Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 114794 |
| ensemblid | ENSG00000166897.16 |
| hgncid | 29396 |
| symbol | ELFN2 |
| name | extracellular leucine rich repeat and fibronectin type III domain containing 2 |
| refseq_nuc | NM_052906.5 |
| refseq_prot | NP_443138.2 |
| ensembl_nuc | ENST00000402918.7 |
| ensembl_prot | ENSP00000385277.1 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 37367960 |
| end | 37427479 |
| strand | - |
| ver | v1.2 |
| region | chr22:37367960-37427479 |
| region5000 | chr22:37362960-37432479 |
| regionname0 | ELFN2_chr22_37367960_37427479 |
| regionname5000 | ELFN2_chr22_37362960_37432479 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 820 | 326 | 92 | 56 | 123 | 15 | 38 | 78 | ELFN2_chr22_37362960_37432479 | ELFN2 | MLRLG others(815): Show |
chr22 | 37362960 | 37432479 |
| a0002 | 0/0 | 820 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | MLRLG others(815): Show |
chr22 | 37362960 | 37432479 |
| a0003 | 0/0 | 820 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | MLRLG others(815): Show |
chr22 | 37362960 | 37432479 |
| a0004 | 0/0 | 820 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | MLRLG others(815): Show |
chr22 | 37362960 | 37432479 |
| a0005 | 0/0 | 820 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | MLRLG others(815): Show |
chr22 | 37362960 | 37432479 |
| a0006 | 0/0 | 820 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | MLRLG others(815): Show |
chr22 | 37362960 | 37432479 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2460 | 118 | 37 | 23 | 43 | 6 | 9 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0002 | 0/1 | 2460 | 104 | 21 | 18 | 47 | 3 | 14 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0003 | 1/0 | 2460 | 71 | 14 | 9 | 30 | 3 | 14 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0004 | 0/0 | 2460 | 6 | 0 | 3 | 0 | 3 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0005 | 0/0 | 2460 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0006 | 0/0 | 2460 | 5 | 3 | 1 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0008 | 0/0 | 2460 | 4 | 4 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0009 | 0/0 | 2460 | 4 | 1 | 1 | 1 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0010 | 0/0 | 2460 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0011 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0013 | 0/0 | 2460 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0015 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0018 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0019 | 0/0 | 2460 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0001c0020 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0002c0007 | 0/0 | 2460 | 4 | 4 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0003c0017 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0004c0012 | 0/0 | 2460 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0005c0016 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 | ||
| a0006c0014 | 0/0 | 2460 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | ATGCT others(2455): Show |
chr22 | 37362960 | 37432479 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 8372 | 30 | 0 | 3 | 25 | 1 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0003 | 0/0 | 8369 | 28 | 2 | 15 | 1 | 3 | 7 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0005 | 0/0 | 8369 | 16 | 16 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0009 | 0/0 | 8369 | 7 | 6 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0017 | 0/0 | 8365 | 3 | 2 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8360): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0019 | 0/0 | 8372 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0023 | 0/0 | 8372 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0024 | 0/0 | 8378 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8373): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0025 | 0/0 | 8374 | 2 | 1 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8369): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0026 | 0/0 | 8375 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8370): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0027 | 0/0 | 8371 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8366): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0028 | 0/0 | 8372 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0029 | 0/0 | 8372 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0030 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8363): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0050 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8366): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0051 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0052 | 0/0 | 8372 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0053 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0057 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0058 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0060 | 0/0 | 8365 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8360): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0061 | 0/0 | 8365 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8360): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0062 | 0/0 | 8366 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8361): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0063 | 0/0 | 8362 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8357): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0064 | 0/0 | 8363 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8358): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0065 | 0/0 | 8363 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8358): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0096 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0097 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8363): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0098 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0001t0099 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0004 | 0/0 | 8372 | 26 | 3 | 3 | 11 | 3 | 6 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0006 | 0/1 | 8372 | 13 | 0 | 5 | 4 | 0 | 3 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0007 | 0/0 | 8369 | 11 | 0 | 1 | 7 | 0 | 3 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0008 | 0/0 | 8369 | 9 | 2 | 1 | 6 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0013 | 0/0 | 8372 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0014 | 0/0 | 8369 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0018 | 0/0 | 8372 | 3 | 1 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0021 | 0/0 | 8369 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0022 | 0/0 | 8365 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8360): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0031 | 0/0 | 8372 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0032 | 0/0 | 8372 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0033 | 0/0 | 8372 | 2 | 0 | 0 | 1 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0036 | 0/0 | 8369 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0037 | 0/0 | 8369 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0039 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0040 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0066 | 0/0 | 8378 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8373): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0067 | 0/0 | 8378 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8373): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0068 | 0/0 | 8378 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8373): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0069 | 0/0 | 8378 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8373): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0071 | 0/0 | 8373 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8368): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0074 | 0/0 | 8371 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8366): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0075 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0076 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0077 | 0/0 | 8372 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0078 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0079 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0082 | 0/0 | 8369 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0084 | 0/0 | 8370 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0088 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8363): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0089 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0090 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0091 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0002t0095 | 0/0 | 8369 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0001 | 1/0 | 8370 | 45 | 6 | 7 | 25 | 1 | 5 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0006 | 0/0 | 8372 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0012 | 0/0 | 8370 | 4 | 0 | 0 | 0 | 1 | 3 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0020 | 0/0 | 8370 | 3 | 0 | 0 | 3 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0034 | 0/0 | 8370 | 2 | 0 | 0 | 0 | 0 | 2 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0035 | 0/0 | 8370 | 2 | 1 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0038 | 0/0 | 8373 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8368): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0041 | 0/0 | 8380 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8375): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0042 | 0/0 | 8377 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8372): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0043 | 0/0 | 8377 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8372): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0044 | 0/0 | 8378 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8373): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0070 | 0/0 | 8376 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8371): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0073 | 0/0 | 8373 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8368): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0081 | 0/0 | 8370 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0083 | 0/0 | 8369 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0085 | 0/0 | 8370 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0087 | 0/0 | 8370 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0092 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0093 | 0/0 | 8369 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0003t0094 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0004t0010 | 0/0 | 8373 | 6 | 0 | 3 | 0 | 3 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8368): Show |
chr22 | 37362960 | 37432479 |
| a0001c0005t0011 | 0/0 | 8372 | 5 | 5 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0006t0001 | 0/0 | 8370 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0006t0047 | 0/0 | 8375 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8370): Show |
chr22 | 37362960 | 37432479 |
| a0001c0006t0048 | 0/0 | 8375 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8370): Show |
chr22 | 37362960 | 37432479 |
| a0001c0006t0054 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0006t0056 | 0/0 | 8369 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0008t0015 | 0/0 | 8375 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8370): Show |
chr22 | 37362960 | 37432479 |
| a0001c0008t0046 | 0/0 | 8375 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8370): Show |
chr22 | 37362960 | 37432479 |
| a0001c0009t0002 | 0/0 | 8372 | 2 | 0 | 1 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0009t0049 | 0/0 | 8373 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8368): Show |
chr22 | 37362960 | 37432479 |
| a0001c0009t0055 | 0/0 | 8369 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8364): Show |
chr22 | 37362960 | 37432479 |
| a0001c0010t0016 | 0/0 | 8371 | 3 | 3 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8366): Show |
chr22 | 37362960 | 37432479 |
| a0001c0011t0059 | 0/0 | 8365 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8360): Show |
chr22 | 37362960 | 37432479 |
| a0001c0013t0012 | 0/0 | 8370 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0001c0015t0080 | 0/0 | 8372 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0001c0018t0045 | 0/0 | 8374 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8369): Show |
chr22 | 37362960 | 37432479 |
| a0001c0019t0030 | 0/0 | 8368 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8363): Show |
chr22 | 37362960 | 37432479 |
| a0001c0020t0002 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0002c0007t0001 | 0/0 | 8370 | 2 | 2 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0002c0007t0072 | 0/0 | 8373 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8368): Show |
chr22 | 37362960 | 37432479 |
| a0002c0007t0086 | 0/0 | 8370 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0003c0017t0002 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0004c0012t0001 | 0/0 | 8370 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8365): Show |
chr22 | 37362960 | 37432479 |
| a0005c0016t0002 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| a0006c0014t0004 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | GTCTG others(8367): Show |
