| chr9:136669375 | C | G | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-231C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669375 | |||||||
| chr9:136669381 | G | A | 3 | a0001c0003t0001g0144 a0001c0003t0001g0145 a0001c0003t0003g0146 |
3 | HG02258.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.198-225G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669381 | |||||||
| chr9:136669384 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-222G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669384 | |||||||
| chr9:136669385 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0006g0020 a0001c0001t0006g0025 |
7 | HG00621.hp2 HG01257.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.198-221T>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669385 | |||||||
| chr9:136669389 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-217G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669389 | |||||||
| chr9:136669391 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-215T>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669391 | |||||||
| chr9:136669392 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-214G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669392 | |||||||
| chr9:136669393 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-213G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669393 | |||||||
| chr9:136669394 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-212G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669394 | |||||||
| chr9:136669397 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.198-209T>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669397 | |||||||
| chr9:136669417 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.198-189C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669417 | |||||||
| chr9:136669481 | T | G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0093 a0001c0001t0001g0104 others(1): Show |
13 | HG00408.hp1 HG02056.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.198-125T>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669481 | |||||||
| chr9:136669490 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.198-116G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669490 | |||||||
| chr9:136669517 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.198-89C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 5/10 | chr9 | 136669517 | |||||||
| chr9:136669781 | G | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0024 others(12): Show |
32 | HG02074.hp1 HG02132.hp1 HG02135.hp2 others(29): Show |
intron_variant | MODIFIER | c.313+60G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 6/10 | chr9 | 136669781 | |||||||
| chr9:136669810 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.313+89C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 6/10 | chr9 | 136669810 | |||||||
| chr9:136670022 | C | G | 31 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0026 others(28): Show |
87 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.409+13C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 7/10 | chr9 | 136670022 | |||||||
| chr9:136670366 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.571+36G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670366 | |||||||
| chr9:136670494 | A | T | 3 | a0001c0001t0001g0020 a0001c0001t0006g0020 a0001c0001t0006g0025 |
7 | HG00621.hp2 HG01257.hp2 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.571+164A>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670494 | |||||||
| chr9:136670499 | G | A | 8 | a0001c0001t0001g0113 a0002c0002t0001g0014 a0002c0002t0001g0036 others(5): Show |
15 | HG00558.hp2 HG00609.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.571+169G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670499 | |||||||
| chr9:136670512 | C | T | 1 | a0001c0001t0001g0040 | 2 | NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.571+182C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670512 | |||||||
| chr9:136670521 | A | C | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.571+191A>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670521 | |||||||
| chr9:136670548 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.571+218C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670548 | |||||||
| chr9:136670592 | G | A | 1 | a0001c0001t0005g0030 | 2 | HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.571+262G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670592 | |||||||
| chr9:136670698 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
309 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.572-252A>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670698 | |||||||
| chr9:136670700 | G | A | 6 | a0001c0001t0001g0010 a0001c0001t0003g0031 a0001c0001t0005g0010 others(3): Show |
10 | HG02055.hp2 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.572-250G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670700 | |||||||
| chr9:136670767 | C | G | 2 | a0001c0001t0010g0066 a0001c0001t0010g0143 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.572-183C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670767 | |||||||
| chr9:136670833 | C | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0029 others(13): Show |
36 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.572-117C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 8/10 | chr9 | 136670833 | |||||||
| chr9:136671027 | TG | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(61): Show |
152 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.636+28delG | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671027 | ||||||
| chr9:136671027 | TGG | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(46): Show |
149 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.636+27_636+28delGG | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671027 | ||||||
| chr9:136671027 | TGGG | T | 34 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0049 others(31): Show |
57 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.636+26_636+28delGG others(1): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671027 | ||||||
| chr9:136671027 | TGGGG | T | 22 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0090 others(19): Show |
46 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.636+25_636+28delGG others(2): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671027 | ||||||
| chr9:136671031 | G | T | 2 | a0002c0002t0001g0035 a0002c0002t0004g0035 |
2 | HG01516.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.636+17G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671031 | |||||||
| chr9:136671035 | G | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0090 others(10): Show |
32 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.636+21G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671035 | |||||||
| chr9:136671036 | G | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(40): Show |
112 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.636+22G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671036 | |||||||
| chr9:136671036 | G | GGGCAGGC others(102): Show |
1 | a0002c0002t0004g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.636+24_636+25insCA others(107): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671036 | ||||||
| chr9:136671040 | G | GGGCAGGC others(240): Show |
1 | a0001c0001t0001g0069 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.636+65_636+311dupG others(246): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671040 | ||||||
| chr9:136671072 | A | T | 1 | a0002c0002t0001g0078 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.636+58A>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671072 | |||||||
| chr9:136671085 | A | AGGGGCAG others(141): Show |
