Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 392617 |
| ensemblid | ENSG00000225968.8 |
| hgncid | 33154 |
| symbol | ELFN1 |
| name | extracellular leucine rich repeat and fibronectin type III domain containing 1 |
| refseq_nuc | NM_001128636.4 |
| refseq_prot | NP_001122108.1 |
| ensembl_nuc | ENST00000424383.5 |
| ensembl_prot | ENSP00000456548.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 1670277 |
| end | 1747946 |
| strand | + |
| ver | v1.2 |
| region | chr7:1670277-1747946 |
| region5000 | chr7:1665277-1752946 |
| regionname0 | ELFN1_chr7_1670277_1747946 |
| regionname5000 | ELFN1_chr7_1665277_1752946 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 828 | 277 | 79 | 55 | 92 | 13 | 36 | 63 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0002 | 0/0 | 828 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0003 | 0/0 | 828 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGHG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0004 | 0/0 | 828 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0005 | 0/0 | 828 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0006 | 0/0 | 828 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0007 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0008 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0009 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0010 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0011 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0012 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0013 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0014 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| a0015 | 0/0 | 828 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | MAGRG others(823): Show |
chr7 | 1665277 | 1752946 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2484 | 223 | 67 | 49 | 71 | 12 | 23 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0002 | 0/1 | 2484 | 34 | 0 | 4 | 15 | 1 | 13 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0004 | 0/0 | 2484 | 5 | 1 | 0 | 4 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0005 | 0/0 | 2484 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0007 | 0/0 | 2484 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0011 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0014 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0018 | 0/0 | 2484 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0021 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0025 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0026 | 0/0 | 2484 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0001c0027 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0002c0003 | 0/0 | 2484 | 6 | 6 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0002c0024 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0003c0006 | 0/0 | 2484 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0004c0008 | 0/0 | 2484 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0005c0009 | 0/0 | 2484 | 2 | 0 | 0 | 0 | 0 | 2 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0006c0010 | 0/0 | 2484 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0007c0017 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0008c0019 | 0/0 | 2484 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0009c0015 | 0/0 | 2484 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0010c0016 | 0/0 | 2484 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0011c0013 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0012c0022 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0013c0012 | 0/0 | 2484 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0014c0020 | 0/0 | 2484 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 | ||
| a0015c0023 | 0/0 | 2484 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | ATGGC others(2479): Show |
chr7 | 1665277 | 1752946 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3979 | 76 | 18 | 18 | 25 | 6 | 9 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0002 | 1/0 | 3976 | 24 | 1 | 7 | 9 | 2 | 4 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3971): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0003 | 0/0 | 3981 | 7 | 6 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3976): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0004 | 0/0 | 3979 | 7 | 0 | 0 | 7 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0005 | 0/0 | 3982 | 12 | 7 | 1 | 4 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3977): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0006 | 0/0 | 3979 | 8 | 7 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0007 | 0/0 | 3983 | 5 | 0 | 0 | 4 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3978): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0008 | 0/0 | 3984 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3979): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0009 | 0/0 | 3984 | 5 | 1 | 3 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3979): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0011 | 0/0 | 3980 | 5 | 0 | 0 | 4 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3975): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0012 | 0/0 | 3972 | 5 | 1 | 4 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3967): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0013 | 0/0 | 3979 | 5 | 0 | 0 | 5 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0014 | 0/0 | 3976 | 4 | 0 | 3 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3971): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0015 | 0/0 | 3984 | 4 | 0 | 0 | 1 | 0 | 3 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3979): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0016 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3978): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0017 | 0/0 | 3979 | 4 | 0 | 4 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0018 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3970): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0019 | 0/0 | 3985 | 3 | 0 | 1 | 0 | 1 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3980): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0020 | 0/0 | 3981 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3976): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0021 | 0/0 | 3980 | 3 | 0 | 1 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3975): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0022 | 0/0 | 3980 | 3 | 1 | 2 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3975): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0023 | 0/0 | 3976 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3971): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0025 | 0/0 | 3986 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3981): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0026 | 0/0 | 3985 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3980): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0028 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3978): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0029 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3977): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0031 | 0/0 | 3980 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3975): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0033 | 0/0 | 3975 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3970): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0035 | 0/0 | 3979 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0036 | 0/0 | 3976 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3971): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0038 | 0/0 | 3985 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3980): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0039 | 0/0 | 3975 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3970): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0040 | 0/0 | 3987 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3982): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0041 | 0/0 | 3986 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3981): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0042 | 0/0 | 3987 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3982): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0043 | 0/0 | 3985 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3980): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0044 | 0/0 | 3982 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3977): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0047 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3975): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0048 | 0/0 | 3990 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3985): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0049 | 0/0 | 3985 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3980): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0051 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3978): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0052 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3976): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0055 | 0/0 | 3979 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0056 | 0/0 | 3978 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3973): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0059 | 0/0 | 3979 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0060 | 0/0 | 3978 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3973): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0063 | 0/0 | 3979 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0064 | 0/0 | 3983 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3978): Show |
chr7 | 1665277 | 1752946 |
| a0001c0001t0065 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3977): Show |
chr7 | 1665277 | 1752946 |
| a0001c0002t0001 | 0/0 | 3979 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0002t0003 | 0/1 | 3981 | 12 | 0 | 0 | 6 | 1 | 4 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3976): Show |
chr7 | 1665277 | 1752946 |
| a0001c0002t0004 | 0/0 | 3979 | 12 | 0 | 3 | 4 | 0 | 5 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0002t0007 | 0/0 | 3983 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3978): Show |
chr7 | 1665277 | 1752946 |
| a0001c0002t0018 | 0/0 | 3975 | 3 | 0 | 0 | 2 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3970): Show |
chr7 | 1665277 | 1752946 |
| a0001c0002t0027 | 0/0 | 3983 | 2 | 0 | 0 | 1 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3978): Show |
chr7 | 1665277 | 1752946 |
| a0001c0002t0030 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3975): Show |
chr7 | 1665277 | 1752946 |
| a0001c0002t0031 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3975): Show |
chr7 | 1665277 | 1752946 |
| a0001c0002t0053 | 0/0 | 3979 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0004t0034 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3971): Show |
chr7 | 1665277 | 1752946 |
| a0001c0004t0037 | 0/0 | 3978 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3973): Show |
chr7 | 1665277 | 1752946 |
| a0001c0004t0054 | 0/0 | 3980 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3975): Show |
chr7 | 1665277 | 1752946 |
| a0001c0004t0061 | 0/0 | 3977 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3972): Show |
chr7 | 1665277 | 1752946 |
| a0001c0005t0010 | 0/0 | 3983 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3978): Show |
chr7 | 1665277 | 1752946 |
| a0001c0007t0005 | 0/0 | 3982 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3977): Show |
chr7 | 1665277 | 1752946 |
| a0001c0011t0034 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3971): Show |
chr7 | 1665277 | 1752946 |
| a0001c0014t0001 | 0/0 | 3979 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0018t0001 | 0/0 | 3979 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0001c0021t0023 | 0/0 | 3976 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3971): Show |
chr7 | 1665277 | 1752946 |
| a0001c0025t0058 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3971): Show |
chr7 | 1665277 | 1752946 |
| a0001c0026t0057 | 0/0 | 3977 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3972): Show |
chr7 | 1665277 | 1752946 |
| a0001c0027t0062 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3975): Show |
chr7 | 1665277 | 1752946 |
| a0002c0003t0003 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3976): Show |
chr7 | 1665277 | 1752946 |
| a0002c0003t0006 | 0/0 | 3979 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0002c0003t0024 | 0/0 | 3975 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3970): Show |
chr7 | 1665277 | 1752946 |
| a0002c0003t0050 | 0/0 | 3984 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3979): Show |
chr7 | 1665277 | 1752946 |
| a0002c0024t0030 | 0/0 | 3980 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3975): Show |
chr7 | 1665277 | 1752946 |
| a0003c0006t0016 | 0/0 | 3983 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3978): Show |
chr7 | 1665277 | 1752946 |
| a0004c0008t0028 | 0/0 | 3983 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3978): Show |
chr7 | 1665277 | 1752946 |
| a0004c0008t0029 | 0/0 | 3982 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3977): Show |
chr7 | 1665277 | 1752946 |
| a0005c0009t0001 | 0/0 | 3979 | 2 | 0 | 0 | 0 | 0 | 2 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0006c0010t0045 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3976): Show |
chr7 | 1665277 | 1752946 |
| a0006c0010t0046 | 0/0 | 3981 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3976): Show |
chr7 | 1665277 | 1752946 |
| a0007c0017t0001 | 0/0 | 3979 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0008c0019t0001 | 0/0 | 3979 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0009c0015t0032 | 0/0 | 3978 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3973): Show |
chr7 | 1665277 | 1752946 |
| a0010c0016t0001 | 0/0 | 3979 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0011c0013t0020 | 0/0 | 3981 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3976): Show |
chr7 | 1665277 | 1752946 |
| a0012c0022t0001 | 0/0 | 3979 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3974): Show |
chr7 | 1665277 | 1752946 |
| a0013c0012t0032 | 0/0 | 3978 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3973): Show |
chr7 | 1665277 | 1752946 |
| a0014c0020t0002 | 0/0 | 3976 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3971): Show |
chr7 | 1665277 | 1752946 |
| a0015c0023t0003 | 0/0 | 3981 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | AATCC others(3976): Show |
chr7 | 1665277 | 1752946 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0001 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0006g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0006g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0007g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0007g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0007g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0008g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0008g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0009g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0009g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0009g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0011g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0011g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0011g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0011g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0011g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0012g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0012g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0012g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0012g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0012g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0013g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0013g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0013g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0013g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0013g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0014g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0014g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0014g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0014g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0015g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0015g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0015g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0015g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0016g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0017g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0017g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0017g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0017g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0018g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0019g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0019g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0019g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0020g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0020g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0021g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0021g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0021g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0022g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0022g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0022g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0023g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0023g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0025g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0025g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0026g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0026g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0028g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0029g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0031g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0033g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0033g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0035g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0035g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0036g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0036g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0038g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0039g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0040g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0041g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0042g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0043g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0044g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0047g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0048g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0049g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0051g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0052g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0055g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0056g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0059g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0060g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0063g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0064g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0001t0065g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0112 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0007g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0018g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0018g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0018g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0027g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0027g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0030g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0031g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0002t0053g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0004t0034g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0004t0037g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0004t0054g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0004t0061g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0005t0010g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0005t0010g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0005t0010g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0005t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0007t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0007t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0007t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0011t0034g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0014t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0018t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0021t0023g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0025t0058g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0026t0057g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0001c0027t0062g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0002c0003t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0002c0003t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0002c0003t0024g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0002c0003t0024g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0002c0003t0024g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0002c0003t0050g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0002c0024t0030g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0003c0006t0016g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0003c0006t0016g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0003c0006t0016g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0004c0008t0028g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0004c0008t0029g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0005c0009t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0005c0009t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0006c0010t0045g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0006c0010t0046g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0007c0017t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0008c0019t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0009c0015t0032g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0010c0016t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0011c0013t0020g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0012c0022t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0013c0012t0032g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0014c0020t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| a0015c0023t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00280 | hp1 | a0001 | c0001 | t0019 | g0153 | EUR | FIN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | FIN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00408 | hp1 | a0001 | c0001 | t0013 | g0095 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00423 | hp1 | a0001 | c0002 | t0018 | g0040 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00423 | hp2 | a0001 | c0001 | t0013 | g0267 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0164 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0205 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00544 | hp2 | a0007 | c0017 | t0001 | g0216 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00558 | hp1 | a0001 | c0001 | t0023 | g0195 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00558 | hp2 | a0001 | c0001 | t0056 | g0194 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0201 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00639 | hp2 | a0001 | c0001 | t0012 | g0021 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00733 | hp1 | a0001 | c0002 | t0004 | g0256 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00733 | hp2 | a0001 | c0018 | t0001 | g0003 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00735 | hp1 | a0001 | c0001 | t0021 | g0082 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00735 | hp2 | a0001 | c0001 | t0022 | g0252 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00738 | hp1 | a0001 | c0001 | t0014 | g0099 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01070 | hp1 | a0008 | c0019 | t0001 | g0257 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01071 | hp1 | a0001 | c0001 | t0014 | g0075 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01074 | hp1 | a0001 | c0001 | t0014 | g0180 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01074 | hp2 | a0001 | c0001 | t0022 | g0076 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01099 | hp1 | a0001 | c0001 | t0017 | g0084 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01099 | hp2 | a0001 | c0001 | t0019 | g0123 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01106 | hp2 | a0001 | c0002 | t0004 | g0063 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01167 | hp1 | a0001 | c0001 | t0012 | g0211 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01167 | hp2 | a0001 | c0001 | t0012 | g0183 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01168 | hp1 | a0001 | c0001 | t0009 | g0052 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01169 | hp1 | a0001 | c0001 | t0012 | g0210 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0051 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01175 | hp1 | a0001 | c0001 | t0009 | g0120 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01175 | hp2 | a0001 | c0002 | t0004 | g0152 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01243 | hp1 | a0001 | c0001 | t0005 | g0155 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01243 | hp2 | a0001 | c0001 | t0048 | g0125 | AMR | PUR | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01255 | hp1 | a0001 | c0001 | t0064 | g0014 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01358 | hp2 | a0001 | c0001 | t0017 | g0196 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01433 | hp1 | a0001 | c0001 | t0017 | g0103 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01433 | hp2 | a0001 | c0001 | t0059 | g0085 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01496 | hp1 | a0009 | c0015 | t0032 | g0190 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01515 | hp1 | a0001 | c0001 | t0014 | g0078 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0111 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0171 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01517 | hp1 | a0001 | c0001 | t0039 | g0172 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | IBS | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01884 | hp1 | a0001 | c0001 | t0022 | g0261 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01884 | hp2 | a0001 | c0011 | t0034 | g0015 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0122 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01891 | hp2 | a0001 | c0001 | t0028 | g0081 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01975 | hp2 | a0001 | c0002 | t0007 | g0058 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01993 | hp1 | a0010 | c0016 | t0001 | g0277 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01993 | hp2 | a0001 | c0001 | t0017 | g0101 | AMR | PEL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0285 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02071 | hp1 | a0001 | c0014 | t0001 | g0008 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02074 | hp1 | a0001 | c0001 | t0015 | g0162 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02074 | hp2 | a0001 | c0002 | t0018 | g0228 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02083 | hp1 | a0001 | c0001 | t0021 | g0259 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0224 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02145 | hp1 | a0002 | c0003 | t0024 | g0182 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0148 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | CDX | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | CDX | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CDX | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | CDX | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02257 | hp1 | a0002 | c0003 | t0006 | g0013 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02258 | hp1 | a0001 | c0001 | t0065 | g0286 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02258 | hp2 | a0001 | c0001 | t0020 | g0017 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02280 | hp1 | a0001 | c0027 | t0062 | g0199 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02280 | hp2 | a0001 | c0001 | t0055 | g0288 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02451 | hp1 | a0001 | c0001 | t0020 | g0133 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02572 | hp2 | a0011 | c0013 | t0020 | g0093 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02602 | hp2 | a0001 | c0002 | t0004 | g0260 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02615 | hp1 | a0001 | c0001 | t0018 | g0138 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0029 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02622 | hp1 | a0001 | c0001 | t0025 | g0054 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02622 | hp2 | a0001 | c0001 | t0026 | g0136 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02630 | hp1 | a0001 | c0001 | t0051 | g0019 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02630 | hp2 | a0001 | c0005 | t0010 | g0004 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0018 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02647 | hp2 | a0003 | c0006 | t0016 | g0181 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02698 | hp1 | a0001 | c0002 | t0018 | g0041 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02698 | hp2 | a0001 | c0002 | t0004 | g0050 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02723 | hp1 | a0001 | c0004 | t0034 | g0127 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02723 | hp2 | a0001 | c0001 | t0029 | g0031 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02735 | hp1 | a0001 | c0001 | t0040 | g0048 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0270 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0242 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0149 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0119 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02818 | hp2 | a0001 | c0001 | t0025 | g0012 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02886 | hp1 | a0001 | c0005 | t0010 | g0004 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02896 | hp1 | a0001 | c0001 | t0035 | g0055 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02976 | hp1 | a0004 | c0008 | t0029 | g0283 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02976 | hp2 | a0001 | c0001 | t0038 | g0287 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0192 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03098 | hp2 | a0001 | c0005 | t0010 | g0144 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03139 | hp2 | a0003 | c0006 | t0016 | g0200 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03195 | hp1 | a0001 | c0007 | t0005 | g0130 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0132 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03209 | hp2 | a0012 | c0022 | t0001 | g0033 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03225 | hp1 | a0001 | c0001 | t0049 | g0025 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03225 | hp2 | a0001 | c0005 | t0010 | g0147 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0137 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0124 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03486 | hp2 | a0002 | c0003 | t0003 | g0022 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03491 | hp1 | a0001 | c0002 | t0003 | g0243 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03491 | hp2 | a0001 | c0001 | t0019 | g0064 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03516 | hp2 | a0002 | c0003 | t0024 | g0145 | AFR | ESN | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03540 | hp1 | a0001 | c0001 | t0026 | g0020 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03540 | hp2 | a0001 | c0005 | t0010 | g0142 | AFR | GWD | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03579 | hp1 | a0001 | c0001 | t0052 | g0034 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03579 | hp2 | a0013 | c0012 | t0032 | g0158 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03669 | hp1 | a0001 | c0001 | t0015 | g0169 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03704 | hp1 | a0001 | c0001 | t0011 | g0104 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03704 | hp2 | a0001 | c0002 | t0003 | g0105 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03710 | hp1 | a0005 | c0009 | t0001 | g0110 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03710 | hp2 | a0001 | c0001 | t0015 | g0264 | SAS | PJL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0265 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03927 | hp1 | a0001 | c0002 | t0027 | g0057 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03942 | hp1 | a0001 | c0002 | t0004 | g0280 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03942 | hp2 | a0001 | c0002 | t0003 | g0188 | SAS | BEB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG04115 | hp1 | a0001 | c0001 | t0042 | g0165 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0266 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG04199 | hp2 | a0001 | c0002 | t0053 | g0118 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG04204 | hp1 | a0005 | c0009 | t0001 | g0249 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG04204 | hp2 | a0001 | c0001 | t0031 | g0102 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG04228 | hp1 | a0001 | c0001 | t0041 | g0170 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18522 | hp2 | a0002 | c0024 | t0030 | g0028 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18612 | hp1 | a0001 | c0001 | t0011 | g0240 | EAS | CHB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | CHB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0282 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18941 | hp1 | a0001 | c0001 | t0013 | g0091 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18943 | hp1 | a0001 | c0001 | t0033 | g0247 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18943 | hp2 | a0001 | c0004 | t0037 | g0009 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0167 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18944 | hp2 | a0001 | c0004 | t0037 | g0009 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18945 | hp2 | a0014 | c0020 | t0002 | g0062 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0237 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18948 | hp1 | a0001 | c0001 | t0044 | g0217 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18948 | hp2 | a0001 | c0001 | t0011 | g0086 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18953 | hp2 | a0001 | c0021 | t0023 | g0193 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18959 | hp1 | a0001 | c0004 | t0061 | g0269 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18963 | hp1 | a0001 | c0001 | t0011 | g0212 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0166 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18964 | hp1 | a0001 | c0001 | t0011 | g0106 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18964 | hp2 | a0001 | c0002 | t0030 | g0007 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18977 | hp1 | a0001 | c0001 | t0021 | g0268 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18977 | hp2 | a0001 | c0002 | t0003 | g0220 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18980 | hp1 | a0001 | c0002 | t0004 | g0248 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18980 | hp2 | a0001 | c0001 | t0023 | g0227 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18983 | hp1 | a0001 | c0002 | t0004 | g0096 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0250 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19000 | hp2 | a0001 | c0002 | t0004 | g0235 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19003 | hp1 | a0006 | c0010 | t0045 | g0150 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19003 | hp2 | a0001 | c0001 | t0060 | g0245 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19004 | hp2 | a0001 | c0002 | t0027 | g0189 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0218 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19009 | hp2 | a0001 | c0001 | t0043 | g0163 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19030 | hp1 | a0002 | c0003 | t0024 | g0045 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19030 | hp2 | a0001 | c0007 | t0005 | g0128 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19043 | hp1 | a0001 | c0025 | t0058 | g0046 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0038 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19055 | hp1 | a0001 | c0004 | t0054 | g0168 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19055 | hp2 | a0001 | c0001 | t0033 | g0276 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0007 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19060 | hp2 | a0006 | c0010 | t0046 | g0151 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19065 | hp1 | a0001 | c0001 | t0013 | g0198 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19065 | hp2 | a0001 | c0001 | t0013 | g0230 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19066 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19074 | hp2 | a0001 | c0002 | t0031 | g0236 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0214 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19082 | hp2 | a0001 | c0001 | t0036 | g0273 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19089 | hp2 | a0001 | c0001 | t0036 | g0139 | EAS | JPT | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0039 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0161 | AFR | YRI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA20129 | hp2 | a0002 | c0003 | t0050 | g0178 | AFR | ASW | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA20752 | hp1 | a0001 | c0001 | t0009 | g0121 | EUR | TSI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA20805 | hp2 | a0015 | c0023 | t0003 | g0131 | EUR | TSI | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA20905 | hp1 | a0001 | c0001 | t0015 | g0175 | SAS | GIH | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA20905 | hp2 | a0001 | c0002 | t0004 | g0049 | SAS | GIH | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01123 | hp1 | a0001 | c0026 | t0057 | g0186 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02109 | hp2 | a0001 | c0007 | t0005 | g0184 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0129 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0291 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0056 | AFR | ACB | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03471 | hp1 | a0003 | c0006 | t0016 | g0141 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG03471 | hp2 | a0004 | c0008 | t0028 | g0284 | AFR | MSL | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG06807 | hp1 | a0001 | c0001 | t0063 | g0072 | AFR | USA | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | USA | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA20300 | hp1 | a0001 | c0001 | t0047 | g0059 | AFR | USA | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | USA | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| NA21309 | hp2 | a0001 | c0001 | t0035 | g0281 | AFR | LWK | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0003 | g0112 | REF | REF | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | ELFN1_chr7_1665277_1752946 | ELFN1 | chr7 | 1665277 | 1752946 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:1744607 | G | A | 1 | a0003 | 3 | HG02647.hp2 HG03139.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.11G>A | p.Arg4His | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 637/3976 | 11/2487 | 4/828 | chr7 | 1744607 | |||
| chr7:1744885 | G | A | 1 | a0004 | 2 | HG02976.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.289G>A | p.Gly97Ser | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 915/3976 | 289/2487 | 97/828 | chr7 | 1744885 | |||
| chr7:1745543 | G | A | 1 | a0013 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.947G>A | p.Arg316His | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1573/3976 | 947/2487 | 316/828 | chr7 | 1745543 | |||
| chr7:1745902 | G | A | 1 | a0011 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1306G>A | p.Val436Ile | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1932/3976 | 1306/2487 | 436/828 | chr7 | 1745902 | |||
| chr7:1746026 | C | T | 1 | a0015 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1430C>T | p.Ala477Val | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2056/3976 | 1430/2487 | 477/828 | chr7 | 1746026 | |||
| chr7:1746484 | G | A | 3 | a0002 a0009 a0013 |
9 | HG01496.hp1 HG02145.hp1 HG02257.hp1 others(6): Show |
missense_variant | MODERATE | c.1888G>A | p.Val630Met | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2514/3976 | 1888/2487 | 630/828 | chr7 | 1746484 | |||
| chr7:1746494 | C | G | 1 | a0012 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.1898C>G | p.Ala633Gly | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2524/3976 | 1898/2487 | 633/828 | chr7 | 1746494 | |||
| chr7:1746554 | G | C | 1 | a0010 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.1958G>C | p.Arg653Pro | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2584/3976 | 1958/2487 | 653/828 | chr7 | 1746554 | |||
| chr7:1746623 | C | T | 1 | a0009 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.2027C>T | p.Ala676Val | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2653/3976 | 2027/2487 | 676/828 | chr7 | 1746623 | |||
| chr7:1746661 | G | A | 1 | a0005 | 2 | HG03710.hp1 HG04204.hp1 |
missense_variant | MODERATE | c.2065G>A | p.Val689Met | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2691/3976 | 2065/2487 | 689/828 | chr7 | 1746661 | |||
| chr7:1746773 | C | T | 1 | a0014 | 1 | NA18945.hp2 | missense_variant | MODERATE | c.2177C>T | p.Pro726Leu | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2803/3976 | 2177/2487 | 726/828 | chr7 | 1746773 | |||
| chr7:1746895 | G | A | 1 | a0007 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.2299G>A | p.Glu767Lys | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2925/3976 | 2299/2487 | 767/828 | chr7 | 1746895 | |||
| chr7:1746952 | C | T | 1 | a0008 | 1 | HG01070.hp1 | missense_variant | MODERATE | c.2356C>T | p.Arg786Trp | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2982/3976 | 2356/2487 | 786/828 | chr7 | 1746952 | |||
| chr7:1746968 | A | T | 1 | a0006 | 2 | NA19003.hp1 NA19060.hp2 |
missense_variant | MODERATE | c.2372A>T | p.Glu791Val | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2998/3976 | 2372/2487 | 791/828 | chr7 | 1746968 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:1744656 | C | T | 1 | a0001c0027 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.60C>T | p.His20His | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 686/3976 | 60/2487 | 20/828 | chr7 | 1744656 | |||
| chr7:1744911 | G | A | 2 | a0001c0004 a0001c0011 |
6 | HG01884.hp2 HG02723.hp1 NA18943.hp2 others(3): Show |
synonymous_variant | LOW | c.315G>A | p.Ser105Ser | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 941/3976 | 315/2487 | 105/828 | chr7 | 1744911 | |||
| chr7:1745280 | C | G | 1 | a0001c0026 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.684C>G | p.Gly228Gly | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1310/3976 | 684/2487 | 228/828 | chr7 | 1745280 | |||
| chr7:1745355 | C | T | 1 | a0001c0025 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.759C>T | p.Asp253Asp | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1385/3976 | 759/2487 | 253/828 | chr7 | 1745355 | |||
| chr7:1745361 | C | T | 1 | a0001c0011 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.765C>T | p.Tyr255Tyr | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1391/3976 | 765/2487 | 255/828 | chr7 | 1745361 | |||
| chr7:1745592 | C | T | 1 | a0002c0024 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.996C>T | p.Thr332Thr | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1622/3976 | 996/2487 | 332/828 | chr7 | 1745592 | |||
| chr7:1745832 | C | T | 1 | a0001c0027 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1236C>T | p.Pro412Pro | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 1862/3976 | 1236/2487 | 412/828 | chr7 | 1745832 | |||
| chr7:1746066 | C | A | 1 | a0001c0014 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1470C>A | p.Gly490Gly | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2096/3976 | 1470/2487 | 490/828 | chr7 | 1746066 | |||
| chr7:1746102 | G | A | 3 | a0001c0002 a0001c0026 a0015c0023 |
35 | HG00423.hp1 HG00733.hp1 HG01106.hp2 others(32): Show |
synonymous_variant | LOW | c.1506G>A | p.Ala502Ala | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2132/3976 | 1506/2487 | 502/828 | chr7 | 1746102 | |||
| chr7:1746537 | C | T | 1 | a0001c0007 | 3 | HG02109.hp2 HG03195.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.1941C>T | p.Arg647Arg | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2567/3976 | 1941/2487 | 647/828 | chr7 | 1746537 | |||
| chr7:1746558 | C | T | 1 | a0001c0021 | 1 | NA18953.hp2 | synonymous_variant | LOW | c.1962C>T | p.Ala654Ala | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 2588/3976 | 1962/2487 | 654/828 | chr7 | 1746558 | |||
| chr7:1746987 | C | T | 1 | a0001c0018 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.2391C>T | p.Gly797Gly | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 3017/3976 | 2391/2487 | 797/828 | chr7 | 1746987 | |||
| chr7:1747065 | G | A | 1 | a0001c0005 | 5 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.2469G>A | p.Ser823Ser | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 3095/3976 | 2469/2487 | 823/828 | chr7 | 1747065 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:1688063 | G | A | 1 | a0001c0001t0038 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-543G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/4 | 56534 | chr7 | 1688063 | ||||||
| chr7:1688110 | C | T | 1 | a0001c0001t0065 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-496C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/4 | 56487 | chr7 | 1688110 | ||||||
| chr7:1688121 | C | T | 1 | a0001c0001t0064 | 1 | HG01255.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-485C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/4 | chr7 | 1688121 | |||||||
| chr7:1709095 | A | G | 1 | a0001c0001t0063 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-451A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/4 | 35502 | chr7 | 1709095 | ||||||
| chr7:1709106 | C | T | 1 | a0001c0027t0062 | 1 | HG02280.hp1 | 5_prime_UTR_variant | MODIFIER | c.-440C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/4 | 35491 | chr7 | 1709106 | ||||||
| chr7:1744490 | C | A | 2 | a0001c0001t0014 a0001c0001t0039 |
5 | HG00738.hp1 HG01071.hp1 HG01074.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-107C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 107 | chr7 | 1744490 | ||||||
| chr7:1744518 | C | T | 2 | a0001c0004t0037 a0001c0004t0061 |
3 | NA18943.hp2 NA18944.hp2 NA18959.hp1 |
5_prime_UTR_variant | MODIFIER | c.-79C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 79 | chr7 | 1744518 | ||||||
| chr7:1747132 | C | T | 1 | a0001c0001t0036 | 2 | NA19082.hp2 NA19089.hp2 |
3_prime_UTR_variant | MODIFIER | c.*49C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 49 | chr7 | 1747132 | ||||||
| chr7:1747182 | T | C | 13 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0016 others(10): Show |
24 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*99T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 99 | chr7 | 1747182 | ||||||
| chr7:1747208 | C | T | 1 | a0002c0003t0024 | 3 | HG02145.hp1 HG03516.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*125C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 125 | chr7 | 1747208 | ||||||
| chr7:1747209 | G | A | 11 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0017 others(8): Show |
23 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*126G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 126 | chr7 | 1747209 | ||||||
| chr7:1747249 | C | T | 1 | a0001c0001t0035 | 2 | HG02896.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*166C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 166 | chr7 | 1747249 | ||||||
| chr7:1747283 | C | T | 2 | a0001c0001t0023 a0001c0021t0023 |
3 | HG00558.hp1 NA18953.hp2 NA18980.hp2 |
3_prime_UTR_variant | MODIFIER | c.*200C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 200 | chr7 | 1747283 | ||||||
| chr7:1747289 | G | A | 1 | a0001c0001t0047 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*206G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 206 | chr7 | 1747289 | ||||||
| chr7:1747302 | C | CCA | 4 | a0001c0001t0056 a0001c0004t0037 a0001c0004t0061 others(1): Show |
5 | HG00558.hp2 HG01123.hp1 NA18943.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*251_*252dupAC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | |||||
| chr7:1747302 | C | CCACA | 15 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0031 others(12): Show |
37 | HG00408.hp2 HG00544.hp1 HG00733.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*249_*252dupACAC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | |||||
| chr7:1747302 | C | CCACACA | 18 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(15): Show |
55 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*247_*252dupACACAC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | |||||
| chr7:1747302 | C | CCACACAC others(1): Show |
10 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0015 others(7): Show |
26 | HG00280.hp1 HG01099.hp2 HG01168.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*245_*252dupACACAC others(2): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | |||||
| chr7:1747302 | C | CCACACAC others(3): Show |
8 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0038 others(5): Show |
10 | HG02622.hp1 HG02622.hp2 HG02735.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*243_*252dupACACAC others(4): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | |||||
| chr7:1747302 | C | CCACACAC others(7): Show |
1 | a0001c0001t0048 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*239_*252dupACACAC others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 253 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | |||||
| chr7:1747302 | CCACA | C | 1 | a0001c0001t0012 | 5 | HG00639.hp2 HG01167.hp1 HG01167.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*249_*252delACAC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 249 | INFO_REALIGN_3_PRIME | chr7 | 1747302 | |||||
| chr7:1747313 | C | CACAG | 20 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0013 others(17): Show |
115 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*233_*234insGACA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 234 | INFO_REALIGN_3_PRIME | chr7 | 1747313 | |||||
| chr7:1747361 | A | C | 1 | a0001c0001t0035 | 2 | HG02896.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*278A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 278 | chr7 | 1747361 | ||||||
| chr7:1747367 | G | C | 20 | a0001c0001t0001 a0001c0001t0013 a0001c0001t0017 others(17): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*284G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 284 | chr7 | 1747367 | ||||||
| chr7:1747465 | T | A | 1 | a0001c0025t0058 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*382T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 382 | chr7 | 1747465 | ||||||
| chr7:1747570 | G | A | 1 | a0001c0001t0013 | 5 | HG00408.hp1 HG00423.hp2 NA18941.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*487G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 487 | chr7 | 1747570 | ||||||
| chr7:1747600 | A | G | 29 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0013 others(26): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*517A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 517 | chr7 | 1747600 | ||||||
| chr7:1747765 | G | A | 1 | a0001c0001t0059 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*682G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 682 | chr7 | 1747765 | ||||||
| chr7:1747790 | T | C | 6 | a0001c0001t0031 a0001c0001t0040 a0001c0001t0041 others(3): Show |
7 | HG02735.hp1 HG04204.hp2 HG04228.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*707T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 707 | chr7 | 1747790 | ||||||
| chr7:1747823 | A | G | 1 | a0001c0005t0010 | 5 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*740A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 740 | chr7 | 1747823 | ||||||
| chr7:1747883 | T | TA | 13 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0020 others(10): Show |
24 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*817dupA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 818 | INFO_REALIGN_3_PRIME | chr7 | 1747883 | |||||
| chr7:1747883 | TA | T | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(37): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*817delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 817 | INFO_REALIGN_3_PRIME | chr7 | 1747883 | |||||
| chr7:1747883 | TAA | T | 6 | a0001c0001t0060 a0001c0002t0030 a0002c0003t0050 others(3): Show |
6 | HG01496.hp1 HG03579.hp2 NA18522.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*816_*817delAA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 816 | INFO_REALIGN_3_PRIME | chr7 | 1747883 | |||||
| chr7:1747938 | C | A | 71 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(68): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*855C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 4/4 | 855 | chr7 | 1747938 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:1670395 | T | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | HG01361.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-549+41T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670395 | |||||||
| chr7:1670531 | G | A | 2 | a0001c0001t0025g0012 a0002c0003t0006g0013 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-549+177G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670531 | |||||||
| chr7:1670595 | G | T | 1 | a0001c0001t0004g0292 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-549+241G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670595 | |||||||
| chr7:1670630 | GC | G | 5 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0003g0291 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-549+280delC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1670630 | ||||||
| chr7:1670831 | C | G | 2 | a0001c0001t0005g0285 a0001c0001t0065g0286 |
2 | HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-549+477C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670831 | |||||||
| chr7:1670880 | C | T | 2 | a0004c0008t0028g0284 a0004c0008t0029g0283 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-549+526C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670880 | |||||||
| chr7:1670922 | C | T | 2 | a0001c0001t0006g0282 a0001c0001t0035g0281 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-549+568C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670922 | |||||||
| chr7:1670929 | C | G | 1 | a0001c0002t0004g0280 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-549+575C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1670929 | |||||||
| chr7:1670983 | AC | A | 49 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0238 others(46): Show |
52 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.-549+633delC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1670983 | ||||||
| chr7:1671170 | G | GC | 49 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0001t0001g0154 others(46): Show |
50 | HG00280.hp1 HG00438.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.-549+827dupC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671170 | ||||||
| chr7:1671170 | G | GCC | 14 | a0001c0001t0001g0187 a0001c0001t0001g0191 a0001c0001t0002g0197 others(11): Show |
14 | HG00558.hp1 HG00558.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.-549+826_-549+827d others(4): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671170 | ||||||
| chr7:1671170 | G | GCCC | 23 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0209 others(20): Show |
23 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.-549+825_-549+827d others(5): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671170 | ||||||
| chr7:1671170 | G | GCCCC | 15 | a0001c0001t0001g0229 a0001c0001t0001g0233 a0001c0001t0001g0234 others(12): Show |
15 | HG00438.hp2 HG02074.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.-549+824_-549+827d others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671170 | ||||||
| chr7:1671170 | GC | G | 67 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(64): Show |
70 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-549+827delC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671170 | ||||||
| chr7:1671362 | G | C | 2 | a0001c0001t0025g0012 a0002c0003t0006g0013 |
2 | HG02257.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-549+1008G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671362 | |||||||
| chr7:1671403 | T | G | 75 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(72): Show |
79 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-549+1049T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671403 | |||||||
| chr7:1671406 | A | G | 1 | a0001c0026t0057g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-549+1052A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671406 | |||||||
| chr7:1671426 | T | G | 77 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(74): Show |
81 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.-549+1072T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671426 | |||||||
| chr7:1671637 | GA | G | 9 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0003g0032 others(6): Show |
9 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-549+1286delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1671637 | ||||||
| chr7:1671958 | T | G | 38 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0154 others(35): Show |
38 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.-549+1604T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671958 | |||||||
| chr7:1671990 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.-549+1636T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671990 | |||||||
| chr7:1671992 | T | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.-549+1638T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671992 | |||||||
| chr7:1671993 | C | A | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.-549+1639C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671993 | |||||||
| chr7:1671995 | A | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.-549+1641A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1671995 | |||||||
| chr7:1672061 | C | G | 1 | a0001c0001t0002g0222 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-549+1707C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672061 | |||||||
| chr7:1672066 | G | A | 2 | a0001c0001t0006g0039 a0001c0025t0058g0046 |
2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-549+1712G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672066 | |||||||
| chr7:1672072 | G | C | 3 | a0001c0001t0001g0187 a0001c0001t0003g0047 a0001c0001t0005g0149 |
3 | HG01109.hp2 HG02809.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-549+1718G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672072 | |||||||
| chr7:1672077 | G | A | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-549+1723G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672077 | |||||||
| chr7:1672145 | G | C | 1 | a0009c0015t0032g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-549+1791G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672145 | |||||||
| chr7:1672418 | C | T | 3 | a0001c0001t0003g0185 a0001c0005t0010g0142 a0003c0006t0016g0141 |
3 | HG03471.hp1 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-549+2064C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672418 | |||||||
| chr7:1672460 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0003g0047 |
2 | HG01109.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-549+2106C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672460 | |||||||
| chr7:1672494 | T | C | 6 | a0001c0001t0001g0143 a0001c0001t0001g0146 a0001c0005t0010g0004 others(3): Show |
7 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-549+2140T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672494 | |||||||
| chr7:1672699 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0036g0139 a0001c0001t0036g0273 |
3 | NA18970.hp1 NA19082.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.-549+2345C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672699 | |||||||
| chr7:1672735 | C | A | 2 | a0001c0002t0018g0040 a0001c0002t0018g0041 |
2 | HG00423.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-549+2381C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672735 | |||||||
| chr7:1672737 | C | T | 1 | a0001c0001t0003g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-549+2383C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672737 | |||||||
| chr7:1672850 | A | G | 41 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0126 others(38): Show |
41 | HG01099.hp2 HG01167.hp2 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.-549+2496A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672850 | |||||||
| chr7:1672923 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-549+2569C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672923 | |||||||
| chr7:1672934 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-549+2580C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672934 | |||||||
| chr7:1672997 | G | A | 1 | a0001c0001t0040g0048 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-549+2643G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1672997 | |||||||
| chr7:1673054 | G | A | 1 | a0001c0001t0003g0185 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-549+2700G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673054 | |||||||
| chr7:1673093 | C | CCT | 123 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(120): Show |
127 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-549+2740_-549+274 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1673093 | ||||||
| chr7:1673093 | C | CT | 83 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(80): Show |
83 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-549+2739_-549+274 others(5): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673093 | |||||||
| chr7:1673093 | C | T | 4 | a0001c0001t0013g0198 a0001c0002t0004g0235 a0001c0002t0004g0237 others(1): Show |
4 | NA18947.hp2 NA19000.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-549+2739C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673093 | |||||||
| chr7:1673184 | G | T | 168 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(165): Show |
172 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-549+2830G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673184 | |||||||
| chr7:1673234 | C | G | 1 | a0001c0001t0003g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-549+2880C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673234 | |||||||
| chr7:1673250 | G | A | 1 | a0001c0001t0006g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-549+2896G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673250 | |||||||
| chr7:1673303 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0143 a0001c0001t0003g0047 others(2): Show |