chr22 | 37362960 | 37432479 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0017g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0017g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0017g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0019g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0019g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0019g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0023g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0023g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0024g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0024g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0025g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0025g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0026g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0026g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0027g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0027g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0028g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0028g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0029g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0029g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0030g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0050g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0051g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0052g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0053g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0057g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0058g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0060g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0061g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0062g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0063g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0064g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0065g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0096g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0097g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0098g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0001t0099g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0236 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0006g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0007g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0013g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0013g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0013g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0014g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0014g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0014g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0018g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0018g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0021g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0021g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0021g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0022g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0022g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0022g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0031g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0031g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0032g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0032g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0033g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0033g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0036g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0036g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0037g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0037g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0039g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0040g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0066g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0067g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0068g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0069g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0071g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0074g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0075g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0076g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0077g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0078g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0079g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0082g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0084g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0088g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0089g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0090g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0091g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0002t0095g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0006g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0012g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0012g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0012g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0012g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0020g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0020g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0020g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0034g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0035g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0035g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0038g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0041g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0042g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0043g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0044g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0070g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0073g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0081g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0083g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0085g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0087g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0092g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0093g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0003t0094g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0004t0010g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0005t0011g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0005t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0005t0011g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0005t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0005t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0006t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0006t0047g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0006t0048g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0006t0054g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0006t0056g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0008t0015g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0008t0015g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0008t0015g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0008t0046g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0009t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0009t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0009t0049g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0009t0055g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0010t0016g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0010t0016g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0010t0016g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0011t0059g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0013t0012g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0015t0080g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0018t0045g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0019t0030g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0001c0020t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0002c0007t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0002c0007t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0002c0007t0072g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0002c0007t0086g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0003c0017t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0004c0012t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0005c0016t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| a0006c0014t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0035 | g0057 | EUR | GBR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00099 | hp2 | a0001 | c0001 | t0058 | g0193 | EUR | GBR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00140 | hp1 | a0001 | c0003 | t0012 | g0245 | EUR | GBR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0238 | EUR | GBR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0296 | EUR | FIN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0308 | EUR | FIN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00408 | hp1 | a0001 | c0003 | t0020 | g0115 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00408 | hp2 | a0001 | c0002 | t0007 | g0130 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00423 | hp2 | a0001 | c0002 | t0007 | g0206 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00438 | hp1 | a0001 | c0003 | t0001 | g0103 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00438 | hp2 | a0003 | c0017 | t0002 | g0048 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00544 | hp2 | a0001 | c0002 | t0004 | g0298 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00558 | hp2 | a0001 | c0006 | t0001 | g0275 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00597 | hp1 | a0001 | c0003 | t0020 | g0035 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00597 | hp2 | a0001 | c0002 | t0004 | g0293 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00609 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00621 | hp1 | a0001 | c0002 | t0004 | g0016 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00621 | hp2 | a0001 | c0001 | t0029 | g0096 | EAS | CHS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00639 | hp1 | a0001 | c0002 | t0007 | g0304 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0211 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0028 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00642 | hp2 | a0001 | c0002 | t0004 | g0192 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00733 | hp1 | a0001 | c0004 | t0010 | g0300 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0092 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0125 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01081 | hp1 | a0001 | c0002 | t0071 | g0069 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01081 | hp2 | a0001 | c0002 | t0006 | g0260 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01099 | hp1 | a0001 | c0002 | t0069 | g0142 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01099 | hp2 | a0001 | c0004 | t0010 | g0310 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0065 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01109 | hp1 | a0001 | c0001 | t0062 | g0159 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01109 | hp2 | a0001 | c0002 | t0008 | g0232 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01167 | hp1 | a0001 | c0003 | t0006 | g0121 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01168 | hp1 | a0001 | c0003 | t0081 | g0183 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01168 | hp2 | a0001 | c0002 | t0006 | g0271 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01169 | hp1 | a0001 | c0002 | t0006 | g0250 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01175 | hp1 | a0001 | c0002 | t0004 | g0144 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0061 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0124 | AMR | PUR | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01255 | hp1 | a0001 | c0013 | t0012 | g0064 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01256 | hp1 | a0001 | c0002 | t0006 | g0269 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01256 | hp2 | a0001 | c0002 | t0037 | g0110 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01257 | hp2 | a0001 | c0002 | t0031 | g0175 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01258 | hp1 | a0001 | c0002 | t0006 | g0268 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01258 | hp2 | a0001 | c0002 | t0031 | g0176 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01261 | hp1 | a0001 | c0002 | t0018 | g0001 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0055 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01346 | hp2 | a0001 | c0002 | t0018 | g0001 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01358 | hp2 | a0001 | c0001 | t0099 | g0328 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01361 | hp1 | a0001 | c0002 | t0037 | g0113 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0118 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01433 | hp2 | a0001 | c0001 | t0025 | g0239 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01496 | hp1 | a0001 | c0006 | t0056 | g0221 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | CLM | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01515 | hp1 | a0004 | c0012 | t0001 | g0243 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01515 | hp2 | a0001 | c0004 | t0010 | g0180 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01516 | hp1 | a0001 | c0001 | t0017 | g0316 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0244 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01517 | hp1 | a0001 | c0004 | t0010 | g0246 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0179 | EUR | IBS | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01884 | hp1 | a0001 | c0006 | t0054 | g0022 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01891 | hp1 | a0001 | c0010 | t0016 | g0292 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01891 | hp2 | a0001 | c0005 | t0011 | g0197 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01928 | hp2 | a0001 | c0009 | t0002 | g0264 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02015 | hp1 | a0001 | c0001 | t0026 | g0289 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02015 | hp2 | a0001 | c0003 | t0001 | g0026 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02027 | hp1 | a0001 | c0002 | t0095 | g0098 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02027 | hp2 | a0001 | c0002 | t0004 | g0085 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0158 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02055 | hp2 | a0001 | c0006 | t0047 | g0204 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02056 | hp1 | a0001 | c0002 | t0014 | g0033 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02056 | hp2 | a0001 | c0001 | t0051 | g0027 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02071 | hp2 | a0001 | c0002 | t0013 | g0076 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02074 | hp1 | a0001 | c0020 | t0002 | g0253 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02080 | hp2 | a0001 | c0002 | t0004 | g0190 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0068 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02129 | hp2 | a0001 | c0002 | t0004 | g0286 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02132 | hp1 | a0001 | c0002 | t0013 | g0075 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02132 | hp2 | a0001 | c0002 | t0004 | g0259 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02145 | hp1 | a0001 | c0010 | t0016 | g0284 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0178 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02148 | hp1 | a0001 | c0001 | t0057 | g0195 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02148 | hp2 | a0001 | c0004 | t0010 | g0073 | AMR | PEL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02155 | hp1 | a0001 | c0002 | t0004 | g0174 | EAS | CDX | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0273 | EAS | CDX | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02165 | hp1 | a0001 | c0002 | t0007 | g0117 | EAS | CDX | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02165 | hp2 | a0001 | c0002 | t0032 | g0039 | EAS | CDX | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0203 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02257 | hp2 | a0001 | c0003 | t0035 | g0058 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02258 | hp1 | a0001 | c0002 | t0088 | g0285 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0306 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02280 | hp1 | a0001 | c0001 | t0063 | g0322 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02280 | hp2 | a0002 | c0007 | t0001 | g0215 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02451 | hp2 | a0001 | c0005 | t0011 | g0212 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02523 | hp1 | a0001 | c0001 | t0029 | g0114 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02523 | hp2 | a0001 | c0001 | t0026 | g0059 | EAS | KHV | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02572 | hp1 | a0001 | c0002 | t0021 | g0134 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02572 | hp2 | a0001 | c0001 | t0030 | g0153 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02602 | hp1 | a0001 | c0002 | t0004 | g0089 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02602 | hp2 | a0001 | c0001 | t0052 | g0116 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0147 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02615 | hp2 | a0001 | c0008 | t0015 | g0161 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02622 | hp1 | a0001 | c0001 | t0050 | g0146 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0168 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02630 | hp1 | a0001 | c0003 | t0070 | g0167 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02630 | hp2 | a0001 | c0003 | t0001 | g0150 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02647 | hp1 | a0001 | c0001 | t0027 | g0205 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02717 | hp1 | a0001 | c0019 | t0030 | g0127 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02717 | hp2 | a0001 | c0003 | t0083 | g0220 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02723 | hp2 | a0001 | c0002 | t0036 | g0166 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0272 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0084 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02738 | hp1 | a0001 | c0002 | t0007 | g0186 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0018 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02809 | hp1 | a0001 | c0008 | t0046 | g0163 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02809 | hp2 | a0001 | c0018 | t0045 | g0173 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02818 | hp1 | a0001 | c0001 | t0060 | g0227 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02818 | hp2 | a0001 | c0002 | t0067 | g0234 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0228 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02886 | hp2 | a0002 | c0007 | t0072 | g0320 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02895 | hp1 | a0001 | c0002 | t0066 | g0233 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02896 | hp1 | a0001 | c0002 | t0077 | g0160 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02896 | hp2 | a0001 | c0003 | t0001 | g0201 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0202 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02922 | hp2 | a0001 | c0005 | t0011 | g0213 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02965 | hp1 | a0001 | c0002 | t0068 | g0133 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0151 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0155 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02970 | hp2 | a0001 | c0002 | t0021 | g0198 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02976 | hp1 | a0001 | c0001 | t0064 | g0305 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03017 | hp1 | a0001 | c0002 | t0007 | g0185 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0063 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03041 | hp1 | a0001 | c0010 | t0016 | g0291 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0226 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03098 | hp1 | a0002 | c0007 | t0086 | g0313 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0169 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0156 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0324 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03195 | hp1 | a0001 | c0011 | t0059 | g0219 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0128 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03209 | hp1 | a0001 | c0002 | t0022 | g0157 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03209 | hp2 | a0001 | c0003 | t0041 | g0164 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03225 | hp1 | a0001 | c0001 | t0027 | g0217 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03225 | hp2 | a0002 | c0007 | t0001 | g0216 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03239 | hp1 | a0001 | c0002 | t0006 | g0262 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03239 | hp2 | a0001 | c0003 | t0092 | g0319 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03453 | hp1 | a0001 | c0008 | t0015 | g0171 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03486 | hp1 | a0001 | c0006 | t0048 | g0132 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0139 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03490 | hp2 | a0001 | c0003 | t0034 | g0006 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0282 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03491 | hp2 | a0001 | c0003 | t0012 | g0290 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03492 | hp1 | a0001 | c0003 | t0034 | g0006 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0261 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03516 | hp1 | a0001 | c0005 | t0011 | g0214 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0172 | AFR | ESN | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03540 | hp1 | a0001 | c0001 | t0097 | g0321 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03540 | hp2 | a0001 | c0002 | t0082 | g0317 | AFR | GWD | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0149 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03579 | hp2 | a0001 | c0001 | t0061 | g0184 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03654 | hp1 | a0001 | c0002 | t0004 | g0012 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0024 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03688 | hp2 | a0001 | c0003 | t0012 | g0062 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0141 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03704 | hp2 | a0001 | c0002 | t0004 | g0249 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03710 | hp1 | a0001 | c0003 | t0094 | g0011 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0029 | SAS | PJL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03831 | hp1 | a0001 | c0002 | t0007 | g0191 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03831 | hp2 | a0001 | c0003 | t0001 | g0138 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03834 | hp1 | a0001 | c0002 | t0006 | g0137 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03834 | hp2 | a0001 | c0002 | t0033 | g0025 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03927 | hp1 | a0001 | c0009 | t0055 | g0015 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03927 | hp2 | a0001 | c0003 | t0073 | g0014 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04115 | hp1 | a0001 | c0002 | t0006 | g0247 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04115 | hp2 | a0001 | c0003 | t0012 | g0303 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04184 | hp2 | a0001 | c0003 | t0085 | g0187 | SAS | BEB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04228 | hp1 | a0001 | c0002 | t0089 | g0131 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG04228 | hp2 | a0001 | c0002 | t0004 | g0143 | SAS | STU | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18522 | hp1 | a0001 | c0002 | t0036 | g0318 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18522 | hp2 | a0001 | c0005 | t0011 | g0208 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18612 | hp1 | a0001 | c0002 | t0033 | g0199 | EAS | CHB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18612 | hp2 | a0001 | c0001 | t0023 | g0077 | EAS | CHB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18747 | hp1 | a0001 | c0003 | t0001 | g0038 | EAS | CHB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18906 | hp1 | a0001 | c0003 | t0042 | g0230 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18906 | hp2 | a0001 | c0002 | t0074 | g0224 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0109 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18939 | hp2 | a0001 | c0003 | t0001 | g0030 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18941 | hp1 | a0001 | c0002 | t0007 | g0106 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18941 | hp2 | a0001 | c0003 | t0020 | g0041 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18943 | hp1 | a0001 | c0001 | t0053 | g0090 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18943 | hp2 | a0001 | c0002 | t0008 | g0093 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0263 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18945 | hp1 | a0001 | c0002 | t0090 | g0309 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18948 | hp1 | a0001 | c0001 | t0096 | g0053 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18948 | hp2 | a0005 | c0016 | t0002 | g0257 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18949 | hp1 | a0001 | c0002 | t0008 | g0049 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18949 | hp2 | a0001 | c0002 | t0039 | g0009 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18950 | hp1 | a0001 | c0001 | t0019 | g0108 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18950 | hp2 | a0001 | c0002 | t0079 | g0237 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18952 | hp1 | a0001 | c0002 | t0004 | g0023 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18952 | hp2 | a0001 | c0003 | t0087 | g0295 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18960 | hp1 | a0001 | c0001 | t0023 | g0120 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18960 | hp2 | a0001 | c0002 | t0014 | g0080 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18962 | hp1 | a0001 | c0003 | t0038 | g0074 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18962 | hp2 | a0001 | c0002 | t0006 | g0095 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18964 | hp1 | a0001 | c0001 | t0024 | g0256 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18964 | hp2 | a0001 | c0002 | t0008 | g0051 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18966 | hp1 | a0001 | c0002 | t0084 | g0050 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18967 | hp1 | a0001 | c0002 | t0078 | g0104 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18968 | hp1 | a0001 | c0002 | t0091 | g0054 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18969 | hp2 | a0001 | c0003 | t0001 | g0082 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0100 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18973 | hp2 | a0001 | c0002 | t0014 | g0078 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18975 | hp2 | a0001 | c0002 | t0006 | g0196 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18980 | hp1 | a0001 | c0003 | t0001 | g0097 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18981 | hp1 | a0001 | c0002 | t0007 | g0071 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18981 | hp2 | a0001 | c0002 | t0008 | g0081 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18983 | hp1 | a0001 | c0001 | t0098 | g0327 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18983 | hp2 | a0001 | c0001 | t0019 | g0107 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18986 | hp1 | a0001 | c0009 | t0002 | g0112 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18986 | hp2 | a0001 | c0003 | t0001 | g0297 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18991 | hp1 | a0001 | c0002 | t0075 | g0088 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18991 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0099 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18995 | hp2 | a0001 | c0002 | t0008 | g0188 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18998 | hp1 | a0001 | c0002 | t0008 | g0056 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19000 | hp2 | a0001 | c0001 | t0028 | g0274 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19005 | hp1 | a0001 | c0003 | t0001 | g0002 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19005 | hp2 | a0001 | c0001 | t0019 | g0254 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19012 | hp1 | a0001 | c0001 | t0028 | g0307 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19030 | hp1 | a0001 | c0001 | t0017 | g0209 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0288 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19043 | hp2 | a0001 | c0002 | t0018 | g0177 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19056 | hp2 | a0001 | c0002 | t0006 | g0276 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19058 | hp1 | a0001 | c0002 | t0076 | g0037 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19058 | hp2 | a0001 | c0003 | t0001 | g0235 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19065 | hp1 | a0001 | c0001 | t0024 | g0255 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19066 | hp1 | a0001 | c0002 | t0032 | g0299 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19068 | hp1 | a0001 | c0002 | t0004 | g0040 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19068 | hp2 | a0001 | c0002 | t0007 | g0072 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0083 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19080 | hp1 | a0001 | c0002 | t0040 | g0010 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19085 | hp2 | a0001 | c0002 | t0013 | g0079 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19088 | hp1 | a0001 | c0002 | t0006 | g0181 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19088 | hp2 | a0001 | c0002 | t0004 | g0036 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19089 | hp1 | a0006 | c0014 | t0004 | g0034 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19089 | hp2 | a0001 | c0002 | t0007 | g0091 | EAS | JPT | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19240 | hp1 | a0001 | c0001 | t0065 | g0170 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | YRI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20129 | hp1 | a0001 | c0003 | t0044 | g0326 | AFR | ASW | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20129 | hp2 | a0001 | c0003 | t0043 | g0231 | AFR | ASW | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0283 | EUR | TSI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0200 | EUR | TSI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20805 | hp1 | a0001 | c0004 | t0010 | g0302 | EUR | TSI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20805 | hp2 | a0001 | c0002 | t0004 | g0251 | EUR | TSI | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | GIH | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0225 | SAS | GIH | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02109 | hp1 | a0001 | c0008 | t0015 | g0162 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02109 | hp2 | a0001 | c0002 | t0004 | g0325 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02486 | hp1 | a0001 | c0002 | t0022 | g0314 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02486 | hp2 | a0001 | c0015 | t0080 | g0223 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02559 | hp1 | a0001 | c0002 | t0008 | g0312 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG02559 | hp2 | a0001 | c0001 | t0025 | g0323 | AFR | ACB | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03471 | hp1 | a0001 | c0002 | t0008 | g0229 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | MSL | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20300 | hp1 | a0001 | c0009 | t0049 | g0287 | AFR | USA | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA20300 | hp2 | a0001 | c0002 | t0021 | g0148 | AFR | USA | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA21309 | hp1 | a0001 | c0003 | t0093 | g0315 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| NA21309 | hp2 | a0001 | c0002 | t0022 | g0311 | AFR | LWK | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0006 | g0236 | REF | REF | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0145 | REF | REF | ELFN2_chr22_37362960_37432479 | ELFN2 | chr22 | 37362960 | 37432479 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37373356 | G | A | 1 | a0004 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2179C>T | p.Arg727Cys | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2974/8370 | 2179/2463 | 727/820 | chr22 | 37373356 | |||