1 | a0001c0001t0005g0030 | 2 | HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.636+92_636+239dupA others(147): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671085 | ||||||
| chr9:136671087 | G | GGGCAGGC others(45): Show |
2 | a0002c0002t0001g0077 a0002c0002t0001g0135 |
2 | HG00558.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.636+92_636+143dupA others(51): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671087 | ||||||
| chr9:136671130 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.636+116C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671130 | |||||||
| chr9:136671139 | A | AGGCAGGC others(41): Show |
3 | a0001c0003t0001g0144 a0001c0003t0001g0145 a0001c0003t0003g0146 |
3 | HG02258.hp2 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.636+207_636+254dup others(48): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671139 | ||||||
| chr9:136671139 | AGGCAGGC others(41): Show |
A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0071 |
3 | HG04228.hp1 NA18974.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.636+207_636+254del others(48): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671139 | ||||||
| chr9:136671152 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.636+138A>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671152 | |||||||
| chr9:136671158 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.636+144G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671158 | |||||||
| chr9:136671174 | T | G | 1 | a0001c0007t0001g0048 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.636+160T>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671174 | |||||||
| chr9:136671180 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.636+166G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671180 | |||||||
| chr9:136671181 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.636+167T>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671181 | |||||||
| chr9:136671231 | G | A | 45 | a0001c0001t0001g0108 a0001c0001t0001g0113 a0001c0001t0004g0107 others(42): Show |
72 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.636+217G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671231 | |||||||
| chr9:136671231 | G | GGGGGGGC others(188): Show |
1 | a0002c0002t0002g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.636+254_636+255ins others(195): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671231 | ||||||
| chr9:136671235 | G | GGGCAGGC others(45): Show |
2 | a0001c0001t0001g0105 a0001c0001t0001g0109 |
2 | NA20752.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.636+255_636+306dup others(52): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671235 | ||||||
| chr9:136671235 | GGGCAGGC others(45): Show |
G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0052 others(2): Show |
11 | HG03017.hp1 NA18747.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.636+255_636+306del others(52): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671235 | ||||||
| chr9:136671240 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0090 others(9): Show |
30 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.636+226G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671240 | |||||||
| chr9:136671269 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
20 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.636+255A>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671269 | |||||||
| chr9:136671281 | G | A | 2 | a0001c0001t0001g0122 a0010c0016t0001g0002 |
2 | NA18954.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.636+267G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671281 | |||||||
| chr9:136671281 | G | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0004c0005t0001g0003 others(1): Show |
4 | HG00544.hp1 HG02080.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.636+267G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671281 | |||||||
| chr9:136671281 | G | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0005g0010 others(1): Show |
4 | HG02055.hp2 HG02572.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.636+267G>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671281 | |||||||
| chr9:136671283 | GGGGA | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0090 a0001c0001t0001g0091 others(2): Show |
20 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.636+272_636+275del others(4): Show |
EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671283 | ||||||
| chr9:136671286 | G | A | 1 | a0001c0015t0014g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.636+272G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671286 | |||||||
| chr9:136671292 | G | A | 1 | a0001c0001t0019g0070 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.636+278G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671292 | |||||||
| chr9:136671326 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
419 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(416): Show |
intron_variant | MODIFIER | c.636+312A>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671326 | |||||||
| chr9:136671479 | C | T | 1 | a0002c0002t0006g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.637-447C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671479 | |||||||
| chr9:136671535 | A | AC | 64 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(61): Show |
103 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.637-385dupC | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 136671535 | ||||||
| chr9:136671568 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0096 others(3): Show |
21 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.637-358C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671568 | |||||||
| chr9:136671619 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.637-307C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671619 | |||||||
| chr9:136671760 | G | C | 1 | a0001c0001t0003g0115 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.637-166G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671760 | |||||||
| chr9:136671799 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.637-127C>G | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671799 | |||||||
| chr9:136671807 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0013g0029 others(1): Show |
4 | HG02572.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-119C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671807 | |||||||
| chr9:136671815 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.637-111G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671815 | |||||||
| chr9:136671836 | G | A | 11 | a0001c0001t0001g0110 a0002c0002t0001g0011 a0002c0002t0001g0035 others(8): Show |
16 | HG00140.hp2 HG00280.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.637-90G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671836 | |||||||
| chr9:136671869 | C | T | 1 | a0002c0002t0003g0080 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.637-57C>T | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 9/10 | chr9 | 136671869 | |||||||
| chr9:136672096 | C | A | 1 | a0002c0002t0002g0072 | 1 | HG01106.hp1 | splice_region_variant&intron_variant | LOW | c.799+8C>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 10/10 | chr9 | 136672096 | |||||||
| chr9:136672221 | G | C | 1 | a0001c0001t0001g0116 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.800-43G>C | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 10/10 | chr9 | 136672221 | |||||||
| chr9:136672247 | G | A | 2 | a0001c0001t0001g0106 a0002c0002t0002g0075 |
2 | HG01192.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.800-17G>A | EGFL7 | ENSG00000172889.16 | transcript | ENST00000308874.12 | protein_coding | 10/10 | chr9 | 136672247 |