5 | HG01109.hp2 HG02055.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.-549+2949A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673303 | |||||||
| chr7:1673373 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-549+3019G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673373 | |||||||
| chr7:1673519 | C | A | 1 | a0001c0001t0019g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-549+3165C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673519 | |||||||
| chr7:1673584 | G | A | 19 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0154 others(16): Show |
19 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-549+3230G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673584 | |||||||
| chr7:1673639 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 |
3 | HG00140.hp2 HG03831.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-549+3285C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673639 | |||||||
| chr7:1673804 | T | C | 1 | a0002c0003t0024g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-549+3450T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673804 | |||||||
| chr7:1673813 | G | A | 1 | a0005c0009t0001g0110 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-549+3459G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673813 | |||||||
| chr7:1673996 | G | A | 3 | a0001c0001t0005g0285 a0001c0001t0048g0125 a0001c0001t0055g0288 |
3 | HG01243.hp2 HG02055.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-549+3642G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1673996 | |||||||
| chr7:1674053 | G | A | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-549+3699G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674053 | |||||||
| chr7:1674082 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0143 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-549+3728C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674082 | |||||||
| chr7:1674250 | G | A | 1 | a0001c0002t0003g0111 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-549+3896G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674250 | |||||||
| chr7:1674401 | G | A | 3 | a0001c0001t0001g0191 a0001c0001t0008g0192 a0009c0015t0032g0190 |
3 | HG01496.hp1 HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-549+4047G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674401 | |||||||
| chr7:1674439 | G | C | 167 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(164): Show |
170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.-549+4085G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674439 | |||||||
| chr7:1674500 | A | G | 1 | a0001c0027t0062g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-549+4146A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674500 | |||||||
| chr7:1674629 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0047g0059 |
2 | HG01109.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-549+4275G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674629 | |||||||
| chr7:1674636 | C | G | 1 | a0001c0001t0012g0183 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-549+4282C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674636 | |||||||
| chr7:1674641 | G | A | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-549+4287G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674641 | |||||||
| chr7:1674812 | G | C | 137 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(134): Show |
140 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-549+4458G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674812 | |||||||
| chr7:1674844 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0061 others(2): Show |
5 | HG00741.hp2 HG01361.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-549+4490G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674844 | |||||||
| chr7:1674878 | T | C | 6 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0005g0161 others(3): Show |
6 | HG01081.hp1 HG02922.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-549+4524T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674878 | |||||||
| chr7:1674911 | A | G | 1 | a0001c0001t0011g0106 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-549+4557A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674911 | |||||||
| chr7:1674949 | G | A | 1 | a0001c0027t0062g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-549+4595G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1674949 | |||||||
| chr7:1675023 | G | A | 1 | a0001c0021t0023g0193 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-549+4669G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675023 | |||||||
| chr7:1675027 | T | TCCCCACA others(24): Show |
165 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(162): Show |
168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.-549+4674_-549+470 others(35): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1675027 | ||||||
| chr7:1675043 | C | CCGGGCTC others(24): Show |
1 | a0001c0001t0013g0230 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-549+4704_-549+470 others(35): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1675043 | ||||||
| chr7:1675067 | T | C | 169 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(166): Show |
172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.-549+4713T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675067 | |||||||
| chr7:1675094 | C | G | 168 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0016 others(165): Show |
171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-549+4740C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675094 | |||||||
| chr7:1675208 | T | A | 46 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0238 others(43): Show |
48 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.-549+4854T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675208 | |||||||
| chr7:1675272 | G | A | 4 | a0001c0001t0008g0124 a0001c0001t0008g0132 a0001c0001t0020g0133 others(1): Show |
4 | HG02451.hp1 HG03195.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-549+4918G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675272 | |||||||
| chr7:1675326 | T | C | 19 | a0001c0001t0001g0126 a0001c0001t0001g0146 a0001c0001t0001g0289 others(16): Show |
20 | HG01168.hp1 HG01169.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.-549+4972T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675326 | |||||||
| chr7:1675332 | G | A | 3 | a0001c0001t0006g0119 a0001c0001t0016g0038 a0002c0003t0024g0045 |
3 | HG02818.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-549+4978G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675332 | |||||||
| chr7:1675360 | C | T | 2 | a0001c0001t0012g0183 a0002c0003t0024g0182 |
2 | HG01167.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-549+5006C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675360 | |||||||
| chr7:1675406 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-549+5052C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675406 | |||||||
| chr7:1675477 | C | T | 1 | a0001c0011t0034g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-549+5123C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675477 | |||||||
| chr7:1675556 | C | T | 1 | a0001c0002t0004g0237 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-549+5202C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675556 | |||||||
| chr7:1675708 | G | A | 3 | a0001c0001t0001g0191 a0001c0001t0008g0192 a0009c0015t0032g0190 |
3 | HG01496.hp1 HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-549+5354G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675708 | |||||||
| chr7:1675735 | C | T | 1 | a0003c0006t0016g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-549+5381C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675735 | |||||||
| chr7:1675738 | T | C | 1 | a0002c0003t0050g0178 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-549+5384T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675738 | |||||||
| chr7:1675841 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-549+5487C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675841 | |||||||
| chr7:1675855 | C | T | 11 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0185 others(8): Show |
11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-549+5501C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675855 | |||||||
| chr7:1675883 | C | T | 1 | a0001c0002t0003g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-549+5529C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1675883 | |||||||
| chr7:1676011 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-549+5657A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676011 | |||||||
| chr7:1676029 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0003g0291 a0001c0001t0038g0287 |
3 | HG02559.hp1 HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-549+5675C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676029 | |||||||
| chr7:1676156 | G | C | 1 | a0014c0020t0002g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-549+5802G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676156 | |||||||
| chr7:1676263 | C | T | 1 | a0001c0001t0011g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-549+5909C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676263 | |||||||
| chr7:1676435 | C | T | 3 | a0001c0001t0006g0119 a0001c0001t0016g0038 a0002c0003t0050g0178 |
3 | HG02818.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-549+6081C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676435 | |||||||
| chr7:1676448 | G | A | 1 | a0001c0001t0016g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-549+6094G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676448 | |||||||
| chr7:1676580 | G | T | 1 | a0001c0011t0034g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-549+6226G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676580 | |||||||
| chr7:1676642 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-549+6288C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676642 | |||||||
| chr7:1676718 | G | A | 3 | a0001c0001t0005g0149 a0001c0001t0019g0123 a0001c0001t0020g0017 |
3 | HG01099.hp2 HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-549+6364G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676718 | |||||||
| chr7:1676854 | C | T | 1 | a0002c0003t0003g0022 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-549+6500C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676854 | |||||||
| chr7:1676934 | C | T | 1 | a0001c0001t0005g0219 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-549+6580C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1676934 | |||||||
| chr7:1677025 | C | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0157 a0001c0001t0001g0159 others(47): Show |
51 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-549+6671C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677025 | |||||||
| chr7:1677037 | G | A | 1 | a0001c0001t0006g0119 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-549+6683G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677037 | |||||||
| chr7:1677043 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-549+6689A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677043 | |||||||
| chr7:1677114 | T | C | 2 | a0006c0010t0045g0150 a0006c0010t0046g0151 |
2 | NA19003.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-549+6760T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677114 | |||||||
| chr7:1677203 | C | A | 2 | a0001c0001t0001g0290 a0001c0001t0038g0287 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-549+6849C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677203 | |||||||
| chr7:1677346 | T | C | 11 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0185 others(8): Show |
11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-549+6992T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677346 | |||||||
| chr7:1677415 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-549+7061T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677415 | |||||||
| chr7:1677478 | G | T | 3 | a0001c0001t0025g0012 a0001c0001t0065g0286 a0002c0003t0006g0013 |
3 | HG02257.hp1 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-549+7124G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677478 | |||||||
| chr7:1677554 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-549+7200G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677554 | |||||||
| chr7:1677577 | C | G | 1 | a0001c0011t0034g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-549+7223C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677577 | |||||||
| chr7:1677650 | C | T | 2 | a0001c0025t0058g0046 a0002c0003t0024g0045 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-549+7296C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677650 | |||||||
| chr7:1677686 | GCCGATGT others(8): Show |
G | 1 | a0001c0001t0001g0016 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-549+7333_-549+734 others(19): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677686 | |||||||
| chr7:1677871 | G | A | 19 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0053 others(16): Show |
19 | HG01099.hp2 HG01255.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-549+7517G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677871 | |||||||
| chr7:1677955 | A | G | 1 | a0001c0001t0005g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-549+7601A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1677955 | |||||||
| chr7:1678042 | C | A | 9 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0185 others(6): Show |
9 | HG02451.hp1 HG02622.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.-549+7688C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678042 | |||||||
| chr7:1678081 | G | T | 2 | a0001c0001t0021g0268 a0001c0004t0061g0269 |
2 | NA18959.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-549+7727G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678081 | |||||||
| chr7:1678096 | C | G | 59 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0191 others(56): Show |
59 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.-549+7742C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678096 | |||||||
| chr7:1678148 | G | A | 1 | a0001c0001t0013g0230 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-549+7794G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678148 | |||||||
| chr7:1678243 | A | C | 1 | a0001c0001t0005g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-549+7889A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678243 | |||||||
| chr7:1678355 | G | A | 2 | a0001c0025t0058g0046 a0002c0003t0024g0045 |
2 | NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-549+8001G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678355 | |||||||
| chr7:1678457 | T | C | 1 | a0002c0003t0050g0178 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-549+8103T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678457 | |||||||
| chr7:1678746 | C | T | 1 | a0001c0002t0031g0236 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-549+8392C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678746 | |||||||
| chr7:1678759 | C | T | 1 | a0001c0001t0017g0103 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-549+8405C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1678759 | |||||||
| chr7:1679085 | G | T | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-549+8731G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679085 | |||||||
| chr7:1679147 | G | A | 1 | a0002c0003t0024g0182 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-549+8793G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679147 | |||||||
| chr7:1679158 | C | T | 1 | a0001c0001t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-549+8804C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679158 | |||||||
| chr7:1679173 | ACG | A | 7 | a0001c0001t0012g0183 a0001c0001t0016g0038 a0001c0001t0025g0012 others(4): Show |
7 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-549+8825_-549+882 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1679173 | ||||||
| chr7:1679177 | G | GCA | 22 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(19): Show |
23 | HG00408.hp2 HG01106.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.-549+8824_-549+882 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1679177 | ||||||
| chr7:1679179 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(169): Show |
176 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.-549+8825G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679179 | |||||||
| chr7:1679179 | G | GCA | 19 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0053 others(16): Show |
19 | HG00639.hp2 HG01099.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-549+8842_-549+884 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1679179 | ||||||
| chr7:1679181 | A | G | 2 | a0001c0001t0047g0059 a0001c0002t0007g0058 |
2 | HG01975.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-549+8827A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679181 | |||||||
| chr7:1679297 | G | A | 1 | a0001c0001t0016g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-548-8761G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679297 | |||||||
| chr7:1679332 | G | A | 1 | a0001c0001t0015g0162 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-548-8726G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679332 | |||||||
| chr7:1679451 | G | A | 2 | a0001c0001t0003g0134 a0001c0001t0003g0135 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-548-8607G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679451 | |||||||
| chr7:1679541 | C | T | 1 | a0002c0003t0006g0013 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-548-8517C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679541 | |||||||
| chr7:1679556 | C | A | 1 | a0001c0001t0033g0276 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-548-8502C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679556 | |||||||
| chr7:1679651 | C | G | 1 | a0001c0001t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-548-8407C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679651 | |||||||
| chr7:1679685 | C | T | 11 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0185 others(8): Show |
11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-548-8373C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679685 | |||||||
| chr7:1679704 | C | T | 1 | a0002c0003t0024g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-548-8354C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679704 | |||||||
| chr7:1679726 | T | C | 3 | a0001c0001t0006g0036 a0001c0001t0016g0038 a0002c0003t0050g0178 |
3 | HG02896.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-548-8332T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679726 | |||||||
| chr7:1679753 | C | T | 1 | a0001c0001t0005g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-548-8305C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679753 | |||||||
| chr7:1679919 | G | A | 2 | a0001c0001t0012g0210 a0001c0001t0012g0211 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-548-8139G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1679919 | |||||||
| chr7:1680088 | C | T | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-548-7970C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680088 | |||||||
| chr7:1680097 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0002g0241 a0001c0001t0003g0047 others(21): Show |
25 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-548-7961G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680097 | |||||||
| chr7:1680120 | C | T | 5 | a0001c0001t0012g0183 a0001c0001t0025g0012 a0001c0001t0065g0286 others(2): Show |
5 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.-548-7938C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680120 | |||||||
| chr7:1680304 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-548-7754C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680304 | |||||||
| chr7:1680313 | C | T | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-548-7745C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680313 | |||||||
| chr7:1680616 | T | G | 41 | a0001c0001t0001g0002 a0001c0001t0001g0157 a0001c0001t0001g0159 others(38): Show |
42 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-548-7442T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680616 | |||||||
| chr7:1680618 | A | G | 4 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0027g0189 others(1): Show |
5 | NA18964.hp2 NA18995.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-548-7440A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680618 | |||||||
| chr7:1680655 | A | G | 2 | a0001c0001t0031g0102 a0005c0009t0001g0110 |
2 | HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-548-7403A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680655 | |||||||
| chr7:1680686 | C | T | 3 | a0001c0001t0006g0129 a0001c0001t0009g0122 a0001c0007t0005g0130 |
3 | HG01891.hp1 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-548-7372C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680686 | |||||||
| chr7:1680706 | C | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0238 others(58): Show |
63 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.-548-7352C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1680706 | |||||||
| chr7:1680737 | A | AT | 8 | a0001c0001t0001g0143 a0001c0001t0001g0229 a0001c0001t0001g0263 others(5): Show |
8 | HG00438.hp2 HG00621.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-548-7299dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1680737 | ||||||
| chr7:1680737 | AT | A | 28 | a0001c0001t0001g0016 a0001c0001t0001g0053 a0001c0001t0001g0065 others(25): Show |
28 | HG00140.hp2 HG01167.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.-548-7299delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1680737 | ||||||
| chr7:1681122 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-548-6936A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681122 | |||||||
| chr7:1681178 | G | T | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(289): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-548-6880G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681178 | |||||||
| chr7:1681207 | T | C | 2 | a0001c0001t0012g0183 a0002c0003t0024g0182 |
2 | HG01167.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-548-6851T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681207 | |||||||
| chr7:1681222 | G | A | 2 | a0001c0001t0002g0171 a0001c0001t0039g0172 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-548-6836G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681222 | |||||||
| chr7:1681333 | A | AG | 19 | a0001c0001t0001g0126 a0001c0001t0001g0146 a0001c0001t0001g0289 others(16): Show |
20 | HG01168.hp1 HG01169.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.-548-6723dupG | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1681333 | ||||||
| chr7:1681384 | A | G | 3 | a0001c0001t0001g0290 a0001c0001t0003g0291 a0001c0001t0038g0287 |
3 | HG02559.hp1 HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-548-6674A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681384 | |||||||
| chr7:1681694 | C | T | 4 | a0001c0001t0012g0183 a0001c0001t0025g0012 a0002c0003t0006g0013 others(1): Show |
4 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-548-6364C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681694 | |||||||
| chr7:1681744 | G | C | 2 | a0001c0001t0001g0290 a0001c0001t0003g0291 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-548-6314G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681744 | |||||||
| chr7:1681910 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-548-6148T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1681910 | |||||||
| chr7:1682266 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-548-5792A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682266 | |||||||
| chr7:1682440 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-548-5618T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682440 | |||||||
| chr7:1682561 | C | T | 15 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(12): Show |
15 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-548-5497C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682561 | |||||||
| chr7:1682574 | G | A | 1 | a0001c0001t0052g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-548-5484G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682574 | |||||||
| chr7:1682608 | AT | A | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(280): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.-548-5432delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1682608 | ||||||
| chr7:1682633 | A | G | 16 | a0001c0001t0001g0146 a0001c0001t0003g0134 a0001c0001t0003g0135 others(13): Show |
17 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.-548-5425A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682633 | |||||||
| chr7:1682916 | G | A | 2 | a0001c0001t0001g0003 a0001c0018t0001g0003 |
2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-548-5142G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1682916 | |||||||
| chr7:1683055 | T | C | 15 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(12): Show |
15 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-548-5003T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683055 | |||||||
| chr7:1683076 | T | C | 3 | a0001c0001t0065g0286 a0001c0025t0058g0046 a0002c0003t0050g0178 |
3 | HG02258.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-548-4982T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683076 | |||||||
| chr7:1683175 | C | CT | 29 | a0001c0001t0001g0002 a0001c0001t0002g0116 a0001c0001t0002g0241 others(26): Show |
30 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-548-4872dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1683175 | ||||||
| chr7:1683466 | G | C | 1 | a0001c0001t0001g0010 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-548-4592G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683466 | |||||||
| chr7:1683502 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-548-4556T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683502 | |||||||
| chr7:1683569 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-548-4489A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683569 | |||||||
| chr7:1683753 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-548-4305G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1683753 | |||||||
| chr7:1684070 | A | C | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-548-3988A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684070 | |||||||
| chr7:1684154 | A | G | 1 | a0001c0001t0006g0282 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-548-3904A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684154 | |||||||
| chr7:1684247 | C | T | 2 | a0001c0007t0005g0128 a0001c0007t0005g0184 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-548-3811C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684247 | |||||||
| chr7:1684388 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-548-3670A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684388 | |||||||
| chr7:1684454 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0002g0241 a0001c0001t0003g0047 others(25): Show |
29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-548-3604A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684454 | |||||||
| chr7:1684657 | C | T | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-548-3401C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684657 | |||||||
| chr7:1684837 | A | G | 1 | a0003c0006t0016g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-548-3221A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684837 | |||||||
| chr7:1684896 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-548-3162A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684896 | |||||||
| chr7:1684904 | A | T | 1 | a0001c0001t0005g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-548-3154A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684904 | |||||||
| chr7:1684934 | A | G | 10 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(7): Show |
10 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-548-3124A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1684934 | |||||||
| chr7:1685119 | G | C | 1 | a0001c0002t0004g0152 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-548-2939G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1685119 | |||||||
| chr7:1685221 | A | G | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-548-2837A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1685221 | |||||||
| chr7:1685312 | G | A | 1 | a0001c0001t0009g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-548-2746G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1685312 | |||||||
| chr7:1685774 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0060g0245 |
2 | NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-548-2284G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1685774 | |||||||
| chr7:1686020 | A | G | 43 | a0001c0001t0001g0002 a0001c0001t0001g0157 a0001c0001t0001g0159 others(40): Show |
44 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.-548-2038A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686020 | |||||||
| chr7:1686059 | CT | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(54): Show |
58 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-548-1989delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1686059 | ||||||
| chr7:1686097 | C | T | 8 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0055g0288 others(5): Show |
9 | HG01884.hp2 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-548-1961C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686097 | |||||||
| chr7:1686115 | T | C | 23 | a0001c0001t0001g0002 a0001c0001t0002g0241 a0001c0001t0005g0155 others(20): Show |
24 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.-548-1943T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686115 | |||||||
| chr7:1686311 | G | GT | 12 | a0001c0001t0001g0011 a0001c0001t0001g0100 a0001c0001t0001g0234 others(9): Show |
12 | HG00621.hp2 HG00738.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.-548-1728dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1686311 | ||||||
| chr7:1686313 | T | TC | 53 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(50): Show |
54 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-548-1745_-548-174 others(5): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686313 | |||||||
| chr7:1686314 | T | C | 1 | a0001c0001t0040g0048 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-548-1744T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686314 | |||||||
| chr7:1686924 | A | C | 1 | a0001c0001t0014g0099 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-548-1134A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686924 | |||||||
| chr7:1686935 | G | T | 1 | a0003c0006t0016g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-548-1123G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1686935 | |||||||
| chr7:1687135 | G | A | 4 | a0001c0001t0001g0290 a0001c0001t0003g0291 a0001c0001t0006g0039 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-548-923G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1687135 | |||||||
| chr7:1687348 | A | AT | 10 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(7): Show |
10 | HG02451.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-548-698dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1687348 | ||||||
| chr7:1687348 | AT | A | 13 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0185 others(10): Show |
13 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-548-698delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1687348 | ||||||
| chr7:1687417 | A | T | 1 | a0001c0002t0001g0242 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-548-641A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1687417 | |||||||
| chr7:1687465 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0061 |