| chr22:37373455 | T | C | 1 | a0006 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.2080A>G | p.Ile694Val | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2875/8370 | 2080/2463 | 694/820 | chr22 | 37373455 | |||
| chr22:37373646 | C | T | 1 | a0003 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.1889G>A | p.Ser630Asn | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2684/8370 | 1889/2463 | 630/820 | chr22 | 37373646 | |||
| chr22:37373983 | C | T | 1 | a0005 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.1552G>A | p.Glu518Lys | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2347/8370 | 1552/2463 | 518/820 | chr22 | 37373983 | |||
| chr22:37374750 | G | T | 1 | a0002 | 4 | HG02280.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
missense_variant | MODERATE | c.785C>A | p.Ser262Tyr | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1580/8370 | 785/2463 | 262/820 | chr22 | 37374750 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37373672 | G | A | 1 | a0001c0010 | 3 | HG01891.hp1 HG02145.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.1863C>T | p.Asp621Asp | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2658/8370 | 1863/2463 | 621/820 | chr22 | 37373672 | |||
| chr22:37374008 | G | A | 1 | a0001c0013 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.1527C>T | p.Ala509Ala | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2322/8370 | 1527/2463 | 509/820 | chr22 | 37374008 | |||
| chr22:37374026 | G | T | 9 | a0001c0001 a0001c0005 a0001c0010 others(6): Show |
132 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(129): Show |
synonymous_variant | LOW | c.1509C>A | p.Ile503Ile | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2304/8370 | 1509/2463 | 503/820 | chr22 | 37374026 | |||
| chr22:37374068 | G | A | 2 | a0001c0008 a0001c0018 |
5 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
synonymous_variant | LOW | c.1467C>T | p.Ala489Ala | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2262/8370 | 1467/2463 | 489/820 | chr22 | 37374068 | |||
| chr22:37374170 | G | A | 1 | a0001c0008 | 4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.1365C>T | p.Ala455Ala | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2160/8370 | 1365/2463 | 455/820 | chr22 | 37374170 | |||
| chr22:37374317 | A | G | 12 | a0001c0001 a0001c0005 a0001c0006 others(9): Show |
145 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(142): Show |
synonymous_variant | LOW | c.1218T>C | p.Phe406Phe | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2013/8370 | 1218/2463 | 406/820 | chr22 | 37374317 | |||
| chr22:37374590 | G | A | 3 | a0001c0002 a0001c0015 a0006c0014 |
105 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(102): Show |
synonymous_variant | LOW | c.945C>T | p.Ile315Ile | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1740/8370 | 945/2463 | 315/820 | chr22 | 37374590 | |||
| chr22:37374743 | G | A | 1 | a0001c0019 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.792C>T | p.Asp264Asp | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1587/8370 | 792/2463 | 264/820 | chr22 | 37374743 | |||
| chr22:37374905 | G | A | 1 | a0001c0020 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.630C>T | p.Tyr210Tyr | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1425/8370 | 630/2463 | 210/820 | chr22 | 37374905 | |||
| chr22:37375100 | G | A | 1 | a0001c0015 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.435C>T | p.Thr145Thr | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1230/8370 | 435/2463 | 145/820 | chr22 | 37375100 | |||
| chr22:37375118 | G | A | 10 | a0001c0001 a0001c0004 a0001c0009 others(7): Show |
137 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(134): Show |
synonymous_variant | LOW | c.417C>T | p.Ile139Ile | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1212/8370 | 417/2463 | 139/820 | chr22 | 37375118 | |||
| chr22:37375328 | G | T | 1 | a0001c0011 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.207C>A | p.Ala69Ala | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1002/8370 | 207/2463 | 69/820 | chr22 | 37375328 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37368100 | G | C | 1 | a0001c0002t0021 | 3 | HG02572.hp1 HG02970.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4972C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4972 | chr22 | 37368100 | ||||||
| chr22:37368114 | C | A | 1 | a0001c0001t0017 | 3 | HG01516.hp1 HG03195.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4958G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4958 | chr22 | 37368114 | ||||||
| chr22:37368173 | C | T | 3 | a0001c0001t0009 a0001c0002t0077 a0001c0006t0054 |
9 | HG00639.hp2 HG01884.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4899G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4899 | chr22 | 37368173 | ||||||
| chr22:37368213 | T | C | 43 | a0001c0001t0017 a0001c0001t0027 a0001c0001t0028 others(40): Show |
116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*4859A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4859 | chr22 | 37368213 | ||||||
| chr22:37368299 | G | A | 1 | a0001c0003t0094 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4773C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4773 | chr22 | 37368299 | ||||||
| chr22:37368310 | C | T | 1 | a0001c0002t0021 | 3 | HG02572.hp1 HG02970.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4762G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4762 | chr22 | 37368310 | ||||||
| chr22:37368363 | T | G | 1 | a0001c0002t0021 | 3 | HG02572.hp1 HG02970.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4709A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4709 | chr22 | 37368363 | ||||||
| chr22:37368383 | G | A | 8 | a0001c0002t0066 a0001c0002t0067 a0001c0003t0081 others(5): Show |
10 | HG01168.hp1 HG02109.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4689C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4689 | chr22 | 37368383 | ||||||
| chr22:37368474 | G | C | 1 | a0001c0001t0027 | 2 | HG02647.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4598C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4598 | chr22 | 37368474 | ||||||
| chr22:37368527 | C | G | 82 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0017 others(79): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*4545G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4545 | chr22 | 37368527 | ||||||
| chr22:37368572 | G | A | 1 | a0001c0002t0089 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4500C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4500 | chr22 | 37368572 | ||||||
| chr22:37368596 | C | T | 1 | a0001c0003t0020 | 3 | HG00408.hp1 HG00597.hp1 NA18941.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4476G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4476 | chr22 | 37368596 | ||||||
| chr22:37368647 | C | T | 1 | a0001c0001t0019 | 3 | NA18950.hp1 NA18983.hp2 NA19005.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4425G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4425 | chr22 | 37368647 | ||||||
| chr22:37368845 | C | A | 1 | a0001c0002t0067 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4227G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4227 | chr22 | 37368845 | ||||||
| chr22:37368854 | C | T | 6 | a0001c0001t0065 a0001c0002t0006 a0001c0002t0031 others(3): Show |
18 | HG01081.hp2 HG01167.hp1 HG01168.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4218G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4218 | chr22 | 37368854 | ||||||
| chr22:37368930 | T | C | 1 | a0002c0007t0086 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4142A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4142 | chr22 | 37368930 | ||||||
| chr22:37368975 | C | G | 1 | a0001c0001t0051 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4097G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4097 | chr22 | 37368975 | ||||||
| chr22:37369002 | T | C | 1 | a0001c0002t0021 | 3 | HG02572.hp1 HG02970.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4070A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 4070 | chr22 | 37369002 | ||||||
| chr22:37369117 | C | T | 2 | a0001c0002t0066 a0001c0002t0067 |
2 | HG02818.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3955G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3955 | chr22 | 37369117 | ||||||
| chr22:37369158 | C | T | 1 | a0001c0002t0031 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3914G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3914 | chr22 | 37369158 | ||||||
| chr22:37369232 | C | A | 2 | a0001c0002t0036 a0001c0002t0082 |
3 | HG02723.hp2 HG03540.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3840G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3840 | chr22 | 37369232 | ||||||
| chr22:37369335 | C | G | 1 | a0001c0002t0090 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3737G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3737 | chr22 | 37369335 | ||||||
| chr22:37369444 | C | T | 1 | a0001c0001t0057 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3628G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3628 | chr22 | 37369444 | ||||||
| chr22:37369464 | G | A | 1 | a0001c0003t0073 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3608C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3608 | chr22 | 37369464 | ||||||
| chr22:37369542 | C | T | 7 | a0001c0002t0066 a0001c0002t0067 a0001c0003t0092 others(4): Show |
9 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3530G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3530 | chr22 | 37369542 | ||||||
| chr22:37369843 | C | T | 1 | a0001c0003t0092 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3229G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3229 | chr22 | 37369843 | ||||||
| chr22:37369903 | T | C | 1 | a0001c0001t0064 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3169A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3169 | chr22 | 37369903 | ||||||
| chr22:37370000 | G | A | 1 | a0001c0002t0078 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3072C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3072 | chr22 | 37370000 | ||||||
| chr22:37370027 | G | A | 43 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0060 others(40): Show |
118 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*3045C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3045 | chr22 | 37370027 | ||||||
| chr22:37370048 | A | C | 14 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0060 others(11): Show |
34 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3024T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3024 | chr22 | 37370048 | ||||||
| chr22:37370053 | T | C | 1 | a0001c0002t0079 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3019A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 3019 | chr22 | 37370053 | ||||||
| chr22:37370088 | G | A | 1 | a0001c0006t0047 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2984C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2984 | chr22 | 37370088 | ||||||
| chr22:37370156 | T | C | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0019 others(20): Show |
87 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2916A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2916 | chr22 | 37370156 | ||||||
| chr22:37370284 | G | A | 3 | a0001c0008t0015 a0001c0008t0046 a0001c0011t0059 |
5 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2788C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2788 | chr22 | 37370284 | ||||||
| chr22:37370431 | G | T | 1 | a0001c0004t0010 | 6 | HG00733.hp1 HG01099.hp2 HG01515.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2641C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2641 | chr22 | 37370431 | ||||||
| chr22:37370504 | G | A | 1 | a0001c0002t0040 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2568C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2568 | chr22 | 37370504 | ||||||
| chr22:37370517 | C | T | 1 | a0001c0006t0054 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2555G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2555 | chr22 | 37370517 | ||||||
| chr22:37370542 | G | A | 2 | a0001c0002t0088 a0001c0018t0045 |
2 | HG02258.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2530C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2530 | chr22 | 37370542 | ||||||
| chr22:37370625 | G | A | 2 | a0001c0002t0022 a0001c0003t0083 |
4 | HG02486.hp1 HG02717.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2447C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2447 | chr22 | 37370625 | ||||||
| chr22:37370653 | A | G | 49 | a0001c0001t0017 a0001c0001t0028 a0001c0001t0060 others(46): Show |
126 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*2419T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2419 | chr22 | 37370653 | ||||||
| chr22:37370769 | C | T | 6 | a0001c0001t0065 a0001c0002t0006 a0001c0002t0031 others(3): Show |
19 | HG01081.hp2 HG01167.hp1 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2303G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2303 | chr22 | 37370769 | ||||||
| chr22:37370953 | A | G | 7 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0050 others(4): Show |
15 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2119T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2119 | chr22 | 37370953 | ||||||
| chr22:37370955 | G | C | 7 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0050 others(4): Show |
15 | HG01433.hp2 HG01891.hp2 HG02258.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2117C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2117 | chr22 | 37370955 | ||||||
| chr22:37370983 | G | C | 5 | a0001c0001t0027 a0001c0001t0050 a0001c0002t0021 others(2): Show |
8 | HG02258.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2089C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 2089 | chr22 | 37370983 | ||||||
| chr22:37371371 | G | A | 1 | a0001c0001t0065 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1701C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1701 | chr22 | 37371371 | ||||||
| chr22:37371554 | G | C | 5 | a0001c0001t0025 a0001c0001t0027 a0001c0002t0088 others(2): Show |
7 | HG01433.hp2 HG02258.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1518C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1518 | chr22 | 37371554 | ||||||
| chr22:37371732 | C | T | 1 | a0001c0003t0041 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1340G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1340 | chr22 | 37371732 | ||||||
| chr22:37371807 | TG | T | 20 | a0001c0001t0017 a0001c0001t0025 a0001c0001t0027 others(17): Show |
28 | HG01433.hp2 HG01516.hp1 HG01891.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1264delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1264 | chr22 | 37371807 | ||||||
| chr22:37371952 | G | T | 1 | a0001c0003t0034 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1120C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 1120 | chr22 | 37371952 | ||||||
| chr22:37372210 | C | T | 1 | a0001c0001t0061 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*862G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 862 | chr22 | 37372210 | ||||||
| chr22:37372230 | C | T | 1 | a0001c0011t0059 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*842G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 842 | chr22 | 37372230 | ||||||
| chr22:37372276 | T | A | 1 | a0001c0002t0095 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*796A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 796 | chr22 | 37372276 | ||||||
| chr22:37372318 | G | C | 1 | a0001c0008t0046 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*754C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 754 | chr22 | 37372318 | ||||||
| chr22:37372427 | C | T | 1 | a0001c0003t0042 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*645G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 645 | chr22 | 37372427 | ||||||
| chr22:37372455 | G | A | 1 | a0001c0001t0061 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*617C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 617 | chr22 | 37372455 | ||||||
| chr22:37372556 | C | T | 3 | a0001c0002t0066 a0001c0002t0067 a0001c0002t0068 |
3 | HG02818.hp2 HG02895.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*516G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 516 | chr22 | 37372556 | ||||||
| chr22:37372692 | C | T | 11 | a0001c0001t0017 a0001c0001t0060 a0001c0001t0061 others(8): Show |
21 | HG01516.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*380G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 380 | chr22 | 37372692 | ||||||
| chr22:37372717 | AC | A | 87 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(84): Show |
253 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*354delG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 354 | chr22 | 37372717 | ||||||
| chr22:37372761 | G | A | 1 | a0001c0002t0037 | 2 | HG01256.hp2 HG01361.hp1 |
3_prime_UTR_variant | MODIFIER | c.*311C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 311 | chr22 | 37372761 | ||||||
| chr22:37372816 | C | T | 1 | a0001c0002t0082 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*256G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 256 | chr22 | 37372816 | ||||||
| chr22:37373004 | G | T | 4 | a0001c0003t0012 a0001c0003t0034 a0001c0003t0081 others(1): Show |
8 | HG00140.hp1 HG01168.hp1 HG01255.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*68C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 68 | chr22 | 37373004 | ||||||
| chr22:37375612 | C | T | 1 | a0001c0001t0053 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 78 | chr22 | 37375612 | ||||||
| chr22:37375836 | C | CCCT | 38 | a0001c0001t0002 a0001c0001t0019 a0001c0001t0023 others(35): Show |
128 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
5_prime_UTR_variant | MODIFIER | c.-305_-303dupAGG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | ||||||
| chr22:37375836 | C | CCCTCCT | 8 | a0001c0001t0025 a0001c0001t0026 a0001c0003t0070 others(5): Show |
12 | HG01433.hp2 HG02015.hp1 HG02055.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-308_-303dupAGGAGG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | ||||||
| chr22:37375836 | C | CCCTCCTC others(2): Show |
8 | a0001c0001t0024 a0001c0002t0066 a0001c0002t0067 others(5): Show |
9 | HG01099.hp1 HG02818.hp2 HG02895.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-311_-303dupAGGAGG others(3): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | ||||||
| chr22:37375836 | C | CCCTCCTC others(5): Show |
1 | a0001c0003t0041 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-314_-303dupAGGAGG others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | ||||||
| chr22:37375836 | CCCT | C | 6 | a0001c0001t0017 a0001c0001t0060 a0001c0001t0061 others(3): Show |
10 | HG01109.hp1 HG01516.hp1 HG02486.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-305_-303delAGG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | ||||||
| chr22:37375836 | CCCTCCT | C | 3 | a0001c0001t0063 a0001c0001t0064 a0001c0001t0065 |
3 | HG02280.hp1 HG02976.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-308_-303delAGGAGG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 303 | chr22 | 37375836 | ||||||
| chr22:37375945 | A | G | 51 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(48): Show |
151 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(148): Show |
5_prime_UTR_variant | MODIFIER | c.-411T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 411 | chr22 | 37375945 | ||||||
| chr22:37375991 | T | C | 1 | a0001c0001t0096 | 1 | NA18948.hp1 | 5_prime_UTR_variant | MODIFIER | c.-457A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 3/3 | 457 | chr22 | 37375991 | ||||||
| chr22:37417780 | A | T | 6 | a0001c0001t0023 a0001c0002t0013 a0001c0002t0014 others(3): Show |
11 | HG02056.hp1 HG02071.hp2 HG02132.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-474T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/3 | 42246 | chr22 | 37417780 | ||||||
| chr22:37417885 | G | A | 1 | a0001c0001t0097 | 1 | HG03540.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-579C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/3 | chr22 | 37417885 | |||||||
| chr22:37427369 | G | A | 1 | a0001c0001t0098 | 1 | NA18983.hp1 | 5_prime_UTR_variant | MODIFIER | c.-685C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/3 | 51835 | chr22 | 37427369 | ||||||
| chr22:37427414 | G | A | 1 | a0001c0001t0099 | 1 | HG01358.hp2 | 5_prime_UTR_variant | MODIFIER | c.-730C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/3 | 51880 | chr22 | 37427414 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37376022 | G | A | 2 | a0001c0002t0031g0175 a0001c0002t0031g0176 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-462-26C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376022 | |||||||
| chr22:37376034 | T | G | 1 | a0001c0002t0004g0259 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-462-38A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376034 | |||||||
| chr22:37376067 | G | A | 4 | a0001c0001t0027g0205 a0001c0001t0027g0217 a0001c0001t0050g0146 others(1): Show |
4 | HG02622.hp1 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-71C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376067 | |||||||
| chr22:37376096 | G | A | 1 | a0001c0003t0001g0030 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-462-100C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376096 | |||||||
| chr22:37376142 | A | G | 6 | a0001c0003t0041g0164 a0001c0003t0042g0230 a0001c0003t0043g0231 others(3): Show |
6 | HG02055.hp2 HG03209.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-146T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376142 | |||||||
| chr22:37376240 | C | T | 1 | a0001c0018t0045g0173 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-462-244G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376240 | |||||||
| chr22:37376402 | T | TAC | 6 | a0001c0003t0041g0164 a0001c0003t0042g0230 a0001c0003t0043g0231 others(3): Show |
6 | HG02055.hp2 HG03209.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-408_-462-407d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376402 | |||||||
| chr22:37376402 | TAC | T | 130 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(127): Show |
132 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-462-408_-462-407d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376402 | |||||||
| chr22:37376502 | A | AAGAATTA others(32): Show |
1 | a0001c0001t0003g0225 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-462-545_-462-507d others(41): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376502 | |||||||
| chr22:37376829 | G | T | 239 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(236): Show |
242 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.-462-833C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37376829 | |||||||
| chr22:37377055 | C | G | 259 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(256): Show |
262 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.-462-1059G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377055 | |||||||
| chr22:37377470 | A | G | 2 | a0001c0006t0048g0132 a0001c0006t0056g0221 |
2 | HG01496.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-462-1474T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377470 | |||||||
| chr22:37377486 | A | T | 4 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0050g0146 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-1490T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377486 | |||||||
| chr22:37377608 | A | G | 250 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(247): Show |
253 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.-462-1612T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377608 | |||||||
| chr22:37377672 | C | T | 4 | a0001c0005t0011g0197 a0001c0005t0011g0208 a0001c0005t0011g0212 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-1676G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377672 | |||||||
| chr22:37377673 | G | A | 1 | a0001c0002t0004g0092 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-462-1677C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377673 | |||||||
| chr22:37377683 | A | G | 257 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(254): Show |
260 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.-462-1687T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377683 | |||||||
| chr22:37377967 | G | A | 2 | a0001c0001t0064g0305 a0001c0001t0065g0170 |
2 | HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-462-1971C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37377967 | |||||||
| chr22:37378004 | G | A | 107 | a0001c0001t0002g0043 a0001c0001t0002g0241 a0001c0001t0003g0044 others(104): Show |
108 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-462-2008C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378004 | |||||||
| chr22:37378045 | T | C | 138 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0052 others(135): Show |
140 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.-462-2049A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378045 | |||||||
| chr22:37378153 | G | A | 4 | a0001c0003t0041g0164 a0001c0003t0042g0230 a0001c0003t0043g0231 others(1): Show |
4 | HG03209.hp2 NA18906.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-2157C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378153 | |||||||
| chr22:37378191 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-462-2195C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378191 | |||||||
| chr22:37378200 | T | C | 2 | a0001c0003t0012g0303 a0001c0003t0034g0006 |
3 | HG03490.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-462-2204A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378200 | |||||||
| chr22:37378238 | G | T | 4 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0050g0146 others(1): Show |
4 | HG02622.hp1 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-2242C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378238 | |||||||
| chr22:37378318 | G | A | 121 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0052 others(118): Show |
123 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.-462-2322C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378318 | |||||||
| chr22:37378349 | A | C | 257 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(254): Show |
260 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.-462-2353T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378349 | |||||||
| chr22:37378500 | T | C | 257 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(254): Show |
260 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.-462-2504A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378500 | |||||||
| chr22:37378527 | A | G | 5 | a0001c0002t0004g0325 a0001c0002t0066g0233 a0001c0002t0067g0234 others(2): Show |
5 | HG01099.hp1 HG02109.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-462-2531T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378527 | |||||||
| chr22:37378628 | C | T | 2 | a0001c0001t0023g0077 a0001c0001t0023g0120 |
2 | NA18612.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.-462-2632G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378628 | |||||||
| chr22:37378703 | C | T | 5 | a0001c0002t0004g0325 a0001c0002t0066g0233 a0001c0002t0067g0234 others(2): Show |
5 | HG01099.hp1 HG02109.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-462-2707G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378703 | |||||||
| chr22:37378726 | C | T | 1 | a0001c0001t0005g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-462-2730G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378726 | |||||||
| chr22:37378766 | G | A | 36 | a0001c0001t0002g0043 a0001c0001t0002g0241 a0001c0001t0003g0272 others(33): Show |
36 | HG00423.hp2 HG00639.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.-462-2770C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378766 | |||||||