2 | HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-548-593C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1687465 | |||||||
| chr7:1687502 | C | G | 3 | a0001c0001t0065g0286 a0001c0025t0058g0046 a0002c0003t0050g0178 |
3 | HG02258.hp1 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-548-556C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | chr7 | 1687502 | |||||||
| chr7:1688031 | A | AT | 29 | a0001c0001t0001g0023 a0001c0001t0001g0098 a0001c0001t0001g0126 others(26): Show |
30 | HG00280.hp1 HG00280.hp2 HG01168.hp1 others(27): Show |
splice_region_variant&intron_variant | LOW | c.-548-5dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1688031 | ||||||
| chr7:1688031 | AT | A | 15 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(12): Show |
15 | HG01167.hp2 HG02145.hp1 HG02451.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.-548-5delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1688031 | ||||||
| chr7:1688031 | ATTTTTTT others(1): Show |
A | 25 | a0001c0001t0001g0002 a0001c0001t0003g0047 a0001c0001t0005g0155 others(22): Show |
26 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(23): Show |
splice_region_variant&intron_variant | LOW | c.-548-12_-548-5delT others(7): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1688031 | ||||||
| chr7:1688031 | ATTTTTTT others(2): Show |
A | 16 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0003g0134 others(13): Show |
16 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.-548-13_-548-5delT others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr7 | 1688031 | ||||||
| chr7:1688352 | G | C | 3 | a0001c0001t0002g0246 a0001c0002t0003g0243 a0001c0002t0004g0270 |
3 | HG02735.hp2 HG03491.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-456+202G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1688352 | |||||||
| chr7:1688509 | G | A | 2 | a0001c0001t0065g0286 a0001c0025t0058g0046 |
2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-456+359G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1688509 | |||||||
| chr7:1688567 | C | A | 1 | a0001c0001t0005g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-456+417C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1688567 | |||||||
| chr7:1688686 | A | G | 1 | a0001c0027t0062g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-456+536A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1688686 | |||||||
| chr7:1689157 | G | A | 1 | a0003c0006t0016g0141 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-456+1007G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689157 | |||||||
| chr7:1689255 | T | C | 66 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(63): Show |
68 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-456+1105T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689255 | |||||||
| chr7:1689417 | G | A | 1 | a0001c0001t0008g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-456+1267G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689417 | |||||||
| chr7:1689448 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-456+1298C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689448 | |||||||
| chr7:1689740 | C | T | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+1590C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689740 | |||||||
| chr7:1689997 | C | T | 14 | a0001c0001t0002g0208 a0001c0001t0004g0204 a0001c0001t0004g0205 others(11): Show |
14 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.-456+1847C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1689997 | |||||||
| chr7:1690009 | A | G | 15 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(12): Show |
15 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-456+1859A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690009 | |||||||
| chr7:1690046 | T | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(43): Show |
47 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-456+1896T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690046 | |||||||
| chr7:1690060 | A | C | 3 | a0001c0001t0006g0036 a0001c0001t0016g0038 a0002c0003t0050g0178 |
3 | HG02896.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-456+1910A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690060 | |||||||
| chr7:1690065 | A | T | 15 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(12): Show |
15 | HG01167.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-456+1915A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690065 | |||||||
| chr7:1690118 | C | T | 2 | a0001c0001t0065g0286 a0001c0025t0058g0046 |
2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-456+1968C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690118 | |||||||
| chr7:1690217 | T | A | 155 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(152): Show |
159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.-456+2067T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690217 | |||||||
| chr7:1690333 | G | C | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+2183G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690333 | |||||||
| chr7:1690450 | G | C | 1 | a0001c0001t0011g0106 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-456+2300G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690450 | |||||||
| chr7:1690495 | A | G | 269 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(266): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-456+2345A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690495 | |||||||
| chr7:1690522 | G | A | 2 | a0001c0001t0006g0036 a0001c0001t0016g0038 |
2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-456+2372G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690522 | |||||||
| chr7:1690726 | C | T | 73 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(70): Show |
75 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-456+2576C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690726 | |||||||
| chr7:1690927 | T | C | 2 | a0001c0001t0006g0036 a0001c0001t0016g0038 |
2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-456+2777T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690927 | |||||||
| chr7:1690947 | G | T | 2 | a0001c0001t0005g0137 a0001c0001t0048g0125 |
2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-456+2797G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690947 | |||||||
| chr7:1690966 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-456+2816A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1690966 | |||||||
| chr7:1691049 | TAA | T | 4 | a0001c0001t0001g0290 a0001c0001t0003g0291 a0001c0001t0038g0287 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-456+2901_-456+290 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1691049 | ||||||
| chr7:1691116 | C | T | 2 | a0001c0001t0065g0286 a0001c0025t0058g0046 |
2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-456+2966C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691116 | |||||||
| chr7:1691133 | G | T | 2 | a0001c0001t0006g0036 a0001c0001t0016g0038 |
2 | HG02896.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-456+2983G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691133 | |||||||
| chr7:1691568 | T | G | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-456+3418T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691568 | |||||||
| chr7:1691637 | T | A | 1 | a0015c0023t0003g0131 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-456+3487T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691637 | |||||||
| chr7:1691651 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-456+3501C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691651 | |||||||
| chr7:1691876 | C | T | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+3726C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1691876 | |||||||
| chr7:1692044 | G | A | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+3894G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692044 | |||||||
| chr7:1692055 | G | A | 1 | a0001c0001t0043g0163 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-456+3905G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692055 | |||||||
| chr7:1692230 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0003g0047 a0001c0001t0005g0155 others(25): Show |
29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-456+4080A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692230 | |||||||
| chr7:1692300 | C | T | 6 | a0001c0001t0003g0024 a0001c0001t0003g0185 a0001c0001t0012g0148 others(3): Show |
6 | HG02145.hp2 HG02647.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-456+4150C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692300 | |||||||
| chr7:1692326 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0008g0018 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-456+4176C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692326 | |||||||
| chr7:1692374 | A | G | 62 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0238 others(59): Show |
64 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.-456+4224A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692374 | |||||||
| chr7:1692470 | C | A | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-456+4320C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692470 | |||||||
| chr7:1692491 | G | T | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+4341G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692491 | |||||||
| chr7:1692509 | A | G | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(289): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-456+4359A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692509 | |||||||
| chr7:1692811 | G | A | 1 | a0001c0001t0060g0245 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-456+4661G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1692811 | |||||||
| chr7:1693029 | A | G | 11 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0185 others(8): Show |
11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-456+4879A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693029 | |||||||
| chr7:1693306 | C | T | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-456+5156C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693306 | |||||||
| chr7:1693346 | G | A | 1 | a0001c0001t0013g0267 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-456+5196G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693346 | |||||||
| chr7:1693460 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-456+5310C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693460 | |||||||
| chr7:1693466 | G | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0238 a0001c0001t0001g0239 others(51): Show |
56 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.-456+5316G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693466 | |||||||
| chr7:1693546 | C | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0157 a0001c0001t0001g0159 others(41): Show |
45 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-456+5396C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693546 | |||||||
| chr7:1693556 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0156 others(21): Show |
25 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.-456+5406C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693556 | |||||||
| chr7:1693591 | G | T | 1 | a0001c0002t0004g0096 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-456+5441G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693591 | |||||||
| chr7:1693624 | C | T | 1 | a0001c0001t0012g0148 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-456+5474C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693624 | |||||||
| chr7:1693670 | C | T | 1 | a0001c0001t0005g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-456+5520C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693670 | |||||||
| chr7:1693788 | G | C | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-456+5638G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693788 | |||||||
| chr7:1693838 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01934.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-456+5688G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693838 | |||||||
| chr7:1693997 | C | T | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-456+5847C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1693997 | |||||||
| chr7:1694009 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+5859C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694009 | |||||||
| chr7:1694142 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+5992C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694142 | |||||||
| chr7:1694159 | T | C | 2 | a0001c0001t0012g0148 a0003c0006t0016g0181 |
2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-456+6009T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694159 | |||||||
| chr7:1694179 | C | T | 3 | a0001c0001t0007g0266 a0001c0002t0003g0265 a0001c0002t0027g0057 |
3 | HG03831.hp1 HG03927.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-456+6029C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694179 | |||||||
| chr7:1694310 | C | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0061 others(2): Show |
5 | HG00741.hp2 HG01361.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-456+6160C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694310 | |||||||
| chr7:1694370 | C | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+6220C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694370 | |||||||
| chr7:1694413 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-456+6263A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694413 | |||||||
| chr7:1694555 | G | A | 1 | a0001c0001t0014g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-456+6405G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694555 | |||||||
| chr7:1694559 | C | T | 45 | a0001c0001t0001g0002 a0001c0001t0001g0157 a0001c0001t0001g0159 others(42): Show |
46 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.-456+6409C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694559 | |||||||
| chr7:1694587 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+6437G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694587 | |||||||
| chr7:1694665 | C | T | 2 | a0001c0002t0003g0105 a0001c0002t0003g0111 |
2 | HG01516.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-456+6515C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694665 | |||||||
| chr7:1694724 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-456+6574G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694724 | |||||||
| chr7:1694868 | A | G | 19 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(16): Show |
19 | HG01167.hp2 HG02109.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-456+6718A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694868 | |||||||
| chr7:1694874 | A | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+6724A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1694874 | |||||||
| chr7:1695039 | T | C | 11 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0185 others(8): Show |
11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-456+6889T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695039 | |||||||
| chr7:1695072 | AGACGGCT others(3): Show |
A | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-456+6925_-456+693 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1695072 | ||||||
| chr7:1695076 | G | A | 11 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0185 others(8): Show |
11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-456+6926G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695076 | |||||||
| chr7:1695134 | G | C | 2 | a0001c0001t0006g0119 a0003c0006t0016g0141 |
2 | HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-456+6984G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695134 | |||||||
| chr7:1695680 | G | A | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-456+7530G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695680 | |||||||
| chr7:1695703 | G | A | 2 | a0001c0001t0012g0148 a0003c0006t0016g0181 |
2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-456+7553G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695703 | |||||||
| chr7:1695747 | C | CA | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(133): Show |
139 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-456+7622dupA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1695747 | ||||||
| chr7:1695747 | C | CAA | 66 | a0001c0001t0001g0008 a0001c0001t0001g0023 a0001c0001t0001g0027 others(63): Show |
67 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.-456+7621_-456+762 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1695747 | ||||||
| chr7:1695747 | C | CAAA | 12 | a0001c0001t0001g0030 a0001c0001t0001g0043 a0001c0001t0001g0157 others(9): Show |
12 | HG00544.hp1 HG02145.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-456+7620_-456+762 others(7): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1695747 | ||||||
| chr7:1695762 | A | C | 10 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0185 others(7): Show |
10 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-456+7612A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695762 | |||||||
| chr7:1695786 | G | T | 1 | a0001c0001t0001g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-456+7636G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695786 | |||||||
| chr7:1695836 | T | A | 11 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0003g0185 others(8): Show |
11 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-456+7686T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695836 | |||||||
| chr7:1695919 | C | T | 1 | a0001c0001t0005g0218 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-456+7769C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695919 | |||||||
| chr7:1695970 | C | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(69): Show |
74 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-456+7820C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695970 | |||||||
| chr7:1695977 | C | T | 1 | a0001c0002t0003g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-456+7827C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1695977 | |||||||
| chr7:1696015 | C | T | 1 | a0001c0002t0004g0152 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-456+7865C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696015 | |||||||
| chr7:1696146 | G | A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0203 others(31): Show |
34 | HG00423.hp2 HG00438.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.-456+7996G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696146 | |||||||
| chr7:1696160 | C | CAG | 9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0006g0036 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-456+8025_-456+802 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696160 | ||||||
| chr7:1696175 | A | AGT | 16 | a0001c0001t0001g0026 a0001c0001t0003g0047 a0001c0001t0003g0134 others(13): Show |
16 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-456+8043_-456+804 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696175 | ||||||
| chr7:1696175 | A | AGTGTGTG others(3): Show |
3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8035_-456+804 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696175 | ||||||
| chr7:1696175 | A | T | 1 | a0001c0004t0034g0127 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-456+8025A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696175 | |||||||
| chr7:1696191 | T | C | 1 | a0001c0027t0062g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-456+8041T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696191 | |||||||
| chr7:1696195 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8045C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696195 | |||||||
| chr7:1696219 | A | C | 23 | a0001c0001t0001g0002 a0001c0001t0006g0282 a0001c0001t0007g0164 others(20): Show |
24 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.-456+8069A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696219 | |||||||
| chr7:1696266 | G | C | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+8116G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696266 | |||||||
| chr7:1696277 | G | GGA | 4 | a0001c0001t0001g0289 a0001c0001t0035g0281 a0001c0001t0055g0288 others(1): Show |
4 | HG02280.hp2 NA19003.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-456+8145_-456+814 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696277 | ||||||
| chr7:1696277 | GGAGA | G | 16 | a0001c0001t0001g0026 a0001c0001t0001g0157 a0001c0001t0001g0159 others(13): Show |
16 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.-456+8143_-456+814 others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696277 | ||||||
| chr7:1696352 | G | C | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+8202G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696352 | |||||||
| chr7:1696367 | G | A | 2 | a0001c0001t0006g0282 a0001c0001t0035g0281 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-456+8217G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696367 | |||||||
| chr7:1696392 | C | CT | 7 | a0001c0001t0001g0079 a0001c0001t0002g0073 a0001c0001t0002g0116 others(4): Show |
7 | HG00423.hp2 HG02145.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-456+8258dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1696392 | ||||||
| chr7:1696514 | C | A | 1 | a0001c0001t0047g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-456+8364C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696514 | |||||||
| chr7:1696562 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8412C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696562 | |||||||
| chr7:1696613 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8463G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696613 | |||||||
| chr7:1696665 | G | C | 3 | a0001c0001t0001g0253 a0001c0001t0001g0274 a0001c0001t0060g0245 |
3 | HG02135.hp1 HG02165.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.-456+8515G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696665 | |||||||
| chr7:1696735 | C | G | 4 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0002c0003t0050g0178 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-456+8585C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696735 | |||||||
| chr7:1696736 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8586G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696736 | |||||||
| chr7:1696766 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8616T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696766 | |||||||
| chr7:1696785 | A | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8635A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696785 | |||||||
| chr7:1696809 | G | A | 13 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(10): Show |
13 | HG01243.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-456+8659G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696809 | |||||||
| chr7:1696846 | T | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+8696T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1696846 | |||||||
| chr7:1697022 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(41): Show |
45 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-456+8872G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697022 | |||||||
| chr7:1697043 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-456+8893C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697043 | |||||||
| chr7:1697048 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-456+8898G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697048 | |||||||
| chr7:1697052 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-456+8902C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697052 | |||||||
| chr7:1697269 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+9119C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697269 | |||||||
| chr7:1697293 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-456+9143C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697293 | |||||||
| chr7:1697422 | A | C | 1 | a0001c0001t0001g0027 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-456+9272A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697422 | |||||||
| chr7:1697456 | G | C | 9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0006g0036 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-456+9306G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697456 | |||||||
| chr7:1697489 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0143 |
2 | HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-456+9339C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697489 | |||||||
| chr7:1697490 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-456+9340G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697490 | |||||||
| chr7:1697568 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-456+9418C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697568 | |||||||
| chr7:1697576 | C | T | 12 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0006g0036 others(9): Show |
13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-456+9426C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697576 | |||||||
| chr7:1697733 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-456+9583C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697733 | |||||||
| chr7:1697766 | C | T | 1 | a0001c0001t0017g0103 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-456+9616C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697766 | |||||||
| chr7:1697849 | A | G | 2 | a0001c0001t0002g0077 a0001c0001t0014g0078 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-456+9699A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697849 | |||||||
| chr7:1697860 | C | T | 2 | a0004c0008t0028g0284 a0004c0008t0029g0283 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-456+9710C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697860 | |||||||
| chr7:1697861 | G | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(55): Show |
60 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-456+9711G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697861 | |||||||
| chr7:1697947 | G | A | 1 | a0001c0001t0048g0125 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-456+9797G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697947 | |||||||
| chr7:1697982 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-456+9832C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1697982 | |||||||
| chr7:1698180 | A | G | 15 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0159 others(12): Show |
16 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-456+10030A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698180 | |||||||
| chr7:1698231 | T | A | 28 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(25): Show |
29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-456+10081T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698231 | |||||||
| chr7:1698274 | T | C | 1 | a0001c0002t0053g0118 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-456+10124T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698274 | |||||||
| chr7:1698459 | C | T | 1 | a0002c0003t0003g0022 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-456+10309C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698459 | |||||||
| chr7:1698491 | A | G | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-456+10341A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698491 | |||||||
| chr7:1698737 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-455-10354T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1698737 | |||||||
| chr7:1699048 | A | G | 1 | a0001c0001t0002g0197 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-455-10043A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699048 | |||||||
| chr7:1699295 | A | G | 1 | a0001c0001t0038g0287 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-455-9796A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699295 | |||||||
| chr7:1699714 | T | C | 3 | a0001c0001t0001g0290 a0001c0001t0003g0291 a0002c0024t0030g0028 |
3 | HG02559.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-455-9377T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699714 | |||||||
| chr7:1699738 | C | T | 2 | a0001c0001t0025g0012 a0001c0001t0038g0287 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-455-9353C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699738 | |||||||
| chr7:1699828 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-455-9263C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699828 | |||||||
| chr7:1699849 | G | A | 4 | a0001c0001t0003g0047 a0001c0001t0005g0149 a0001c0001t0006g0036 others(1): Show |
4 | HG01109.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-9242G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699849 | |||||||
| chr7:1699930 | G | C | 29 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(26): Show |
30 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-455-9161G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1699930 | |||||||
| chr7:1700193 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(24): Show |
28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-455-8898C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700193 | |||||||
| chr7:1700223 | G | A | 27 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(24): Show |
28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-455-8868G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700223 | |||||||
| chr7:1700253 | AC | A | 27 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(24): Show |
28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-455-8836delC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1700253 | ||||||
| chr7:1700280 | A | G | 27 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(24): Show |
28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-455-8811A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700280 | |||||||
| chr7:1700298 | A | G | 27 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(24): Show |
28 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.-455-8793A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700298 | |||||||
| chr7:1700326 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-455-8765C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700326 | |||||||
| chr7:1700449 | C | A | 2 | a0001c0001t0012g0210 a0001c0001t0012g0211 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-455-8642C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700449 | |||||||
| chr7:1700488 | C | G | 28 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(25): Show |
29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-455-8603C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700488 | |||||||
| chr7:1700505 | G | A | 1 | a0001c0001t0044g0217 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-455-8586G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700505 | |||||||
| chr7:1700635 | C | T | 1 | a0003c0006t0016g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-455-8456C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700635 | |||||||
| chr7:1700726 | G | A | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-455-8365G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700726 | |||||||
| chr7:1700739 | C | T | 49 | a0001c0001t0001g0016 a0001c0001t0001g0244 a0001c0001t0001g0251 others(46): Show |
50 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.-455-8352C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700739 | |||||||
| chr7:1700746 | C | T | 1 | a0001c0002t0027g0057 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-455-8345C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700746 | |||||||
| chr7:1700767 | C | G | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-8324C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700767 | |||||||
| chr7:1700793 | T | G | 11 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-455-8298T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700793 | |||||||