| chr22:37378784 | C | A | 1 | a0001c0001t0026g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-462-2788G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378784 | |||||||
| chr22:37378801 | G | A | 1 | a0001c0003t0087g0295 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-462-2805C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378801 | |||||||
| chr22:37378822 | G | T | 1 | a0001c0003t0083g0220 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-462-2826C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378822 | |||||||
| chr22:37378839 | G | T | 2 | a0001c0001t0027g0205 a0001c0001t0027g0217 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-2843C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378839 | |||||||
| chr22:37378853 | T | C | 5 | a0001c0002t0004g0325 a0001c0002t0066g0233 a0001c0002t0067g0234 others(2): Show |
5 | HG01099.hp1 HG02109.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-462-2857A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378853 | |||||||
| chr22:37378861 | T | C | 266 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(263): Show |
269 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.-462-2865A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37378861 | |||||||
| chr22:37379023 | C | T | 78 | a0001c0001t0003g0044 a0001c0001t0003g0067 a0001c0001t0003g0084 others(75): Show |
79 | HG00140.hp2 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-462-3027G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379023 | |||||||
| chr22:37379188 | T | G | 113 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0052 others(110): Show |
115 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-462-3192A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379188 | |||||||
| chr22:37379212 | G | A | 3 | a0001c0001t0005g0165 a0001c0001t0027g0205 a0001c0001t0027g0217 |
3 | HG02647.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-462-3216C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379212 | |||||||
| chr22:37379218 | A | G | 206 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0052 others(203): Show |
209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-462-3222T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379218 | |||||||
| chr22:37379227 | G | A | 1 | a0001c0002t0006g0196 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-462-3231C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379227 | |||||||
| chr22:37379294 | C | T | 2 | a0001c0001t0027g0205 a0001c0001t0027g0217 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-3298G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379294 | |||||||
| chr22:37379355 | G | A | 1 | a0001c0003t0070g0167 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-462-3359C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379355 | |||||||
| chr22:37379461 | C | G | 1 | a0001c0002t0032g0039 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-462-3465G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379461 | |||||||
| chr22:37379641 | C | T | 2 | a0001c0001t0005g0020 a0001c0001t0005g0021 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-462-3645G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379641 | |||||||
| chr22:37379667 | G | A | 1 | a0001c0002t0032g0039 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-462-3671C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379667 | |||||||
| chr22:37379697 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-462-3701C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379697 | |||||||
| chr22:37379718 | G | C | 2 | a0001c0001t0005g0135 a0001c0001t0005g0136 |
2 | HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-462-3722C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379718 | |||||||
| chr22:37379850 | C | T | 148 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(145): Show |
150 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.-462-3854G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379850 | |||||||
| chr22:37379852 | G | GGTGCTCC others(6): Show |
1 | a0001c0002t0008g0049 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-462-3869_-462-385 others(17): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379852 | |||||||
| chr22:37379867 | C | T | 1 | a0001c0001t0061g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-462-3871G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379867 | |||||||
| chr22:37379875 | T | C | 6 | a0001c0001t0002g0258 a0001c0001t0002g0281 a0001c0001t0002g0294 others(3): Show |
6 | NA18945.hp2 NA18964.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-3879A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379875 | |||||||
| chr22:37379934 | C | G | 252 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(249): Show |
255 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.-462-3938G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379934 | |||||||
| chr22:37379967 | C | T | 1 | a0001c0001t0023g0077 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-462-3971G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379967 | |||||||
| chr22:37379998 | G | C | 1 | a0001c0003t0006g0121 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-462-4002C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37379998 | |||||||
| chr22:37380265 | G | A | 1 | a0001c0001t0065g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-462-4269C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380265 | |||||||
| chr22:37380336 | T | TCA | 262 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(259): Show |
265 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.-462-4341_-462-434 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380336 | |||||||
| chr22:37380415 | C | T | 4 | a0001c0003t0001g0178 a0001c0003t0001g0201 a0001c0003t0001g0202 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-4419G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380415 | |||||||
| chr22:37380485 | C | G | 1 | a0001c0002t0018g0001 | 2 | HG01261.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-462-4489G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380485 | |||||||
| chr22:37380939 | T | C | 3 | a0001c0003t0001g0013 a0001c0003t0001g0030 a0001c0003t0001g0083 |
3 | NA18939.hp2 NA18991.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-462-4943A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380939 | |||||||
| chr22:37380991 | A | G | 260 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(257): Show |
263 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.-462-4995T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37380991 | |||||||
| chr22:37381067 | G | A | 2 | a0001c0001t0019g0107 a0001c0001t0019g0108 |
2 | NA18950.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-462-5071C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381067 | |||||||
| chr22:37381304 | A | G | 1 | a0001c0006t0056g0221 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-462-5308T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381304 | |||||||
| chr22:37381320 | CT | C | 233 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(230): Show |
236 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.-462-5325delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381320 | |||||||
| chr22:37381573 | T | G | 244 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(241): Show |
247 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.-462-5577A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381573 | |||||||
| chr22:37381632 | C | T | 1 | a0001c0001t0005g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-462-5636G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381632 | |||||||
| chr22:37381743 | C | T | 14 | a0001c0001t0003g0004 a0001c0001t0003g0047 a0001c0001t0003g0087 others(11): Show |
15 | HG01106.hp2 HG01255.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.-462-5747G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381743 | |||||||
| chr22:37381883 | G | A | 2 | a0001c0001t0027g0205 a0001c0001t0027g0217 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-5887C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381883 | |||||||
| chr22:37381935 | G | A | 3 | a0001c0004t0010g0073 a0001c0004t0010g0180 a0001c0004t0010g0246 |
3 | HG01515.hp2 HG01517.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-462-5939C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381935 | |||||||
| chr22:37381955 | C | CA | 19 | a0001c0002t0006g0260 a0001c0002t0007g0106 a0001c0003t0001g0002 others(16): Show |
21 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.-462-5960dupT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | |||||||
| chr22:37381955 | C | CAA | 11 | a0001c0002t0007g0130 a0001c0003t0001g0028 a0001c0003t0001g0032 others(8): Show |
12 | HG00408.hp2 HG00642.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-462-5961_-462-596 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | |||||||
| chr22:37381955 | CA | C | 6 | a0001c0002t0008g0049 a0001c0002t0008g0232 a0001c0002t0008g0312 others(3): Show |
6 | HG00323.hp2 HG01109.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-462-5960delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | |||||||
| chr22:37381955 | CAAAAAAA others(1): Show |
C | 64 | a0001c0001t0002g0043 a0001c0001t0002g0060 a0001c0001t0002g0122 others(61): Show |
65 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.-462-5967_-462-596 others(12): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | |||||||
| chr22:37381955 | CAAAAAAA others(2): Show |
C | 174 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0101 others(171): Show |
176 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.-462-5968_-462-596 others(13): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | |||||||
| chr22:37381955 | CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0002g0052 a0001c0001t0005g0135 a0001c0001t0096g0053 others(1): Show |
4 | HG02723.hp1 HG03041.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-5969_-462-596 others(14): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | |||||||
| chr22:37381955 | CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0027g0205 a0001c0001t0027g0217 a0001c0002t0008g0229 |
3 | HG02647.hp1 HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-462-5975_-462-596 others(20): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381955 | |||||||
| chr22:37381970 | AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0005g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-462-5996_-462-597 others(26): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381970 | |||||||
| chr22:37381980 | AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0025g0323 a0001c0003t0001g0150 a0001c0003t0001g0324 |
3 | HG02559.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-462-5996_-462-598 others(16): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37381980 | |||||||
| chr22:37382022 | C | G | 23 | a0001c0001t0003g0067 a0001c0001t0058g0193 a0001c0001t0099g0328 others(20): Show |
23 | HG00099.hp2 HG01168.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-462-6026G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382022 | |||||||
| chr22:37382055 | T | C | 262 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(259): Show |
265 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.-462-6059A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382055 | |||||||
| chr22:37382114 | G | A | 1 | a0001c0002t0014g0078 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-462-6118C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382114 | |||||||
| chr22:37382294 | CT | C | 231 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(228): Show |
234 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.-462-6299delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382294 | |||||||
| chr22:37382330 | T | C | 2 | a0001c0001t0027g0205 a0001c0001t0027g0217 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-6334A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382330 | |||||||
| chr22:37382396 | C | T | 1 | a0001c0002t0066g0233 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-462-6400G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382396 | |||||||
| chr22:37382433 | C | T | 233 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(230): Show |
236 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.-462-6437G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382433 | |||||||
| chr22:37382436 | G | T | 233 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(230): Show |
236 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.-462-6440C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382436 | |||||||
| chr22:37382534 | C | T | 234 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(231): Show |
237 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-462-6538G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382534 | |||||||
| chr22:37382552 | TTTTTTTT others(4): Show |
T | 8 | a0001c0001t0009g0306 a0001c0001t0027g0205 a0001c0001t0027g0217 others(5): Show |
8 | HG02145.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-462-6567_-462-655 others(15): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382552 | |||||||
| chr22:37382561 | TTA | T | 9 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0025g0239 others(6): Show |
9 | HG01433.hp2 HG02622.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-462-6567_-462-656 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382561 | |||||||
| chr22:37382562 | T | A | 1 | a0001c0002t0007g0091 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-462-6566A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382562 | |||||||
| chr22:37382562 | TA | T | 203 | a0001c0001t0002g0005 a0001c0001t0002g0043 a0001c0001t0002g0052 others(200): Show |
206 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.-462-6567delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382562 | |||||||
| chr22:37382562 | TAA | T | 15 | a0001c0001t0002g0102 a0001c0001t0003g0008 a0001c0001t0003g0244 others(12): Show |
15 | HG01099.hp1 HG01167.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-462-6568_-462-656 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382562 | |||||||
| chr22:37382563 | A | T | 21 | a0001c0001t0002g0031 a0001c0001t0002g0129 a0001c0001t0002g0241 others(18): Show |
21 | HG00423.hp1 HG00621.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.-462-6567T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382563 | |||||||
| chr22:37382564 | A | T | 224 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(221): Show |
227 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-462-6568T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382564 | |||||||
| chr22:37382612 | C | T | 1 | a0001c0002t0008g0229 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-462-6616G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382612 | |||||||
| chr22:37382616 | C | G | 236 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(233): Show |