| chr7:1700797 | C | T | 3 | a0001c0001t0005g0149 a0001c0001t0006g0036 a0001c0026t0057g0186 |
3 | HG01123.hp1 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-8294C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700797 | |||||||
| chr7:1700827 | C | G | 29 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(26): Show |
30 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-455-8264C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700827 | |||||||
| chr7:1700893 | G | A | 2 | a0004c0008t0028g0284 a0004c0008t0029g0283 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-455-8198G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700893 | |||||||
| chr7:1700895 | C | A | 1 | a0001c0001t0001g0244 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-455-8196C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1700895 | |||||||
| chr7:1701063 | G | T | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-455-8028G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701063 | |||||||
| chr7:1701071 | ATGTGTGC others(17): Show |
A | 2 | a0001c0001t0012g0210 a0001c0001t0012g0211 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-455-8011_-455-798 others(28): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1701071 | ||||||
| chr7:1701092 | C | T | 3 | a0001c0001t0001g0002 a0001c0002t0003g0105 a0001c0002t0003g0111 |
4 | HG01516.hp1 HG01934.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-7999C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701092 | |||||||
| chr7:1701107 | A | G | 28 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(25): Show |
29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-455-7984A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701107 | |||||||
| chr7:1701111 | G | A | 2 | a0001c0001t0025g0012 a0001c0001t0038g0287 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-455-7980G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701111 | |||||||
| chr7:1701135 | ATG | A | 3 | a0001c0001t0005g0285 a0001c0001t0012g0183 a0002c0003t0024g0182 |
3 | HG01167.hp2 HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-455-7945_-455-794 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1701135 | ||||||
| chr7:1701154 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-455-7937G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701154 | |||||||
| chr7:1701334 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(25): Show |
29 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.-455-7757C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701334 | |||||||
| chr7:1701378 | G | C | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-7713G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701378 | |||||||
| chr7:1701689 | C | T | 2 | a0001c0001t0025g0012 a0001c0001t0038g0287 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-455-7402C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701689 | |||||||
| chr7:1701787 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-455-7304A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701787 | |||||||
| chr7:1701877 | T | A | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-7214T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701877 | |||||||
| chr7:1701990 | T | C | 13 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(10): Show |
14 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-455-7101T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1701990 | |||||||
| chr7:1702121 | T | G | 1 | a0001c0001t0005g0155 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-455-6970T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702121 | |||||||
| chr7:1702177 | C | T | 1 | a0001c0002t0003g0214 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-455-6914C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702177 | |||||||
| chr7:1702220 | T | C | 1 | a0001c0001t0028g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-455-6871T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702220 | |||||||
| chr7:1702371 | C | T | 1 | a0001c0001t0012g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-455-6720C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702371 | |||||||
| chr7:1702394 | T | G | 9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6697T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702394 | |||||||
| chr7:1702401 | C | T | 1 | a0001c0001t0019g0123 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-455-6690C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702401 | |||||||
| chr7:1702408 | A | G | 9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6683A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702408 | |||||||
| chr7:1702410 | G | A | 15 | a0001c0001t0001g0023 a0001c0001t0001g0053 a0001c0001t0001g0143 others(12): Show |
15 | HG01255.hp1 HG02055.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-455-6681G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702410 | |||||||
| chr7:1702418 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-455-6673G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702418 | |||||||
| chr7:1702421 | G | T | 2 | a0001c0001t0006g0036 a0001c0005t0010g0004 |
3 | HG02630.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-6670G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702421 | |||||||
| chr7:1702422 | G | C | 2 | a0001c0001t0006g0036 a0001c0005t0010g0004 |
3 | HG02630.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-6669G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702422 | |||||||
| chr7:1702423 | G | A | 2 | a0001c0001t0006g0036 a0001c0005t0010g0004 |
3 | HG02630.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-6668G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702423 | |||||||
| chr7:1702424 | G | A | 2 | a0001c0001t0006g0036 a0001c0005t0010g0004 |
3 | HG02630.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-6667G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702424 | |||||||
| chr7:1702424 | G | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0289 |
2 | NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-455-6667G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702424 | |||||||
| chr7:1702425 | G | A | 2 | a0001c0001t0006g0036 a0001c0005t0010g0004 |
3 | HG02630.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-455-6666G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702425 | |||||||
| chr7:1702425 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0289 |
2 | NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-455-6666G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702425 | |||||||
| chr7:1702425 | G | T | 4 | a0001c0001t0055g0288 a0001c0005t0010g0144 a0001c0005t0010g0147 others(1): Show |
4 | HG02280.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-6666G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702425 | |||||||
| chr7:1702426 | G | A | 4 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0006g0036 others(1): Show |
5 | HG02630.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-455-6665G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702426 | |||||||
| chr7:1702426 | G | C | 4 | a0001c0001t0055g0288 a0001c0005t0010g0144 a0001c0005t0010g0147 others(1): Show |
4 | HG02280.hp2 HG03098.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-6665G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702426 | |||||||
| chr7:1702426 | G | T | 1 | a0001c0001t0005g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-455-6665G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702426 | |||||||
| chr7:1702427 | G | A | 12 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0006g0036 others(9): Show |
13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-455-6664G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702427 | |||||||
| chr7:1702427 | G | C | 1 | a0001c0001t0005g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-455-6664G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702427 | |||||||
| chr7:1702427 | GA | G | 22 | a0001c0001t0001g0023 a0001c0001t0001g0053 a0001c0001t0001g0143 others(19): Show |
22 | HG01109.hp2 HG01255.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-455-6653delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1702427 | ||||||
| chr7:1702439 | G | A | 9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6652G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702439 | |||||||
| chr7:1702442 | G | A | 9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6649G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702442 | |||||||
| chr7:1702444 | AGACCCTC others(87): Show |
A | 3 | a0001c0001t0005g0149 a0001c0001t0006g0036 a0001c0005t0010g0004 |
4 | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-455-6646_-455-655 others(98): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702444 | |||||||
| chr7:1702445 | G | A | 6 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0055g0288 others(3): Show |
6 | HG02280.hp2 HG03098.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-455-6646G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702445 | |||||||
| chr7:1702446 | ACCCTCCC others(85): Show |
A | 6 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0055g0288 others(3): Show |
6 | HG02280.hp2 HG03098.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-455-6644_-455-655 others(96): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702446 | |||||||
| chr7:1702540 | C | A | 9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6551C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702540 | |||||||
| chr7:1702546 | G | A | 9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-6545G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702546 | |||||||
| chr7:1702554 | ATGGATTG others(391): Show |
A | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-455-6535_-455-613 others(4): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1702554 | ||||||
| chr7:1702554 | ATGGATTG others(392): Show |
A | 8 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(5): Show |
9 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-455-6536_-455-613 others(4): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702554 | |||||||
| chr7:1702607 | C | G | 4 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0002c0003t0050g0178 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-6484C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702607 | |||||||
| chr7:1702613 | A | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0238 others(36): Show |
41 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.-455-6478A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702613 | |||||||
| chr7:1702739 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0079 |
2 | NA18967.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.-455-6352G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702739 | |||||||
| chr7:1702744 | T | G | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-6347T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702744 | |||||||
| chr7:1702921 | G | A | 1 | a0001c0001t0029g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-455-6170G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702921 | |||||||
| chr7:1702953 | T | A | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-455-6138T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1702953 | |||||||
| chr7:1703016 | C | T | 2 | a0001c0001t0012g0148 a0001c0002t0004g0280 |
2 | HG02145.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-455-6075C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703016 | |||||||
| chr7:1703055 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0238 others(41): Show |
46 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.-455-6036T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703055 | |||||||
| chr7:1703258 | C | T | 1 | a0003c0006t0016g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-455-5833C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703258 | |||||||
| chr7:1703278 | G | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0238 others(35): Show |
40 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.-455-5813G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703278 | |||||||
| chr7:1703305 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-455-5786G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703305 | |||||||
| chr7:1703385 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-455-5706G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703385 | |||||||
| chr7:1703581 | C | G | 6 | a0001c0001t0002g0073 a0001c0001t0002g0077 a0001c0001t0014g0075 others(3): Show |
6 | HG00738.hp1 HG01071.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.-455-5510C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703581 | |||||||
| chr7:1703696 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0146 others(59): Show |
65 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.-455-5395T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703696 | |||||||
| chr7:1703788 | G | A | 4 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0002c0003t0050g0178 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-5303G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703788 | |||||||
| chr7:1703815 | C | A | 3 | a0001c0001t0001g0290 a0001c0001t0003g0291 a0002c0024t0030g0028 |
3 | HG02559.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-455-5276C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703815 | |||||||
| chr7:1703846 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-455-5245T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1703846 | |||||||
| chr7:1704139 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-455-4952C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704139 | |||||||
| chr7:1704146 | G | A | 1 | a0001c0011t0034g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-455-4945G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704146 | |||||||
| chr7:1704241 | G | A | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-4850G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704241 | |||||||
| chr7:1704272 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0002g0241 |
2 | HG01192.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-455-4819G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704272 | |||||||
| chr7:1704383 | A | T | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-4708A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704383 | |||||||
| chr7:1704544 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-455-4547C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704544 | |||||||
| chr7:1704578 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-455-4513G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704578 | |||||||
| chr7:1704657 | G | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(47): Show |
51 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-455-4434G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704657 | |||||||
| chr7:1704701 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-455-4390C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704701 | |||||||
| chr7:1704757 | A | T | 4 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0002c0003t0050g0178 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-4334A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704757 | |||||||
| chr7:1704784 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0003g0291 a0002c0024t0030g0028 |
3 | HG02559.hp1 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-455-4307C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704784 | |||||||
| chr7:1704785 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(26): Show |
30 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.-455-4306G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704785 | |||||||
| chr7:1704822 | G | T | 1 | a0001c0001t0007g0167 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-455-4269G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704822 | |||||||
| chr7:1704844 | A | C | 12 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(9): Show |
12 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-455-4247A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704844 | |||||||
| chr7:1704879 | G | A | 1 | a0001c0004t0054g0168 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-455-4212G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704879 | |||||||
| chr7:1704937 | G | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(44): Show |
48 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-455-4154G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1704937 | |||||||
| chr7:1705410 | G | A | 1 | a0001c0001t0064g0014 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-455-3681G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705410 | |||||||
| chr7:1705461 | C | A | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-3630C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705461 | |||||||
| chr7:1705799 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0003g0291 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-455-3292G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705799 | |||||||
| chr7:1705813 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-455-3278C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705813 | |||||||
| chr7:1705893 | C | T | 1 | a0001c0001t0013g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-455-3198C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705893 | |||||||
| chr7:1705921 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-455-3170C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1705921 | |||||||
| chr7:1706049 | G | A | 1 | a0001c0001t0019g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-455-3042G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706049 | |||||||
| chr7:1706143 | G | C | 1 | a0001c0002t0027g0189 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-455-2948G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706143 | |||||||
| chr7:1706163 | G | A | 3 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0003c0006t0016g0181 |
3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-455-2928G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706163 | |||||||
| chr7:1706191 | G | A | 1 | a0009c0015t0032g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-455-2900G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706191 | |||||||
| chr7:1706334 | A | G | 1 | a0002c0024t0030g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-455-2757A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706334 | |||||||
| chr7:1706424 | A | AAAAAC | 5 | a0001c0001t0001g0115 a0001c0001t0001g0258 a0001c0001t0002g0173 others(2): Show |
5 | HG00738.hp2 HG00741.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-455-2625_-455-262 others(9): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | ||||||
| chr7:1706424 | A | AAAAACAA others(3): Show |
1 | a0001c0001t0031g0102 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-455-2630_-455-262 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | ||||||
| chr7:1706424 | AAAAAC | A | 92 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0027 others(89): Show |
93 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-455-2625_-455-262 others(9): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | ||||||
| chr7:1706424 | AAAAACAA others(3): Show |
A | 14 | a0001c0001t0001g0146 a0001c0001t0001g0157 a0001c0001t0001g0159 others(11): Show |
15 | HG02280.hp2 HG02630.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-455-2630_-455-262 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | ||||||
| chr7:1706424 | AAAAACAA others(8): Show |
A | 2 | a0001c0001t0003g0047 a0001c0025t0058g0046 |
2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-455-2635_-455-262 others(19): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | ||||||
| chr7:1706424 | AAAAACAA others(13): Show |
A | 4 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0002c0003t0024g0145 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-2640_-455-262 others(24): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1706424 | ||||||
| chr7:1706469 | C | A | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-455-2622C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706469 | |||||||
| chr7:1706496 | T | C | 124 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0027 others(121): Show |
126 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-455-2595T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706496 | |||||||
| chr7:1706549 | C | T | 1 | a0001c0001t0005g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-455-2542C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706549 | |||||||
| chr7:1706713 | A | G | 15 | a0001c0001t0001g0126 a0001c0001t0005g0285 a0001c0001t0006g0129 others(12): Show |
15 | HG01099.hp2 HG01167.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.-455-2378A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706713 | |||||||
| chr7:1706820 | C | T | 3 | a0001c0001t0005g0155 a0001c0001t0006g0156 a0002c0003t0006g0013 |
3 | HG01243.hp1 HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-455-2271C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706820 | |||||||
| chr7:1706903 | T | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-455-2188T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1706903 | |||||||
| chr7:1707005 | C | CAACACAC others(20): Show |
1 | a0009c0015t0032g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-455-2085_-455-205 others(31): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1707005 | ||||||
| chr7:1707073 | C | T | 3 | a0001c0001t0005g0285 a0001c0001t0012g0183 a0002c0003t0024g0182 |
3 | HG01167.hp2 HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-455-2018C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707073 | |||||||
| chr7:1707077 | G | A | 1 | a0002c0024t0030g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-455-2014G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707077 | |||||||
| chr7:1707186 | C | T | 1 | a0001c0001t0015g0162 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-455-1905C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707186 | |||||||
| chr7:1707273 | C | T | 2 | a0001c0001t0021g0268 a0001c0004t0061g0269 |
2 | NA18959.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.-455-1818C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707273 | |||||||
| chr7:1707293 | A | C | 1 | a0001c0001t0016g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-455-1798A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707293 | |||||||
| chr7:1707501 | G | A | 9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-455-1590G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707501 | |||||||
| chr7:1707550 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0157 a0001c0001t0001g0159 others(31): Show |
35 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-455-1541G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707550 | |||||||
| chr7:1707569 | C | A | 31 | a0001c0001t0001g0002 a0001c0001t0005g0155 a0001c0001t0006g0119 others(28): Show |
32 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-455-1522C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707569 | |||||||
| chr7:1707595 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-455-1496A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707595 | |||||||
| chr7:1707688 | C | T | 2 | a0001c0001t0001g0290 a0001c0001t0003g0291 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-455-1403C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707688 | |||||||
| chr7:1707975 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-455-1116C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1707975 | |||||||
| chr7:1708026 | C | G | 81 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0023 others(78): Show |
83 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-455-1065C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708026 | |||||||
| chr7:1708055 | A | AC | 12 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(9): Show |
13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-455-1030dupC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1708055 | ||||||
| chr7:1708136 | C | T | 3 | a0001c0001t0005g0285 a0001c0001t0012g0183 a0002c0003t0024g0182 |
3 | HG01167.hp2 HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-455-955C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708136 | |||||||
| chr7:1708161 | GC | G | 3 | a0001c0001t0005g0285 a0001c0001t0012g0183 a0002c0003t0024g0182 |
3 | HG01167.hp2 HG02055.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-455-929delC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708161 | |||||||
| chr7:1708167 | C | G | 2 | a0001c0001t0017g0101 a0001c0001t0059g0085 |
2 | HG01433.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-455-924C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708167 | |||||||
| chr7:1708262 | C | T | 1 | a0001c0001t0007g0166 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-455-829C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708262 | |||||||
| chr7:1708335 | G | A | 32 | a0001c0001t0001g0002 a0001c0001t0003g0047 a0001c0001t0005g0155 others(29): Show |
33 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.-455-756G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708335 | |||||||
| chr7:1708370 | A | T | 11 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-455-721A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708370 | |||||||
| chr7:1708389 | G | A | 2 | a0001c0001t0002g0171 a0001c0001t0039g0172 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-455-702G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708389 | |||||||
| chr7:1708518 | A | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0027 others(71): Show |
77 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-455-573A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708518 | |||||||
| chr7:1708697 | CAGCCCCA others(16): Show |
C | 3 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0003c0006t0016g0181 |
3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-455-384_-455-362d others(25): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr7 | 1708697 | ||||||
| chr7:1708709 | CTCTGGGG others(16): Show |
C | 4 | a0001c0001t0012g0021 a0001c0001t0025g0012 a0001c0001t0038g0287 others(1): Show |
4 | HG00639.hp2 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-455-381_-455-359d others(25): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708709 | |||||||
| chr7:1708785 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-455-306G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708785 | |||||||
| chr7:1708790 | G | A | 1 | a0001c0001t0011g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-455-301G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708790 | |||||||
| chr7:1708842 | A | G | 12 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(9): Show |
13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-455-249A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708842 | |||||||
| chr7:1708915 | T | C | 11 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-455-176T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708915 | |||||||
| chr7:1708929 | C | G | 2 | a0001c0001t0016g0038 a0011c0013t0020g0093 |
2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-455-162C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1708929 | |||||||
| chr7:1709069 | C | G | 2 | a0001c0001t0026g0020 a0001c0001t0051g0019 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-455-22C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 2/3 | chr7 | 1709069 | |||||||
| chr7:1709284 | G | A | 1 | a0003c0006t0016g0181 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-294+32G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709284 | |||||||
| chr7:1709303 | G | A | 1 | a0001c0007t0005g0184 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-294+51G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709303 | |||||||
| chr7:1709389 | G | A | 2 | a0001c0001t0025g0012 a0001c0001t0038g0287 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-294+137G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709389 | |||||||
| chr7:1709415 | A | G | 1 | a0001c0001t0025g0012 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-294+163A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709415 | |||||||
| chr7:1709506 | G | A | 2 | a0001c0001t0043g0163 a0001c0001t0044g0217 |
2 | NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-294+254G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709506 | |||||||
| chr7:1709680 | C | T | 1 | a0001c0002t0003g0188 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-294+428C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709680 | |||||||
| chr7:1709696 | C | T | 3 | a0001c0001t0019g0064 a0001c0001t0031g0102 a0005c0009t0001g0110 |
3 | HG03491.hp2 HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-294+444C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709696 | |||||||
| chr7:1709807 | A | G | 11 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+555A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709807 | |||||||
| chr7:1709963 | C | G | 2 | a0001c0001t0006g0282 a0001c0001t0035g0281 |
2 | NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-294+711C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1709963 | |||||||
| chr7:1710014 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-294+762G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710014 | |||||||
| chr7:1710219 | G | A | 11 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+967G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710219 | |||||||
| chr7:1710386 | T | C | 1 | a0001c0001t0019g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-294+1134T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710386 | |||||||
| chr7:1710510 | C | A | 1 | a0001c0001t0002g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-294+1258C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710510 | |||||||
| chr7:1710542 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0003g0047 a0001c0001t0005g0155 others(28): Show |
32 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-294+1290C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710542 | |||||||
| chr7:1710629 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(59): Show |
64 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-294+1377G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710629 | |||||||
| chr7:1710712 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-294+1460C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710712 | |||||||
| chr7:1710891 | A | G | 1 | a0001c0001t0011g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-294+1639A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710891 | |||||||
| chr7:1710918 | G | A | 1 | a0002c0024t0030g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-294+1666G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1710918 | |||||||
| chr7:1711024 | C | T | 1 | a0001c0001t0005g0149 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-294+1772C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711024 | |||||||
| chr7:1711068 | T | A | 1 | a0001c0001t0059g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-294+1816T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711068 | |||||||
| chr7:1711117 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-294+1865C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711117 | |||||||
| chr7:1711161 | C | T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0027 others(53): Show |
58 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-294+1909C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711161 | |||||||
| chr7:1711492 | T | C | 1 | a0001c0001t0002g0222 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-294+2240T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711492 | |||||||
| chr7:1711575 | T | TGA | 9 | a0001c0001t0001g0108 a0001c0001t0002g0001 a0001c0001t0002g0066 others(6): Show |