239 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.-462-6620G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382616 | |||||||
| chr22:37382772 | G | C | 15 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0025g0239 others(12): Show |
15 | HG01099.hp1 HG01433.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-462-6776C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382772 | |||||||
| chr22:37382782 | G | C | 1 | a0001c0001t0017g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-462-6786C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382782 | |||||||
| chr22:37382924 | C | CT | 3 | a0001c0001t0002g0005 a0001c0001t0002g0279 a0001c0001t0026g0289 |
4 | HG02015.hp1 NA18967.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-6929dupA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382924 | |||||||
| chr22:37382931 | T | C | 15 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0025g0239 others(12): Show |
15 | HG01099.hp1 HG01433.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-462-6935A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382931 | |||||||
| chr22:37382953 | T | C | 2 | a0001c0001t0028g0307 a0001c0003t0070g0167 |
2 | HG02630.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-462-6957A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37382953 | |||||||
| chr22:37383173 | C | T | 1 | a0001c0001t0017g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-462-7177G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383173 | |||||||
| chr22:37383178 | C | A | 1 | a0001c0006t0056g0221 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-462-7182G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383178 | |||||||
| chr22:37383179 | G | A | 237 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(234): Show |
240 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.-462-7183C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383179 | |||||||
| chr22:37383220 | G | A | 1 | a0001c0003t0092g0319 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-462-7224C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383220 | |||||||
| chr22:37383341 | G | A | 239 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(236): Show |
242 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.-462-7345C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383341 | |||||||
| chr22:37383362 | G | A | 3 | a0001c0001t0009g0306 a0001c0001t0064g0305 a0001c0003t0070g0167 |
3 | HG02258.hp2 HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-462-7366C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383362 | |||||||
| chr22:37383445 | T | A | 1 | a0001c0001t0005g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-462-7449A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383445 | |||||||
| chr22:37383673 | G | T | 244 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(241): Show |
247 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.-462-7677C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383673 | |||||||
| chr22:37383681 | G | A | 1 | a0001c0006t0056g0221 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-462-7685C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383681 | |||||||
| chr22:37383789 | C | G | 259 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(256): Show |
262 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.-462-7793G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383789 | |||||||
| chr22:37383911 | G | A | 1 | a0001c0001t0005g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-462-7915C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37383911 | |||||||
| chr22:37384165 | G | A | 2 | a0001c0002t0078g0104 a0001c0003t0001g0017 |
2 | HG00544.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-462-8169C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384165 | |||||||
| chr22:37384184 | G | T | 1 | a0001c0001t0003g0288 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-462-8188C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384184 | |||||||
| chr22:37384482 | G | C | 80 | a0001c0001t0003g0067 a0001c0001t0005g0165 a0001c0001t0005g0210 others(77): Show |
81 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-462-8486C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384482 | |||||||
| chr22:37384522 | T | C | 2 | a0001c0001t0009g0306 a0001c0001t0064g0305 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-462-8526A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384522 | |||||||
| chr22:37384615 | C | A | 80 | a0001c0001t0003g0067 a0001c0001t0005g0165 a0001c0001t0005g0210 others(77): Show |
81 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-462-8619G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384615 | |||||||
| chr22:37384643 | GACCCCTG others(75): Show |
G | 2 | a0001c0003t0001g0061 a0001c0003t0001g0125 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-462-8729_-462-864 others(86): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384643 | |||||||
| chr22:37384651 | GCCTCTCC others(34): Show |
G | 323 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(320): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.-462-8696_-462-865 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384651 | |||||||
| chr22:37384894 | G | A | 1 | a0001c0006t0001g0275 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-462-8898C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37384894 | |||||||
| chr22:37385084 | G | T | 255 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(252): Show |
258 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.-462-9088C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385084 | |||||||
| chr22:37385169 | C | T | 1 | a0001c0001t0065g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-462-9173G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385169 | |||||||
| chr22:37385170 | G | A | 8 | a0001c0001t0005g0210 a0001c0001t0025g0323 a0001c0003t0001g0150 others(5): Show |
8 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-462-9174C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385170 | |||||||
| chr22:37385220 | G | A | 2 | a0001c0001t0009g0306 a0001c0001t0064g0305 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-462-9224C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385220 | |||||||
| chr22:37385313 | G | A | 2 | a0001c0001t0027g0205 a0001c0001t0027g0217 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-9317C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385313 | |||||||
| chr22:37385329 | A | G | 268 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(265): Show |
271 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.-462-9333T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385329 | |||||||
| chr22:37385393 | T | C | 4 | a0001c0001t0025g0323 a0001c0003t0001g0150 a0001c0003t0001g0324 others(1): Show |
4 | HG01884.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-9397A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385393 | |||||||
| chr22:37385502 | C | T | 1 | a0001c0003t0001g0083 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-462-9506G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385502 | |||||||
| chr22:37385551 | G | A | 153 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(150): Show |
155 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.-462-9555C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385551 | |||||||
| chr22:37385733 | G | T | 2 | a0001c0001t0027g0205 a0001c0001t0027g0217 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-462-9737C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385733 | |||||||
| chr22:37385834 | G | T | 262 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(259): Show |
265 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.-462-9838C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37385834 | |||||||
| chr22:37386146 | C | T | 1 | a0001c0001t0003g0283 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-462-10150G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386146 | |||||||
| chr22:37386209 | C | T | 1 | a0001c0003t0006g0121 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-462-10213G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386209 | |||||||
| chr22:37386216 | A | G | 274 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0043 others(271): Show |
277 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.-462-10220T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386216 | |||||||
| chr22:37386522 | C | T | 1 | a0001c0003t0001g0297 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-462-10526G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386522 | |||||||
| chr22:37386527 | G | T | 1 | a0003c0017t0002g0048 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-462-10531C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386527 | |||||||
| chr22:37386703 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-462-10707C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386703 | |||||||
| chr22:37386898 | G | T | 138 | a0001c0001t0002g0043 a0001c0001t0002g0060 a0001c0001t0002g0241 others(135): Show |
138 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-462-10902C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37386898 | |||||||
| chr22:37387033 | C | T | 1 | a0001c0003t0092g0319 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-462-11037G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387033 | |||||||
| chr22:37387106 | T | C | 7 | a0001c0001t0005g0165 a0001c0001t0050g0146 a0001c0002t0069g0142 others(4): Show |
7 | HG01099.hp1 HG02109.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-462-11110A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387106 | |||||||
| chr22:37387230 | C | T | 1 | a0001c0002t0033g0025 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-462-11234G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387230 | |||||||
| chr22:37387311 | G | A | 71 | a0001c0001t0002g0122 a0001c0001t0002g0241 a0001c0001t0002g0248 others(68): Show |
71 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-462-11315C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387311 | |||||||
| chr22:37387363 | T | C | 12 | a0001c0001t0005g0165 a0001c0001t0009g0168 a0001c0001t0009g0169 others(9): Show |
12 | HG02109.hp2 HG02280.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-462-11367A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387363 | |||||||
| chr22:37387636 | G | A | 1 | a0001c0003t0001g0150 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-462-11640C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387636 | |||||||
| chr22:37387650 | G | A | 1 | a0001c0006t0056g0221 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-462-11654C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387650 | |||||||
| chr22:37387693 | C | T | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-11697G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387693 | |||||||
| chr22:37387980 | C | T | 1 | a0001c0003t0041g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-11984G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37387980 | |||||||
| chr22:37388012 | C | G | 1 | a0001c0003t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-462-12016G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388012 | |||||||
| chr22:37388121 | C | T | 12 | a0001c0001t0003g0047 a0001c0001t0003g0179 a0001c0001t0003g0242 others(9): Show |
12 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.-462-12125G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388121 | |||||||
| chr22:37388189 | G | T | 16 | a0001c0001t0003g0047 a0001c0001t0003g0179 a0001c0001t0003g0242 others(13): Show |
16 | HG00099.hp1 HG00597.hp2 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.-462-12193C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388189 | |||||||
| chr22:37388250 | C | T | 1 | a0001c0002t0018g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-462-12254G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388250 | |||||||
| chr22:37388470 | C | G | 13 | a0001c0001t0002g0296 a0001c0001t0003g0047 a0001c0001t0003g0179 others(10): Show |
13 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.-462-12474G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388470 | |||||||
| chr22:37388476 | T | C | 1 | a0001c0003t0006g0121 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-462-12480A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388476 | |||||||
| chr22:37388477 | A | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0070 others(17): Show |
20 | HG01109.hp1 HG01433.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.-462-12481T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388477 | |||||||
| chr22:37388483 | G | A | 5 | a0001c0001t0005g0135 a0001c0001t0005g0136 a0001c0002t0021g0134 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-12487C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388483 | |||||||
| chr22:37388611 | C | T | 4 | a0001c0001t0005g0046 a0001c0001t0005g0165 a0001c0002t0018g0177 others(1): Show |
4 | HG02965.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-12615G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388611 | |||||||
| chr22:37388769 | G | A | 1 | a0001c0003t0041g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-12773C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388769 | |||||||
| chr22:37388970 | A | G | 1 | a0001c0002t0069g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-462-12974T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388970 | |||||||
| chr22:37388996 | T | A | 1 | a0001c0003t0041g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-13000A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37388996 | |||||||
| chr22:37389206 | G | C | 5 | a0001c0002t0008g0229 a0001c0002t0066g0233 a0001c0002t0067g0234 others(2): Show |
5 | HG02818.hp2 HG02895.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-13210C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389206 | |||||||
| chr22:37389378 | C | T | 2 | a0001c0002t0007g0185 a0001c0002t0007g0186 |
2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-462-13382G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389378 | |||||||
| chr22:37389550 | C | T | 1 | a0001c0001t0026g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-462-13554G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389550 | |||||||
| chr22:37389600 | C | T | 11 | a0001c0002t0008g0232 a0001c0002t0008g0312 a0001c0002t0021g0198 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-462-13604G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389600 | |||||||
| chr22:37389729 | C | A | 1 | a0001c0001t0050g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-462-13733G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389729 | |||||||
| chr22:37389760 | T | C | 1 | a0001c0006t0047g0204 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-462-13764A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389760 | |||||||