9 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.-294+2374_-294+237 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | T | TGAGA | 10 | a0001c0001t0001g0087 a0001c0001t0007g0166 a0001c0001t0007g0167 others(7): Show |
10 | HG00735.hp1 HG01255.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.-294+2372_-294+237 others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | T | TGAGAGAG others(3): Show |
1 | a0001c0002t0018g0041 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-294+2366_-294+237 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | TGA | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0027 others(50): Show |
53 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-294+2374_-294+237 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | TGAGA | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0037 others(48): Show |
51 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.-294+2372_-294+237 others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | TGAGAGA | T | 45 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(42): Show |
45 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.-294+2370_-294+237 others(10): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | TGAGAGAG others(1): Show |
T | 55 | a0001c0001t0001g0005 a0001c0001t0001g0042 a0001c0001t0001g0043 others(52): Show |
55 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.-294+2368_-294+237 others(12): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | TGAGAGAG others(3): Show |
T | 18 | a0001c0001t0001g0016 a0001c0001t0002g0073 a0001c0001t0002g0077 others(15): Show |
18 | HG01071.hp1 HG01515.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.-294+2366_-294+237 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | TGAGAGAG others(5): Show |
T | 13 | a0001c0001t0001g0023 a0001c0001t0001g0070 a0001c0001t0001g0074 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-294+2364_-294+237 others(16): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | TGAGAGAG others(7): Show |
T | 3 | a0001c0001t0001g0176 a0001c0001t0022g0076 a0001c0002t0004g0260 |
3 | HG01074.hp2 HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-294+2362_-294+237 others(18): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | TGAGAGAG others(9): Show |
T | 3 | a0001c0001t0002g0116 a0001c0002t0018g0228 a0008c0019t0001g0257 |
3 | HG01070.hp1 HG02074.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-294+2360_-294+237 others(20): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711575 | TGAGAGAG others(15): Show |
T | 2 | a0001c0001t0001g0254 a0002c0024t0030g0028 |
2 | HG00639.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-294+2354_-294+237 others(26): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1711575 | ||||||
| chr7:1711615 | A | C | 3 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0003c0006t0016g0181 |
3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+2363A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711615 | |||||||
| chr7:1711617 | A | C | 3 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0003c0006t0016g0181 |
3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+2365A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711617 | |||||||
| chr7:1711618 | GAGAGAGA others(3): Show |
G | 1 | a0001c0001t0001g0114 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-294+2367_-294+237 others(14): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711618 | |||||||
| chr7:1711619 | A | G | 11 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+2367A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711619 | |||||||
| chr7:1711658 | C | T | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-294+2406C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711658 | |||||||
| chr7:1711699 | T | C | 12 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(9): Show |
13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-294+2447T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711699 | |||||||
| chr7:1711858 | G | C | 11 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+2606G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1711858 | |||||||
| chr7:1712063 | G | A | 1 | a0001c0001t0011g0104 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-294+2811G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712063 | |||||||
| chr7:1712146 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+2894G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712146 | |||||||
| chr7:1712261 | A | G | 53 | a0001c0001t0001g0016 a0001c0001t0001g0229 a0001c0001t0001g0244 others(50): Show |
54 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-294+3009A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712261 | |||||||
| chr7:1712372 | G | A | 12 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(9): Show |
13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-294+3120G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712372 | |||||||
| chr7:1712408 | C | T | 68 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0053 others(65): Show |
69 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-294+3156C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712408 | |||||||
| chr7:1712427 | CT | C | 59 | a0001c0001t0001g0016 a0001c0001t0001g0229 a0001c0001t0001g0244 others(56): Show |
60 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-294+3186delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1712427 | ||||||
| chr7:1712477 | G | A | 1 | a0001c0001t0028g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-294+3225G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712477 | |||||||
| chr7:1712640 | C | T | 3 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0003c0006t0016g0181 |
3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+3388C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712640 | |||||||
| chr7:1712651 | C | CA | 12 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(9): Show |
13 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-294+3402dupA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1712651 | ||||||
| chr7:1712706 | A | G | 2 | a0001c0001t0012g0183 a0002c0003t0024g0182 |
2 | HG01167.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-294+3454A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712706 | |||||||
| chr7:1712711 | T | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0238 others(38): Show |
43 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.-294+3459T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712711 | |||||||
| chr7:1712812 | T | A | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-294+3560T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712812 | |||||||
| chr7:1712827 | T | G | 14 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(11): Show |
14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+3575T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1712827 | |||||||
| chr7:1713108 | C | T | 1 | a0001c0001t0016g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-294+3856C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713108 | |||||||
| chr7:1713280 | G | A | 1 | a0001c0027t0062g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-294+4028G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713280 | |||||||
| chr7:1713401 | G | A | 1 | a0001c0001t0016g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-294+4149G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713401 | |||||||
| chr7:1713447 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0157 others(39): Show |
44 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.-294+4195C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713447 | |||||||
| chr7:1713605 | C | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0030 others(61): Show |
66 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-294+4353C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713605 | |||||||
| chr7:1713679 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-294+4427C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713679 | |||||||
| chr7:1713752 | G | T | 13 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0012g0148 others(10): Show |
14 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-294+4500G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713752 | |||||||
| chr7:1713753 | G | T | 1 | a0001c0011t0034g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-294+4501G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713753 | |||||||
| chr7:1713754 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0157 a0001c0001t0001g0159 others(33): Show |
37 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.-294+4502G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713754 | |||||||
| chr7:1713831 | C | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0061 others(9): Show |
13 | HG00140.hp2 HG00544.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.-294+4579C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713831 | |||||||
| chr7:1713850 | C | T | 2 | a0001c0001t0026g0020 a0001c0001t0051g0019 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-294+4598C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713850 | |||||||
| chr7:1713876 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-294+4624C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713876 | |||||||
| chr7:1713963 | C | T | 16 | a0001c0001t0001g0026 a0001c0001t0001g0290 a0001c0001t0003g0134 others(13): Show |
16 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-294+4711C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1713963 | |||||||
| chr7:1714038 | T | C | 291 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(288): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.-294+4786T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714038 | |||||||
| chr7:1714090 | C | T | 22 | a0001c0001t0001g0203 a0001c0001t0001g0213 a0001c0001t0001g0215 others(19): Show |
22 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.-294+4838C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714090 | |||||||
| chr7:1714308 | G | A | 34 | a0001c0001t0001g0002 a0001c0001t0001g0157 a0001c0001t0001g0159 others(31): Show |
35 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-294+5056G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714308 | |||||||
| chr7:1714392 | C | A | 1 | a0001c0001t0025g0012 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-294+5140C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714392 | |||||||
| chr7:1714480 | A | G | 15 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(12): Show |
16 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.-294+5228A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714480 | |||||||
| chr7:1714482 | A | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(84): Show |
90 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-294+5230A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714482 | |||||||
| chr7:1714632 | C | G | 3 | a0001c0001t0025g0012 a0001c0001t0038g0287 a0002c0024t0030g0028 |
3 | HG02818.hp2 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-294+5380C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714632 | |||||||
| chr7:1714778 | C | A | 2 | a0001c0001t0012g0148 a0003c0006t0016g0181 |
2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+5526C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714778 | |||||||
| chr7:1714818 | C | G | 1 | a0001c0001t0006g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-294+5566C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714818 | |||||||
| chr7:1714845 | G | A | 1 | a0001c0002t0018g0228 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-294+5593G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714845 | |||||||
| chr7:1714864 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-294+5612C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714864 | |||||||
| chr7:1714872 | C | T | 14 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(11): Show |
14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+5620C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714872 | |||||||
| chr7:1714873 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(180): Show |
187 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.-294+5621A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714873 | |||||||
| chr7:1714875 | C | T | 5 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0258 others(2): Show |
5 | HG00741.hp1 HG01109.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.-294+5623C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714875 | |||||||
| chr7:1714894 | C | A | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-294+5642C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714894 | |||||||
| chr7:1714905 | G | A | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-294+5653G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714905 | |||||||
| chr7:1714907 | T | C | 3 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0003c0006t0016g0181 |
3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+5655T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714907 | |||||||
| chr7:1714917 | T | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(83): Show |
89 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.-294+5665T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1714917 | |||||||
| chr7:1715189 | C | A | 1 | a0001c0002t0004g0270 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-294+5937C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715189 | |||||||
| chr7:1715480 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0005g0161 a0001c0001t0006g0039 others(1): Show |
4 | HG01081.hp1 HG03209.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-294+6228G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715480 | |||||||
| chr7:1715524 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0002g0275 a0001c0001t0002g0278 others(2): Show |
5 | NA18943.hp1 NA19009.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-294+6272C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715524 | |||||||
| chr7:1715544 | C | T | 1 | a0001c0001t0009g0122 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-294+6292C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715544 | |||||||
| chr7:1715805 | C | G | 3 | a0001c0001t0001g0244 a0001c0001t0001g0274 a0001c0001t0060g0245 |
3 | HG02135.hp1 NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-294+6553C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715805 | |||||||
| chr7:1715821 | T | C | 17 | a0001c0001t0001g0026 a0001c0001t0001g0290 a0001c0001t0003g0134 others(14): Show |
17 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-294+6569T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715821 | |||||||
| chr7:1715821 | T | G | 1 | a0001c0002t0004g0235 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-294+6569T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715821 | |||||||
| chr7:1715858 | C | T | 2 | a0001c0001t0001g0003 a0001c0018t0001g0003 |
2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-294+6606C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1715858 | |||||||
| chr7:1716103 | A | G | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(289): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-294+6851A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716103 | |||||||
| chr7:1716331 | A | G | 16 | a0001c0001t0001g0026 a0001c0001t0001g0290 a0001c0001t0003g0134 others(13): Show |
16 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-294+7079A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716331 | |||||||
| chr7:1716341 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-294+7089G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716341 | |||||||
| chr7:1716349 | G | A | 1 | a0001c0011t0034g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-294+7097G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716349 | |||||||
| chr7:1716370 | C | T | 1 | a0001c0002t0004g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-294+7118C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716370 | |||||||
| chr7:1716372 | T | G | 2 | a0001c0001t0025g0054 a0001c0001t0035g0055 |
2 | HG02622.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-294+7120T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716372 | |||||||
| chr7:1716648 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0146 a0001c0001t0001g0157 others(46): Show |
51 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.-294+7396G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716648 | |||||||
| chr7:1716850 | G | C | 6 | a0001c0001t0001g0254 a0001c0001t0013g0198 a0001c0002t0004g0235 others(3): Show |
6 | HG00639.hp1 NA18947.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-294+7598G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716850 | |||||||
| chr7:1716862 | G | A | 9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-294+7610G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716862 | |||||||
| chr7:1716908 | A | G | 1 | a0001c0001t0008g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-294+7656A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1716908 | |||||||
| chr7:1717010 | A | G | 1 | a0002c0003t0003g0022 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-294+7758A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717010 | |||||||
| chr7:1717153 | G | A | 7 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0055g0288 others(4): Show |
8 | HG02280.hp2 HG02630.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-294+7901G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717153 | |||||||
| chr7:1717156 | C | T | 1 | a0001c0001t0025g0012 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-294+7904C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717156 | |||||||
| chr7:1717398 | G | A | 14 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(11): Show |
14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+8146G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717398 | |||||||
| chr7:1717490 | G | A | 50 | a0001c0001t0001g0016 a0001c0001t0001g0244 a0001c0001t0001g0251 others(47): Show |
51 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.-294+8238G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717490 | |||||||
| chr7:1717506 | C | T | 11 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+8254C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717506 | |||||||
| chr7:1717600 | T | C | 63 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0146 others(60): Show |
65 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-294+8348T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717600 | |||||||
| chr7:1717615 | G | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0146 others(59): Show |
64 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-294+8363G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717615 | |||||||
| chr7:1717663 | C | T | 1 | a0002c0003t0050g0178 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-294+8411C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717663 | |||||||
| chr7:1717823 | G | A | 1 | a0011c0013t0020g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-294+8571G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717823 | |||||||
| chr7:1717873 | G | T | 2 | a0001c0002t0018g0040 a0001c0002t0018g0041 |
2 | HG00423.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-294+8621G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717873 | |||||||
| chr7:1717969 | A | C | 51 | a0001c0001t0001g0016 a0001c0001t0001g0244 a0001c0001t0001g0251 others(48): Show |
52 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.-294+8717A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1717969 | |||||||
| chr7:1718229 | C | T | 1 | a0006c0010t0045g0150 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-294+8977C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718229 | |||||||
| chr7:1718250 | G | A | 1 | a0001c0001t0015g0175 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-294+8998G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718250 | |||||||
| chr7:1718322 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-294+9070C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718322 | |||||||
| chr7:1718340 | C | A | 1 | a0001c0021t0023g0193 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-294+9088C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718340 | |||||||
| chr7:1718620 | C | T | 1 | a0001c0001t0009g0121 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-294+9368C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718620 | |||||||
| chr7:1718657 | G | A | 1 | a0001c0001t0038g0287 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+9405G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718657 | |||||||
| chr7:1718674 | A | G | 1 | a0002c0003t0003g0022 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-294+9422A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718674 | |||||||
| chr7:1718734 | A | C | 1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-294+9482A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718734 | |||||||
| chr7:1718825 | G | A | 14 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(11): Show |
14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+9573G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718825 | |||||||
| chr7:1718861 | G | A | 1 | a0001c0001t0038g0287 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+9609G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1718861 | |||||||
| chr7:1719036 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(107): Show |
113 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-294+9784T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719036 | |||||||
| chr7:1719083 | C | G | 14 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(11): Show |
14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+9831C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719083 | |||||||
| chr7:1719118 | ACCCCGCC others(119): Show |
A | 1 | a0001c0021t0023g0193 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-294+9974_-294+100 others(5): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719118 | ||||||
| chr7:1719123 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-294+9871G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719123 | |||||||
| chr7:1719142 | GCCACCAA others(11): Show |
G | 1 | a0001c0001t0001g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-294+9920_-294+993 others(22): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719142 | ||||||
| chr7:1719146 | C | G | 1 | a0001c0001t0038g0287 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+9894C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719146 | |||||||
| chr7:1719160 | C | CCCACCAA others(29): Show |
1 | a0001c0002t0004g0280 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-294+10010_-294+10 others(42): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719160 | ||||||
| chr7:1719160 | CCCACCAA others(29): Show |
C | 1 | a0001c0001t0002g0066 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-294+10010_-294+10 others(42): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719160 | ||||||
| chr7:1719163 | A | ACCAACAG others(61): Show |
14 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(11): Show |
14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+9919_-294+992 others(72): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719163 | ||||||
| chr7:1719163 | A | ACCAACAG others(43): Show |
1 | a0001c0001t0038g0287 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+9919_-294+992 others(54): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719163 | ||||||
| chr7:1719163 | A | ACCAACAG others(61): Show |
10 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(7): Show |
11 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+9919_-294+992 others(72): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719163 | ||||||
| chr7:1719226 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+9974A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719226 | |||||||
| chr7:1719230 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+9978A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719230 | |||||||
| chr7:1719231 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+9979A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719231 | |||||||
| chr7:1719232 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+9980G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719232 | |||||||
| chr7:1719232 | GCCACCAA others(47): Show |
G | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-294+10085_-294+10 others(60): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719232 | ||||||
| chr7:1719260 | GGACCCAA others(28): Show |
G | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+10010_-294+10 others(41): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719260 | ||||||
| chr7:1719262 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-294+10010A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719262 | |||||||
| chr7:1719266 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-294+10014A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719266 | |||||||
| chr7:1719267 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-294+10015A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719267 | |||||||
| chr7:1719268 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-294+10016G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719268 | |||||||
| chr7:1719268 | G | GCCACCAA others(11): Show |
102 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0030 others(99): Show |
103 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-294+10046_-294+10 others(24): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719268 | ||||||
| chr7:1719268 | G | GCCACCAA others(83): Show |
1 | a0001c0002t0003g0214 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-294+10045_-294+10 others(96): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719268 | ||||||
| chr7:1719268 | G | GCCACCAA others(29): Show |
2 | a0001c0001t0012g0148 a0001c0001t0065g0286 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-294+10028_-294+10 others(42): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719268 | ||||||
| chr7:1719268 | G | GCCACCAA others(137): Show |
1 | a0001c0001t0001g0023 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-294+10063_-294+10 others(150): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719268 | ||||||
| chr7:1719289 | A | ACCAACAG others(7): Show |
9 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0005g0149 others(6): Show |
10 | HG02280.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-294+10040_-294+10 others(20): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719289 | ||||||
| chr7:1719289 | A | ACCAACAG others(25): Show |
16 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(13): Show |
16 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-294+10063_-294+10 others(38): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719289 | ||||||
| chr7:1719298 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-294+10046G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719298 | |||||||
| chr7:1719298 | G | GCCCCGCC others(12): Show |
1 | a0001c0001t0003g0047 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-294+10063_-294+10 others(25): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719298 | ||||||
| chr7:1719298 | G | GCCCCGCC others(30): Show |
36 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0238 others(33): Show |
38 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.-294+10063_-294+10 others(43): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719298 | ||||||
| chr7:1719315 | G | GGCCCCGC others(11): Show |
1 | a0001c0001t0007g0266 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-294+10063_-294+10 others(24): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719315 | |||||||
| chr7:1719316 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+10064A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719316 | |||||||
| chr7:1719320 | A | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+10068A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719320 | |||||||
| chr7:1719321 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+10069A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719321 | |||||||
| chr7:1719322 | G | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+10070G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719322 | |||||||
| chr7:1719340 | C | CCCACCAA others(11): Show |
3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+10099_-294+10 others(24): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719340 | ||||||
| chr7:1719340 | C | CCCACCAA others(65): Show |
25 | a0001c0001t0001g0026 a0001c0001t0001g0146 a0001c0001t0001g0289 others(22): Show |
26 | HG01243.hp2 HG02258.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.-294+10099_-294+10 others(78): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1719340 | ||||||
| chr7:1719447 | C | G | 1 | a0001c0001t0005g0137 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-294+10195C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719447 | |||||||
| chr7:1719753 | G | A | 97 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0053 others(94): Show |
98 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-294+10501G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719753 | |||||||
| chr7:1719759 | G | A | 1 | a0012c0022t0001g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-294+10507G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719759 | |||||||
| chr7:1719904 | C | T | 1 | a0001c0026t0057g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-294+10652C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719904 | |||||||
| chr7:1719914 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-294+10662T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1719914 | |||||||
| chr7:1720007 | A | G | 1 | a0001c0002t0053g0118 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-294+10755A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720007 | |||||||
| chr7:1720151 | G | C | 1 | a0001c0001t0025g0012 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-294+10899G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720151 | |||||||
| chr7:1720226 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-294+10974C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720226 | |||||||
| chr7:1720255 | C | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(51): Show |
56 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-294+11003C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720255 | |||||||
| chr7:1720334 | T | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0238 others(39): Show |
44 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.-294+11082T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720334 | |||||||
| chr7:1720338 | C | G | 1 | a0001c0001t0001g0027 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-294+11086C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720338 | |||||||
| chr7:1720441 | C | A | 1 | a0001c0001t0005g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-294+11189C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720441 | |||||||
| chr7:1720542 | C | G | 1 | a0001c0001t0042g0165 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-294+11290C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720542 | |||||||
| chr7:1720733 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+11481C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720733 | |||||||
| chr7:1720928 | C | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0026 others(51): Show |
56 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.-294+11676C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720928 | |||||||
| chr7:1720935 | T | G | 2 | a0001c0001t0043g0163 a0001c0001t0044g0217 |
2 | NA18948.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-294+11683T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1720935 | |||||||
| chr7:1721030 | T | C | 4 | a0001c0001t0001g0290 a0001c0001t0003g0291 a0002c0003t0050g0178 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-294+11778T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721030 | |||||||
| chr7:1721193 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+11941C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721193 | |||||||
| chr7:1721516 | C | T | 1 | a0001c0001t0038g0287 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+12264C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721516 | |||||||
| chr7:1721570 | G | A | 1 | a0001c0001t0012g0183 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-294+12318G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721570 | |||||||
| chr7:1721623 | G | A | 11 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+12371G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721623 | |||||||
| chr7:1721745 | C | T | 14 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(11): Show |
14 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+12493C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1721745 | |||||||
| chr7:1722265 | C | CT | 7 | a0001c0001t0001g0043 a0001c0001t0001g0233 a0001c0001t0015g0162 others(4): Show |
7 | HG01175.hp2 HG02074.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.-294+13032dupT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1722265 | ||||||
| chr7:1722265 | CT | C | 11 | a0001c0001t0001g0157 a0001c0001t0001g0179 a0001c0001t0002g0226 others(8): Show |
11 | HG01168.hp1 HG01891.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+13032delT | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1722265 | ||||||
| chr7:1722290 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+13038G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722290 | |||||||
| chr7:1722303 | G | C | 1 | a0001c0001t0001g0010 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-294+13051G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722303 | |||||||
| chr7:1722423 | C | T | 1 | a0001c0001t0005g0161 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-294+13171C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722423 | |||||||
| chr7:1722492 | C | G | 1 | a0001c0001t0012g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-294+13240C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722492 | |||||||
| chr7:1722560 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+13308C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722560 | |||||||
| chr7:1722611 | A | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0238 others(38): Show |
43 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.-294+13359A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722611 | |||||||
| chr7:1722864 | G | C | 2 | a0001c0001t0001g0087 a0001c0001t0021g0082 |
2 | HG00735.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.-294+13612G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1722864 | |||||||
| chr7:1723060 | G | A | 1 | a0001c0001t0006g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-294+13808G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723060 | |||||||
| chr7:1723087 | G | A | 2 | a0001c0001t0001g0003 a0001c0018t0001g0003 |
2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-294+13835G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723087 | |||||||
| chr7:1723202 | A | T | 3 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0003c0006t0016g0181 |
3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+13950A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723202 | |||||||
| chr7:1723298 | G | A | 3 | a0001c0001t0001g0053 a0001c0001t0025g0054 a0001c0001t0035g0055 |
3 | HG02622.hp1 HG02809.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-294+14046G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723298 | |||||||
| chr7:1723311 | A | G | 1 | a0015c0023t0003g0131 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-294+14059A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723311 | |||||||
| chr7:1723358 | C | T | 1 | a0001c0001t0051g0019 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-294+14106C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723358 | |||||||
| chr7:1723486 | C | G | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-294+14234C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723486 | |||||||
| chr7:1723528 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0203 a0001c0001t0001g0213 others(46): Show |
50 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-294+14276G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723528 | |||||||
| chr7:1723548 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0088 |
2 | HG01261.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.-294+14296T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723548 | |||||||
| chr7:1723591 | C | T | 1 | a0015c0023t0003g0131 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-294+14339C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723591 | |||||||
| chr7:1723657 | G | T | 1 | a0001c0027t0062g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-294+14405G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723657 | |||||||
| chr7:1723683 | C | T | 1 | a0001c0002t0004g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-294+14431C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723683 | |||||||
| chr7:1723809 | A | G | 14 | a0001c0001t0001g0146 a0001c0001t0001g0289 a0001c0001t0006g0036 others(11): Show |
15 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-294+14557A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723809 | |||||||
| chr7:1723810 | C | T | 3 | a0001c0001t0012g0148 a0001c0001t0065g0286 a0003c0006t0016g0181 |
3 | HG02145.hp2 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-294+14558C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723810 | |||||||
| chr7:1723819 | G | A | 1 | a0001c0001t0001g0234 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-294+14567G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723819 | |||||||
| chr7:1723877 | A | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0177 a0001c0018t0001g0003 |
3 | HG00733.hp2 HG01081.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-294+14625A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723877 | |||||||
| chr7:1723911 | G | A | 1 | a0001c0001t0038g0287 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-294+14659G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1723911 | |||||||
| chr7:1724087 | G | A | 14 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(11): Show |
14 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+14835G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724087 | |||||||
| chr7:1724099 | C | G | 74 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(71): Show |
76 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.-294+14847C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724099 | |||||||
| chr7:1724103 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-294+14851C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724103 | |||||||
| chr7:1724187 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-294+14935C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724187 | |||||||
| chr7:1724393 | T | C | 3 | a0001c0001t0001g0069 a0001c0001t0002g0071 a0001c0001t0063g0072 |
3 | HG01106.hp1 HG01168.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-294+15141T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724393 | |||||||
| chr7:1724550 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-294+15298A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724550 | |||||||
| chr7:1724674 | A | G | 1 | a0001c0001t0008g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-294+15422A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724674 | |||||||
| chr7:1724704 | G | C | 1 | a0014c0020t0002g0062 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-294+15452G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724704 | |||||||
| chr7:1724709 | T | TC | 11 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(8): Show |
11 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-294+15463dupC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1724709 | ||||||
| chr7:1724714 | C | G | 10 | a0001c0001t0002g0208 a0001c0001t0004g0204 a0001c0001t0004g0205 others(7): Show |
10 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.-294+15462C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724714 | |||||||
| chr7:1724806 | A | G | 1 | a0001c0001t0012g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-294+15554A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724806 | |||||||
| chr7:1724807 | A | G | 65 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0027 others(62): Show |
66 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-294+15555A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724807 | |||||||
| chr7:1724836 | G | C | 47 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0002g0116 others(44): Show |
48 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-294+15584G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724836 | |||||||
| chr7:1724863 | C | T | 1 | a0001c0001t0012g0021 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-294+15611C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724863 | |||||||
| chr7:1724915 | T | TA | 14 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(11): Show |
14 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-294+15664dupA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1724915 | ||||||
| chr7:1724949 | G | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0023 others(174): Show |
180 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.-294+15697G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724949 | |||||||
| chr7:1724957 | A | C | 3 | a0001c0001t0025g0012 a0001c0001t0038g0287 a0002c0024t0030g0028 |
3 | HG02818.hp2 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-294+15705A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724957 | |||||||
| chr7:1724977 | G | A | 1 | a0001c0001t0026g0136 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-294+15725G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1724977 | |||||||
| chr7:1725279 | G | A | 1 | a0001c0011t0034g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-294+16027G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725279 | |||||||
| chr7:1725523 | G | A | 1 | a0001c0001t0056g0194 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-294+16271G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725523 | |||||||
| chr7:1725547 | A | AGTCACTC others(8): Show |
1 | a0001c0001t0011g0106 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-294+16298_-294+16 others(21): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1725547 | ||||||
| chr7:1725648 | C | T | 1 | a0001c0001t0016g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-294+16396C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725648 | |||||||
| chr7:1725705 | G | A | 11 | a0001c0001t0001g0244 a0001c0001t0001g0251 a0001c0001t0001g0274 others(8): Show |
12 | HG02083.hp1 HG02135.hp1 NA18946.hp2 others(9): Show |
intron_variant | MODIFIER | c.-294+16453G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725705 | |||||||
| chr7:1725849 | CA | C | 9 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(6): Show |
9 | HG02145.hp2 HG02258.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.-294+16601delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1725849 | ||||||
| chr7:1725929 | C | T | 1 | a0001c0011t0034g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-294+16677C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725929 | |||||||
| chr7:1725940 | A | C | 1 | a0001c0001t0011g0106 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-294+16688A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725940 | |||||||
| chr7:1725947 | C | T | 2 | a0001c0001t0009g0051 a0001c0001t0009g0052 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-294+16695C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725947 | |||||||
| chr7:1725956 | G | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0023 others(166): Show |
172 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.-294+16704G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1725956 | |||||||
| chr7:1725959 | A | ACACT | 98 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0027 others(95): Show |
100 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-294+16710_-294+16 others(10): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1725959 | ||||||
| chr7:1726024 | A | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0143 a0001c0001t0012g0021 others(1): Show |
4 | HG00639.hp2 HG01496.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-294+16772A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726024 | |||||||
| chr7:1726124 | T | C | 2 | a0001c0001t0005g0161 a0001c0001t0055g0288 |
2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-294+16872T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726124 | |||||||
| chr7:1726256 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-294+17004T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726256 | |||||||
| chr7:1726446 | A | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0187 others(56): Show |
61 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-294+17194A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726446 | |||||||
| chr7:1726459 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-294+17207G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726459 | |||||||
| chr7:1726659 | T | C | 18 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(15): Show |
19 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.-294+17407T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726659 | |||||||
| chr7:1726676 | C | G | 12 | a0001c0001t0001g0053 a0001c0001t0001g0289 a0001c0001t0008g0018 others(9): Show |
12 | HG00639.hp2 HG01255.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-294+17424C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726676 | |||||||
| chr7:1726715 | A | T | 2 | a0001c0001t0001g0290 a0001c0001t0005g0056 |
2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-294+17463A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726715 | |||||||
| chr7:1726927 | C | T | 12 | a0001c0001t0001g0053 a0001c0001t0001g0289 a0001c0001t0008g0018 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-293-17377C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726927 | |||||||
| chr7:1726986 | C | G | 6 | a0001c0001t0008g0124 a0001c0001t0008g0132 a0001c0001t0020g0017 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-17318C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1726986 | |||||||
| chr7:1727034 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0244 others(50): Show |
55 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-293-17270C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727034 | |||||||
| chr7:1727113 | G | A | 3 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0013c0012t0032g0158 |
3 | HG02717.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-293-17191G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727113 | |||||||
| chr7:1727264 | C | T | 1 | a0001c0001t0003g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-293-17040C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727264 | |||||||
| chr7:1727389 | C | G | 1 | a0001c0002t0004g0096 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-293-16915C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727389 | |||||||
| chr7:1727437 | G | A | 6 | a0001c0001t0001g0146 a0001c0001t0005g0149 a0001c0001t0025g0012 others(3): Show |
7 | HG02630.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.-293-16867G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727437 | |||||||
| chr7:1727477 | GTGCCCCT others(16): Show |
G | 19 | a0001c0001t0001g0053 a0001c0001t0001g0289 a0001c0001t0008g0018 others(16): Show |
19 | HG01243.hp2 HG01255.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-293-16821_-293-16 others(29): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1727477 | ||||||
| chr7:1727518 | C | A | 1 | a0001c0002t0001g0242 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-293-16786C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727518 | |||||||
| chr7:1727547 | G | T | 4 | a0001c0001t0001g0187 a0001c0001t0003g0032 a0001c0001t0006g0036 others(1): Show |
4 | HG01884.hp2 HG02895.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-16757G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727547 | |||||||
| chr7:1727611 | G | A | 11 | a0001c0001t0001g0053 a0001c0001t0001g0289 a0001c0001t0008g0018 others(8): Show |
11 | HG01255.hp1 HG02280.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-293-16693G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727611 | |||||||
| chr7:1727792 | T | G | 7 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0001c0025t0058g0046 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-16512T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727792 | |||||||
| chr7:1727826 | T | C | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-293-16478T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727826 | |||||||
| chr7:1727972 | C | T | 1 | a0001c0001t0015g0169 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-293-16332C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727972 | |||||||
| chr7:1727989 | C | T | 15 | a0001c0001t0001g0126 a0001c0001t0003g0024 a0001c0001t0005g0285 others(12): Show |
15 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-293-16315C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727989 | |||||||
| chr7:1727994 | T | C | 1 | a0001c0001t0008g0029 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-293-16310T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1727994 | |||||||
| chr7:1728070 | C | T | 4 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0001c0025t0058g0046 others(1): Show |
4 | HG01109.hp2 HG02976.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-16234C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728070 | |||||||
| chr7:1728169 | C | CAG | 293 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(290): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-293-16135_-293-16 others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728169 | |||||||
| chr7:1728285 | C | T | 6 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(3): Show |
6 | HG02622.hp2 HG02895.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-16019C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728285 | |||||||
| chr7:1728286 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-293-16018G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728286 | |||||||
| chr7:1728419 | C | T | 7 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(4): Show |
7 | HG02622.hp2 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-15885C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728419 | |||||||
| chr7:1728444 | C | T | 6 | a0001c0001t0008g0124 a0001c0001t0008g0132 a0001c0001t0020g0017 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-15860C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728444 | |||||||
| chr7:1728474 | C | G | 13 | a0001c0001t0001g0053 a0001c0001t0001g0289 a0001c0001t0008g0018 others(10): Show |
13 | HG01255.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-293-15830C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728474 | |||||||
| chr7:1728859 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(4): Show |
7 | HG02622.hp2 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-15445G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1728859 | |||||||
| chr7:1728903 | T | TCATCATC others(10): Show |
2 | a0001c0001t0001g0203 a0001c0001t0001g0215 |
2 | NA18960.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-293-15385_-293-15 others(23): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1728903 | ||||||
| chr7:1729023 | C | T | 1 | a0001c0001t0015g0162 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-293-15281C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729023 | |||||||
| chr7:1729024 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-293-15280G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729024 | |||||||
| chr7:1729025 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-293-15279G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729025 | |||||||
| chr7:1729129 | C | T | 1 | a0001c0004t0061g0269 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-293-15175C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729129 | |||||||
| chr7:1729153 | A | G | 5 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0001c0027t0062g0199 others(2): Show |
5 | HG01109.hp2 HG02280.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-293-15151A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729153 | |||||||
| chr7:1729267 | T | G | 1 | a0001c0001t0006g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-293-15037T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729267 | |||||||
| chr7:1729403 | G | A | 19 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(16): Show |
20 | HG01109.hp2 HG02109.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-293-14901G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729403 | |||||||
| chr7:1729532 | G | A | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-293-14772G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729532 | |||||||
| chr7:1729716 | C | T | 2 | a0001c0001t0005g0137 a0001c0001t0005g0155 |
2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-293-14588C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729716 | |||||||
| chr7:1729750 | T | C | 11 | a0001c0001t0003g0047 a0001c0001t0006g0119 a0001c0001t0006g0282 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-293-14554T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729750 | |||||||
| chr7:1729837 | A | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0244 others(51): Show |
56 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.-293-14467A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729837 | |||||||
| chr7:1729914 | G | A | 4 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0001c0025t0058g0046 others(1): Show |
4 | HG01109.hp2 HG02976.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-14390G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729914 | |||||||
| chr7:1729948 | C | T | 1 | a0001c0001t0006g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-293-14356C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729948 | |||||||
| chr7:1729996 | C | G | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-293-14308C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1729996 | |||||||
| chr7:1730054 | G | A | 3 | a0001c0001t0001g0289 a0001c0001t0055g0288 a0001c0001t0064g0014 |
3 | HG01255.hp1 HG02280.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-293-14250G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730054 | |||||||
| chr7:1730067 | C | T | 1 | a0001c0001t0005g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-293-14237C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730067 | |||||||
| chr7:1730083 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-293-14221G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730083 | |||||||
| chr7:1730182 | G | A | 1 | a0001c0001t0047g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-293-14122G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730182 | |||||||
| chr7:1730390 | C | T | 1 | a0001c0001t0006g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-293-13914C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730390 | |||||||
| chr7:1730464 | A | G | 10 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(7): Show |
10 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-293-13840A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730464 | |||||||
| chr7:1730533 | T | G | 2 | a0001c0001t0002g0197 a0001c0001t0002g0222 |
2 | HG02155.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-293-13771T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730533 | |||||||
| chr7:1730631 | C | T | 1 | a0001c0001t0004g0205 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-293-13673C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730631 | |||||||
| chr7:1730905 | A | G | 36 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(33): Show |
37 | HG00639.hp2 HG01243.hp2 HG01255.hp1 others(34): Show |
intron_variant | MODIFIER | c.-293-13399A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1730905 | |||||||
| chr7:1731164 | T | C | 6 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(3): Show |
6 | HG02622.hp2 HG02895.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-13140T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731164 | |||||||
| chr7:1731312 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0244 others(51): Show |
56 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.-293-12992A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731312 | |||||||
| chr7:1731618 | G | A | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-293-12686G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731618 | |||||||
| chr7:1731630 | G | A | 1 | a0013c0012t0032g0158 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-293-12674G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731630 | |||||||
| chr7:1731636 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0244 others(50): Show |
55 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-293-12668G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731636 | |||||||
| chr7:1731727 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-293-12577C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731727 | |||||||
| chr7:1731737 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-293-12567C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731737 | |||||||
| chr7:1731753 | G | A | 5 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0001g0290 others(2): Show |
5 | HG02559.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-293-12551G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731753 | |||||||
| chr7:1731839 | G | A | 19 | a0001c0001t0007g0164 a0001c0001t0007g0166 a0001c0001t0007g0167 others(16): Show |
19 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.-293-12465G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731839 | |||||||
| chr7:1731892 | T | C | 293 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(290): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-293-12412T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1731892 | |||||||
| chr7:1732062 | C | T | 3 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0002c0003t0050g0178 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-12242C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732062 | |||||||
| chr7:1732124 | G | A | 1 | a0001c0025t0058g0046 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-293-12180G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732124 | |||||||
| chr7:1732171 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-293-12133A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732171 | |||||||
| chr7:1732172 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-293-12132G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732172 | |||||||
| chr7:1732231 | G | A | 3 | a0001c0001t0005g0137 a0001c0001t0005g0155 a0002c0003t0006g0013 |
3 | HG01243.hp1 HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-293-12073G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732231 | |||||||
| chr7:1732440 | C | T | 3 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0002c0003t0050g0178 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-11864C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732440 | |||||||
| chr7:1732466 | A | T | 1 | a0001c0001t0005g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-293-11838A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732466 | |||||||
| chr7:1732559 | T | C | 20 | a0001c0001t0001g0053 a0001c0001t0001g0187 a0001c0001t0001g0289 others(17): Show |
20 | HG01243.hp2 HG01255.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.-293-11745T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732559 | |||||||
| chr7:1732993 | T | C | 6 | a0001c0001t0008g0124 a0001c0001t0008g0132 a0001c0001t0020g0017 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-11311T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1732993 | |||||||
| chr7:1733003 | C | A | 2 | a0001c0001t0001g0290 a0001c0001t0005g0056 |
2 | HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-293-11301C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733003 | |||||||
| chr7:1733061 | C | T | 2 | a0001c0001t0020g0017 a0001c0001t0020g0133 |
2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-293-11243C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733061 | |||||||
| chr7:1733104 | T | C | 7 | a0001c0001t0006g0119 a0001c0001t0006g0282 a0001c0001t0012g0183 others(4): Show |
7 | HG01167.hp2 HG02145.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-11200T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733104 | |||||||
| chr7:1733143 | C | T | 1 | a0001c0002t0004g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-293-11161C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733143 | |||||||
| chr7:1733285 | G | A | 8 | a0001c0001t0006g0119 a0001c0001t0006g0282 a0001c0001t0012g0183 others(5): Show |
8 | HG01167.hp2 HG02145.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-293-11019G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733285 | |||||||
| chr7:1733320 | G | A | 2 | a0004c0008t0028g0284 a0004c0008t0029g0283 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-293-10984G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733320 | |||||||
| chr7:1733442 | G | A | 14 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(11): Show |
14 | HG01167.hp2 HG02145.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.-293-10862G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733442 | |||||||
| chr7:1733566 | C | G | 1 | a0006c0010t0046g0151 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-293-10738C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733566 | |||||||
| chr7:1733566 | C | T | 3 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0002c0003t0050g0178 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-10738C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733566 | |||||||
| chr7:1733626 | C | T | 7 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(4): Show |
7 | HG02622.hp2 HG02895.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-10678C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733626 | |||||||
| chr7:1733744 | T | C | 4 | a0001c0001t0009g0051 a0001c0001t0009g0052 a0001c0001t0009g0120 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-10560T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1733744 | |||||||
| chr7:1734044 | C | A | 1 | a0001c0001t0025g0054 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-293-10260C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734044 | |||||||
| chr7:1734092 | C | G | 14 | a0001c0001t0001g0053 a0001c0001t0001g0187 a0001c0001t0001g0289 others(11): Show |
14 | HG01255.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-293-10212C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734092 | |||||||
| chr7:1734139 | G | T | 2 | a0001c0025t0058g0046 a0002c0024t0030g0028 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-293-10165G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734139 | |||||||
| chr7:1734267 | C | T | 5 | a0001c0001t0001g0023 a0001c0001t0001g0143 a0002c0003t0024g0045 others(2): Show |
5 | HG02055.hp1 HG02647.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-293-10037C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734267 | |||||||
| chr7:1734314 | G | A | 1 | a0002c0003t0024g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-293-9990G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734314 | |||||||
| chr7:1734360 | C | T | 56 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(53): Show |
57 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.-293-9944C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734360 | |||||||
| chr7:1734729 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-293-9575T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734729 | |||||||
| chr7:1734784 | A | G | 1 | a0001c0001t0004g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-293-9520A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734784 | |||||||
| chr7:1734842 | C | T | 3 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0002c0003t0050g0178 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-9462C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734842 | |||||||
| chr7:1734952 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-293-9352C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1734952 | |||||||
| chr7:1735054 | G | A | 2 | a0002c0003t0024g0145 a0002c0003t0024g0182 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-293-9250G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735054 | |||||||
| chr7:1735109 | C | G | 2 | a0001c0025t0058g0046 a0002c0024t0030g0028 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-293-9195C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735109 | |||||||
| chr7:1735135 | C | T | 1 | a0001c0001t0011g0212 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-293-9169C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735135 | |||||||
| chr7:1735167 | T | A | 28 | a0001c0001t0001g0098 a0001c0001t0001g0213 a0001c0001t0002g0113 others(25): Show |
28 | HG00558.hp1 HG00639.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-293-9137T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735167 | |||||||
| chr7:1735170 | A | G | 61 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(58): Show |
62 | HG00558.hp1 HG00639.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.-293-9134A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735170 | |||||||
| chr7:1735175 | G | T | 6 | a0001c0001t0008g0124 a0001c0001t0008g0132 a0001c0001t0020g0017 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-9129G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735175 | |||||||
| chr7:1735191 | G | A | 4 | a0001c0001t0005g0219 a0001c0001t0005g0231 a0001c0001t0005g0232 others(1): Show |
4 | HG02083.hp2 NA18946.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-9113G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735191 | |||||||
| chr7:1735199 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-293-9105G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735199 | |||||||
| chr7:1735201 | C | T | 1 | a0001c0001t0065g0286 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-293-9103C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735201 | |||||||
| chr7:1735229 | A | T | 1 | a0011c0013t0020g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-293-9075A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735229 | |||||||
| chr7:1735269 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-293-9035G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735269 | |||||||
| chr7:1735276 | T | C | 2 | a0001c0001t0026g0020 a0001c0001t0051g0019 |
2 | HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-293-9028T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735276 | |||||||
| chr7:1735312 | A | C | 25 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(22): Show |
26 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.-293-8992A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735312 | |||||||
| chr7:1735460 | G | C | 39 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(36): Show |
40 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.-293-8844G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735460 | |||||||
| chr7:1735529 | C | T | 1 | a0001c0001t0031g0102 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-293-8775C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735529 | |||||||
| chr7:1735607 | A | G | 45 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0030 others(42): Show |
46 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.-293-8697A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735607 | |||||||
| chr7:1735958 | G | A | 1 | a0001c0001t0023g0195 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-293-8346G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1735958 | |||||||
| chr7:1736086 | C | G | 1 | a0002c0024t0030g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-293-8218C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736086 | |||||||
| chr7:1736092 | C | G | 6 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0001g0290 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-8212C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736092 | |||||||
| chr7:1736272 | T | TC | 6 | a0001c0001t0008g0124 a0001c0001t0008g0132 a0001c0001t0020g0017 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-8027dupC | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1736272 | ||||||
| chr7:1736282 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-293-8022G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736282 | |||||||
| chr7:1736325 | G | A | 17 | a0001c0001t0007g0164 a0001c0001t0007g0166 a0001c0001t0007g0167 others(14): Show |
17 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-7979G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736325 | |||||||
| chr7:1736441 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0143 a0003c0006t0016g0181 others(1): Show |
4 | HG02055.hp1 HG02647.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-7863G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736441 | |||||||
| chr7:1736539 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-293-7765C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736539 | |||||||
| chr7:1736572 | C | G | 1 | a0002c0003t0050g0178 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-293-7732C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736572 | |||||||
| chr7:1736730 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-293-7574T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736730 | |||||||
| chr7:1736796 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0244 others(50): Show |
55 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.-293-7508G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736796 | |||||||
| chr7:1736851 | C | T | 1 | a0001c0001t0022g0076 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-293-7453C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736851 | |||||||
| chr7:1736862 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-7442C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736862 | |||||||
| chr7:1736945 | GA | G | 17 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(14): Show |
17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-7358delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736945 | |||||||
| chr7:1736947 | T | C | 17 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(14): Show |
17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-7357T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736947 | |||||||
| chr7:1736985 | C | G | 1 | a0001c0001t0031g0102 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-293-7319C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1736985 | |||||||
| chr7:1737080 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-293-7224G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737080 | |||||||
| chr7:1737108 | C | A | 5 | a0001c0001t0002g0066 a0001c0001t0002g0077 a0001c0001t0002g0171 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.-293-7196C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737108 | |||||||
| chr7:1737127 | C | G | 1 | a0001c0001t0011g0106 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-293-7177C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737127 | |||||||
| chr7:1737330 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-293-6974T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737330 | |||||||
| chr7:1737331 | C | A | 1 | a0001c0001t0001g0016 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-293-6973C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737331 | |||||||
| chr7:1737332 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-293-6972A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737332 | |||||||
| chr7:1737378 | G | A | 3 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0002c0003t0050g0178 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-6926G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737378 | |||||||
| chr7:1737709 | G | A | 6 | a0001c0001t0008g0124 a0001c0001t0008g0132 a0001c0001t0020g0017 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-6595G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737709 | |||||||
| chr7:1737777 | T | C | 24 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0043 others(21): Show |
25 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-293-6527T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737777 | |||||||
| chr7:1737821 | C | T | 4 | a0001c0001t0005g0219 a0001c0001t0005g0231 a0001c0001t0005g0232 others(1): Show |
4 | HG02083.hp2 NA18946.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-6483C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737821 | |||||||
| chr7:1737980 | C | G | 1 | a0001c0001t0019g0153 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-293-6324C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1737980 | |||||||
| chr7:1738001 | C | T | 2 | a0001c0025t0058g0046 a0002c0024t0030g0028 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-293-6303C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738001 | |||||||
| chr7:1738030 | G | A | 1 | a0011c0013t0020g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-293-6274G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738030 | |||||||
| chr7:1738050 | C | T | 17 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(14): Show |
17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-6254C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738050 | |||||||
| chr7:1738188 | A | T | 1 | a0001c0001t0005g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-293-6116A>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738188 | |||||||
| chr7:1738330 | C | T | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-293-5974C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738330 | |||||||
| chr7:1738392 | A | G | 1 | a0015c0023t0003g0131 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-293-5912A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738392 | |||||||
| chr7:1738406 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0140 |
2 | HG00621.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-293-5898C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738406 | |||||||
| chr7:1738590 | G | T | 17 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(14): Show |
17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-5714G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738590 | |||||||
| chr7:1738710 | C | T | 3 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0030g0007 |
4 | NA18964.hp2 NA18995.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-5594C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738710 | |||||||
| chr7:1738720 | G | A | 5 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0001g0290 others(2): Show |
5 | HG02559.hp2 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-293-5584G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738720 | |||||||
| chr7:1738731 | C | T | 1 | a0001c0001t0025g0012 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-293-5573C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738731 | |||||||
| chr7:1738746 | C | T | 17 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(14): Show |
17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-5558C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738746 | |||||||
| chr7:1738934 | C | G | 1 | a0002c0003t0050g0178 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-293-5370C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738934 | |||||||
| chr7:1738968 | C | T | 12 | a0001c0001t0005g0285 a0001c0001t0006g0129 a0001c0001t0009g0051 others(9): Show |
12 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-293-5336C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1738968 | |||||||
| chr7:1739007 | C | T | 3 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0002c0003t0050g0178 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-5297C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739007 | |||||||
| chr7:1739071 | C | T | 7 | a0001c0001t0007g0201 a0001c0001t0008g0124 a0001c0001t0008g0132 others(4): Show |
7 | HG00621.hp1 HG01243.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-293-5233C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739071 | |||||||
| chr7:1739105 | C | T | 133 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0023 others(130): Show |
136 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-293-5199C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739105 | |||||||
| chr7:1739114 | G | A | 2 | a0001c0025t0058g0046 a0002c0024t0030g0028 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-293-5190G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739114 | |||||||
| chr7:1739127 | C | A | 2 | a0001c0001t0011g0086 a0001c0001t0011g0240 |
2 | NA18612.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-293-5177C>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739127 | |||||||
| chr7:1739139 | T | A | 1 | a0001c0001t0005g0219 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-293-5165T>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739139 | |||||||
| chr7:1739166 | G | T | 1 | a0001c0001t0047g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-293-5138G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739166 | |||||||
| chr7:1739221 | T | C | 2 | a0001c0001t0012g0210 a0001c0001t0012g0211 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-293-5083T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739221 | |||||||
| chr7:1739248 | C | T | 6 | a0001c0001t0008g0124 a0001c0001t0008g0132 a0001c0001t0020g0017 others(3): Show |
6 | HG01243.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-5056C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739248 | |||||||
| chr7:1739265 | G | A | 1 | a0002c0003t0003g0022 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-293-5039G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739265 | |||||||
| chr7:1739317 | T | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0026 others(91): Show |
96 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-293-4987T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739317 | |||||||
| chr7:1739351 | C | G | 1 | a0002c0003t0024g0045 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-293-4953C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739351 | |||||||
| chr7:1739448 | C | T | 4 | a0001c0001t0001g0289 a0001c0001t0029g0031 a0001c0001t0055g0288 others(1): Show |
4 | HG01255.hp1 HG02280.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-4856C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739448 | |||||||
| chr7:1739473 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0023 others(98): Show |
103 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.-293-4831C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739473 | |||||||
| chr7:1739611 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-293-4693G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739611 | |||||||
| chr7:1739733 | C | T | 2 | a0001c0001t0011g0086 a0001c0001t0011g0240 |
2 | NA18612.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-293-4571C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739733 | |||||||
| chr7:1739757 | G | C | 1 | a0001c0002t0004g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-293-4547G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739757 | |||||||
| chr7:1739828 | G | A | 3 | a0001c0001t0012g0183 a0002c0003t0024g0145 a0002c0003t0024g0182 |
3 | HG01167.hp2 HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-293-4476G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1739828 | |||||||
| chr7:1740003 | C | T | 3 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0002c0003t0050g0178 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-4301C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740003 | |||||||
| chr7:1740161 | G | A | 1 | a0001c0001t0002g0113 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-293-4143G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740161 | |||||||
| chr7:1740303 | G | A | 2 | a0001c0025t0058g0046 a0002c0024t0030g0028 |
2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-293-4001G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740303 | |||||||
| chr7:1740430 | C | T | 1 | a0001c0001t0003g0032 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-293-3874C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740430 | |||||||
| chr7:1740702 | C | T | 17 | a0001c0001t0001g0026 a0001c0001t0003g0134 a0001c0001t0003g0135 others(14): Show |
17 | HG01167.hp2 HG01243.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-293-3602C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740702 | |||||||
| chr7:1740804 | C | T | 1 | a0009c0015t0032g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-293-3500C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740804 | |||||||
| chr7:1740807 | G | A | 2 | a0001c0001t0003g0291 a0001c0001t0019g0064 |
2 | HG02559.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-293-3497G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740807 | |||||||
| chr7:1740928 | G | A | 1 | a0001c0002t0018g0228 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-293-3376G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1740928 | |||||||
| chr7:1741062 | A | G | 1 | a0001c0001t0002g0197 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-293-3242A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741062 | |||||||
| chr7:1741111 | C | G | 1 | a0001c0001t0003g0032 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-293-3193C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741111 | |||||||
| chr7:1741129 | C | CA | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(194): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.-293-3156dupA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1741129 | ||||||
| chr7:1741129 | C | CAA | 17 | a0001c0001t0001g0079 a0001c0001t0001g0094 a0001c0001t0001g0213 others(14): Show |
17 | HG01167.hp1 HG01169.hp1 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.-293-3157_-293-315 others(6): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1741129 | ||||||
| chr7:1741129 | CA | C | 22 | a0001c0001t0001g0053 a0001c0001t0001g0289 a0001c0001t0002g0071 others(19): Show |
22 | HG00639.hp2 HG01168.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.-293-3156delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1741129 | ||||||
| chr7:1741231 | C | G | 3 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0002c0003t0050g0178 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-3073C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741231 | |||||||
| chr7:1741252 | C | T | 1 | a0001c0002t0004g0260 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-293-3052C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741252 | |||||||
| chr7:1741263 | C | T | 3 | a0001c0001t0003g0047 a0001c0001t0038g0287 a0002c0003t0050g0178 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-3041C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741263 | |||||||
| chr7:1741308 | G | C | 1 | a0001c0011t0034g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-293-2996G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741308 | |||||||
| chr7:1741318 | C | T | 1 | a0001c0001t0006g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-293-2986C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741318 | |||||||
| chr7:1741340 | G | T | 13 | a0001c0001t0001g0053 a0001c0001t0003g0032 a0001c0001t0005g0161 others(10): Show |
13 | HG01255.hp1 HG02280.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.-293-2964G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741340 | |||||||
| chr7:1741410 | A | G | 1 | a0002c0024t0030g0028 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-293-2894A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741410 | |||||||
| chr7:1741463 | C | T | 1 | a0001c0001t0005g0221 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-293-2841C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741463 | |||||||
| chr7:1741558 | T | C | 33 | a0001c0001t0001g0053 a0001c0001t0001g0213 a0001c0001t0002g0090 others(30): Show |
33 | HG00639.hp2 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.-293-2746T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741558 | |||||||
| chr7:1741663 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(127): Show |
133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.-293-2641G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741663 | |||||||
| chr7:1741767 | G | C | 1 | a0001c0001t0002g0060 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-293-2537G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741767 | |||||||
| chr7:1741786 | T | C | 293 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(290): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-293-2518T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741786 | |||||||
| chr7:1741805 | C | G | 3 | a0001c0001t0005g0137 a0001c0001t0020g0017 a0001c0001t0020g0133 |
3 | HG02258.hp2 HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-293-2499C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741805 | |||||||
| chr7:1741855 | AGACAGGG others(1275): Show |
A | 1 | a0001c0001t0049g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-293-2445_-293-116 others(4): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1741855 | ||||||
| chr7:1741913 | G | A | 1 | a0001c0001t0052g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-293-2391G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741913 | |||||||
| chr7:1741917 | T | C | 5 | a0001c0001t0001g0159 a0001c0001t0005g0056 a0001c0001t0008g0029 others(2): Show |
5 | HG01496.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-293-2387T>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1741917 | |||||||
| chr7:1741975 | CACAG | C | 16 | a0001c0001t0001g0065 a0001c0001t0001g0088 a0001c0001t0005g0219 others(13): Show |
16 | HG01099.hp1 HG01261.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.-293-2325_-293-232 others(8): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1741975 | ||||||
| chr7:1742000 | G | A | 1 | a0001c0001t0052g0034 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-293-2304G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742000 | |||||||
| chr7:1742025 | T | G | 1 | a0001c0001t0028g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-293-2279T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742025 | |||||||
| chr7:1742151 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0146 |
2 | HG02055.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-293-2153C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742151 | |||||||
| chr7:1742176 | G | A | 3 | a0001c0001t0001g0191 a0002c0003t0050g0178 a0009c0015t0032g0190 |
3 | HG01496.hp1 HG02109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-293-2128G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742176 | |||||||
| chr7:1742297 | C | T | 1 | a0001c0001t0028g0081 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-293-2007C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742297 | |||||||
| chr7:1742376 | G | A | 1 | a0001c0027t0062g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-293-1928G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742376 | |||||||
| chr7:1742396 | C | G | 43 | a0001c0001t0001g0262 a0001c0001t0001g0289 a0001c0001t0002g0060 others(40): Show |
43 | HG00558.hp1 HG00642.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.-293-1908C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742396 | |||||||
| chr7:1742454 | G | A | 1 | a0001c0001t0009g0120 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-293-1850G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742454 | |||||||
| chr7:1742542 | C | T | 3 | a0001c0002t0003g0006 a0001c0002t0003g0007 a0001c0002t0030g0007 |
4 | NA18964.hp2 NA18995.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-1762C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742542 | |||||||
| chr7:1742578 | G | A | 1 | a0001c0001t0005g0218 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-293-1726G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742578 | |||||||
| chr7:1742656 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0143 a0001c0001t0001g0146 others(3): Show |
6 | HG02055.hp1 HG02717.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-293-1648C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742656 | |||||||
| chr7:1742711 | G | A | 1 | a0001c0001t0012g0183 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-293-1593G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742711 | |||||||
| chr7:1742796 | C | T | 6 | a0001c0001t0031g0102 a0001c0001t0040g0048 a0001c0001t0041g0170 others(3): Show |
7 | HG02735.hp1 HG04204.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.-293-1508C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742796 | |||||||
| chr7:1742888 | G | T | 1 | a0001c0002t0004g0280 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-293-1416G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742888 | |||||||
| chr7:1742967 | G | A | 1 | a0004c0008t0029g0283 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-293-1337G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742967 | |||||||
| chr7:1742970 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-293-1334G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1742970 | |||||||
| chr7:1743088 | TG | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(151): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-293-1209delG | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1743088 | ||||||
| chr7:1743137 | G | A | 137 | a0001c0001t0001g0117 a0001c0001t0001g0187 a0001c0001t0001g0262 others(134): Show |
138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-293-1167G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743137 | |||||||
| chr7:1743140 | C | T | 1 | a0001c0002t0004g0270 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-293-1164C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743140 | |||||||
| chr7:1743145 | C | T | 3 | a0001c0001t0003g0134 a0001c0001t0003g0135 a0001c0001t0052g0034 |
3 | HG03139.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-293-1159C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743145 | |||||||
| chr7:1743412 | A | C | 4 | a0001c0001t0017g0084 a0001c0001t0017g0101 a0001c0001t0017g0103 others(1): Show |
4 | HG01099.hp1 HG01358.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-293-892A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743412 | |||||||
| chr7:1743488 | A | C | 1 | a0001c0001t0006g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-293-816A>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743488 | |||||||
| chr7:1743503 | T | G | 1 | a0001c0001t0016g0038 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-293-801T>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743503 | |||||||
| chr7:1743528 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-293-776A>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743528 | |||||||
| chr7:1743544 | TG | T | 3 | a0002c0003t0024g0045 a0002c0003t0024g0145 a0002c0003t0024g0182 |
3 | HG02145.hp1 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-293-756delG | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1743544 | ||||||
| chr7:1743624 | G | A | 3 | a0001c0001t0001g0244 a0001c0001t0001g0274 a0001c0001t0060g0245 |
3 | HG02135.hp1 NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-293-680G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743624 | |||||||
| chr7:1743668 | G | T | 1 | a0001c0027t0062g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-293-636G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743668 | |||||||
| chr7:1743683 | G | T | 2 | a0004c0008t0028g0284 a0004c0008t0029g0283 |
2 | HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-293-621G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743683 | |||||||
| chr7:1743689 | G | A | 1 | a0001c0001t0005g0285 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-293-615G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743689 | |||||||
| chr7:1743737 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(101): Show |
104 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.-293-567G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743737 | |||||||
| chr7:1743737 | G | T | 1 | a0001c0002t0003g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-293-567G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743737 | |||||||
| chr7:1743761 | C | G | 1 | a0001c0027t0062g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-293-543C>G | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743761 | |||||||
| chr7:1743769 | G | A | 5 | a0001c0001t0026g0136 a0001c0005t0010g0004 a0001c0005t0010g0142 others(2): Show |
6 | HG02622.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-293-535G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743769 | |||||||
| chr7:1743853 | G | A | 1 | a0001c0001t0004g0205 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-293-451G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743853 | |||||||
| chr7:1743946 | C | T | 1 | a0001c0001t0009g0120 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-293-358C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1743946 | |||||||
| chr7:1744022 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0053 a0001c0001t0001g0154 |
3 | HG02451.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-293-282C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744022 | |||||||
| chr7:1744118 | GA | G | 4 | a0001c0001t0008g0029 a0001c0001t0008g0124 a0001c0001t0008g0132 others(1): Show |
4 | HG02615.hp2 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-293-185delA | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744118 | |||||||
| chr7:1744145 | G | A | 45 | a0001c0001t0001g0069 a0001c0001t0001g0117 a0001c0001t0004g0204 others(42): Show |
46 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.-293-159G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744145 | |||||||
| chr7:1744215 | G | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(287): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.-293-89G>C | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744215 | |||||||
| chr7:1744215 | G | T | 1 | a0001c0002t0003g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-293-89G>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744215 | |||||||
| chr7:1744222 | C | T | 1 | a0001c0001t0021g0268 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-293-82C>T | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744222 | |||||||
| chr7:1744242 | CGTCCCCT others(19): Show |
C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(96): Show |
100 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(97): Show |
splice_region_variant&intron_variant | LOW | c.-293-32_-293-7delC others(25): Show |
ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr7 | 1744242 | ||||||
| chr7:1744280 | G | A | 11 | a0001c0001t0005g0035 a0001c0001t0005g0056 a0001c0001t0005g0149 others(8): Show |
11 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-293-24G>A | ELFN1 | ENSG00000225968.8 | transcript | ENST00000424383.5 | protein_coding | 3/3 | chr7 | 1744280 |