| chr22:37389836 | G | A | 4 | a0001c0001t0003g0044 a0001c0001t0003g0084 a0001c0001t0003g0086 others(1): Show |
4 | HG00642.hp1 HG01257.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-13840C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389836 | |||||||
| chr22:37389950 | G | C | 1 | a0001c0001t0061g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-462-13954C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389950 | |||||||
| chr22:37389988 | C | T | 3 | a0001c0010t0016g0284 a0001c0010t0016g0291 a0001c0010t0016g0292 |
3 | HG01891.hp1 HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-462-13992G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37389988 | |||||||
| chr22:37390049 | T | A | 6 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0005t0011g0197 others(3): Show |
6 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-462-14053A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390049 | |||||||
| chr22:37390175 | G | C | 11 | a0001c0002t0008g0232 a0001c0002t0008g0312 a0001c0002t0021g0198 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-462-14179C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390175 | |||||||
| chr22:37390551 | G | C | 1 | a0001c0003t0041g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-14555C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390551 | |||||||
| chr22:37390667 | C | T | 2 | a0001c0001t0009g0306 a0001c0001t0064g0305 |
2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-462-14671G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390667 | |||||||
| chr22:37390670 | G | C | 153 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(150): Show |
154 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-462-14674C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390670 | |||||||
| chr22:37390805 | A | G | 1 | a0001c0002t0018g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-462-14809T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390805 | |||||||
| chr22:37390938 | G | A | 1 | a0001c0003t0041g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-14942C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37390938 | |||||||
| chr22:37391089 | G | A | 1 | a0001c0001t0003g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-462-15093C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391089 | |||||||
| chr22:37391181 | G | A | 172 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(169): Show |
173 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.-462-15185C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391181 | |||||||
| chr22:37391273 | G | A | 6 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0172 others(3): Show |
6 | HG02109.hp2 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-15277C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391273 | |||||||
| chr22:37391285 | A | G | 175 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(172): Show |
176 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.-462-15289T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391285 | |||||||
| chr22:37391340 | C | T | 1 | a0001c0002t0032g0039 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-462-15344G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391340 | |||||||
| chr22:37391347 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-462-15351C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391347 | |||||||
| chr22:37391739 | C | T | 2 | a0001c0002t0004g0040 a0006c0014t0004g0034 |
2 | NA19068.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-462-15743G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391739 | |||||||
| chr22:37391842 | A | T | 1 | a0003c0017t0002g0048 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-462-15846T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391842 | |||||||
| chr22:37391899 | G | A | 1 | a0001c0002t0004g0174 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-462-15903C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391899 | |||||||
| chr22:37391916 | G | A | 2 | a0001c0001t0005g0046 a0001c0002t0068g0133 |
2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-462-15920C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37391916 | |||||||
| chr22:37392053 | A | G | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-16057T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392053 | |||||||
| chr22:37392135 | C | G | 6 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0046 others(3): Show |
6 | HG01109.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-16139G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392135 | |||||||
| chr22:37392166 | T | A | 13 | a0001c0001t0003g0047 a0001c0001t0003g0179 a0001c0001t0003g0242 others(10): Show |
13 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.-462-16170A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392166 | |||||||
| chr22:37392318 | C | CT | 112 | a0001c0001t0002g0005 a0001c0001t0002g0052 a0001c0001t0002g0111 others(109): Show |
114 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.-462-16323dupA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392318 | |||||||
| chr22:37392318 | C | CTT | 9 | a0001c0001t0005g0135 a0001c0001t0005g0136 a0001c0001t0017g0128 others(6): Show |
9 | HG00140.hp2 HG02572.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-462-16324_-462-16 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392318 | |||||||
| chr22:37392318 | CT | C | 18 | a0001c0001t0002g0105 a0001c0001t0002g0280 a0001c0001t0005g0070 others(15): Show |
18 | HG00140.hp1 HG01109.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-462-16323delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392318 | |||||||
| chr22:37392325 | T | TC | 10 | a0001c0001t0003g0047 a0001c0001t0003g0179 a0001c0001t0003g0242 others(7): Show |
10 | HG00597.hp2 HG00639.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.-462-16330_-462-16 others(7): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392325 | |||||||
| chr22:37392326 | T | C | 1 | a0004c0012t0001g0243 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-462-16330A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392326 | |||||||
| chr22:37392350 | C | T | 9 | a0001c0002t0008g0232 a0001c0002t0008g0312 a0001c0002t0021g0198 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-462-16354G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392350 | |||||||
| chr22:37392410 | C | A | 1 | a0001c0002t0013g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-462-16414G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392410 | |||||||
| chr22:37392466 | C | T | 4 | a0001c0001t0009g0019 a0001c0001t0063g0322 a0001c0002t0022g0157 others(1): Show |
4 | HG01884.hp1 HG02280.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-16470G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392466 | |||||||
| chr22:37392520 | A | G | 3 | a0001c0001t0053g0090 a0001c0003t0001g0109 a0001c0009t0002g0112 |
3 | NA18939.hp1 NA18943.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-462-16524T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392520 | |||||||
| chr22:37392600 | A | G | 140 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(137): Show |
141 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.-462-16604T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392600 | |||||||
| chr22:37392607 | C | T | 12 | a0001c0002t0004g0200 a0001c0002t0008g0232 a0001c0002t0008g0312 others(9): Show |
12 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-462-16611G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392607 | |||||||
| chr22:37392684 | A | T | 5 | a0001c0002t0022g0311 a0001c0008t0015g0161 a0001c0008t0015g0162 others(2): Show |
5 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-16688T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392684 | |||||||
| chr22:37392812 | T | A | 3 | a0001c0001t0025g0323 a0001c0003t0001g0150 a0001c0003t0001g0324 |
3 | HG02559.hp2 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-462-16816A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392812 | |||||||
| chr22:37392875 | G | A | 1 | a0002c0007t0086g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-462-16879C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392875 | |||||||
| chr22:37392902 | C | A | 1 | a0006c0014t0004g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-462-16906G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392902 | |||||||
| chr22:37392913 | T | A | 1 | a0001c0002t0014g0033 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-462-16917A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37392913 | |||||||
| chr22:37393066 | G | A | 155 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(152): Show |
156 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.-462-17070C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393066 | |||||||
| chr22:37393246 | C | T | 1 | a0001c0001t0003g0288 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-462-17250G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393246 | |||||||
| chr22:37393267 | G | A | 4 | a0001c0001t0009g0019 a0001c0001t0063g0322 a0001c0002t0022g0157 others(1): Show |
4 | HG01884.hp1 HG02280.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-17271C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393267 | |||||||
| chr22:37393281 | G | C | 1 | a0001c0003t0041g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-462-17285C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393281 | |||||||
| chr22:37393422 | C | T | 1 | a0001c0006t0001g0275 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-462-17426G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393422 | |||||||
| chr22:37393502 | G | A | 107 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(104): Show |
108 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-462-17506C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393502 | |||||||
| chr22:37393589 | G | A | 1 | a0001c0002t0089g0131 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-462-17593C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393589 | |||||||
| chr22:37393672 | G | C | 3 | a0001c0003t0042g0230 a0001c0003t0043g0231 a0001c0003t0044g0326 |
3 | NA18906.hp1 NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-462-17676C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393672 | |||||||
| chr22:37393676 | T | C | 19 | a0001c0001t0005g0135 a0001c0001t0005g0136 a0001c0001t0017g0128 others(16): Show |
19 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-462-17680A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393676 | |||||||
| chr22:37393739 | C | T | 4 | a0001c0001t0097g0321 a0001c0002t0008g0312 a0001c0002t0018g0177 others(1): Show |
4 | HG02559.hp1 HG03540.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-462-17743G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393739 | |||||||
| chr22:37393740 | G | A | 2 | a0001c0003t0001g0118 a0002c0007t0086g0313 |
2 | HG01433.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-462-17744C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393740 | |||||||
| chr22:37393778 | G | A | 5 | a0001c0001t0005g0046 a0001c0001t0097g0321 a0001c0002t0018g0177 others(2): Show |
5 | HG02965.hp1 HG03471.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-17782C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393778 | |||||||
| chr22:37393888 | C | T | 2 | a0001c0002t0031g0175 a0001c0002t0031g0176 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-462-17892G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37393888 | |||||||
| chr22:37394060 | C | T | 75 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(72): Show |
76 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-462-18064G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394060 | |||||||
| chr22:37394071 | A | C | 153 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(150): Show |
154 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.-462-18075T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394071 | |||||||
| chr22:37394164 | G | A | 6 | a0001c0002t0008g0229 a0001c0002t0066g0233 a0001c0003t0042g0230 others(3): Show |
6 | HG02895.hp1 HG03098.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-18168C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394164 | |||||||
| chr22:37394175 | C | A | 7 | a0001c0001t0003g0218 a0001c0001t0017g0209 a0001c0001t0017g0316 others(4): Show |
7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-18179G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394175 | |||||||
| chr22:37394228 | C | T | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-18232G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394228 | |||||||
| chr22:37394245 | C | T | 1 | a0001c0001t0025g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-462-18249G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394245 | |||||||
| chr22:37394254 | C | A | 101 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(98): Show |
102 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-462-18258G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394254 | |||||||
| chr22:37394337 | G | A | 7 | a0001c0001t0003g0218 a0001c0001t0017g0209 a0001c0001t0017g0316 others(4): Show |
7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-18341C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394337 | |||||||
| chr22:37394377 | A | G | 1 | a0001c0005t0011g0208 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-462-18381T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394377 | |||||||
| chr22:37394378 | T | C | 6 | a0001c0001t0005g0135 a0001c0001t0005g0136 a0001c0001t0017g0128 others(3): Show |
6 | HG02572.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-462-18382A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394378 | |||||||
| chr22:37394463 | G | A | 82 | a0001c0001t0002g0005 a0001c0001t0002g0052 a0001c0001t0002g0111 others(79): Show |
84 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-462-18467C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394463 | |||||||
| chr22:37394540 | C | G | 1 | a0001c0001t0009g0172 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-462-18544G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394540 | |||||||
| chr22:37394562 | C | T | 7 | a0001c0002t0004g0251 a0001c0002t0006g0247 a0001c0002t0006g0250 others(4): Show |
7 | HG01168.hp2 HG01169.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-18566G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394562 | |||||||
| chr22:37394592 | G | A | 8 | a0001c0001t0003g0218 a0001c0001t0017g0209 a0001c0001t0017g0316 others(5): Show |
8 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-462-18596C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394592 | |||||||
| chr22:37394624 | C | T | 4 | a0001c0001t0009g0019 a0001c0001t0063g0322 a0001c0002t0022g0157 others(1): Show |
4 | HG01884.hp1 HG02280.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-18628G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394624 | |||||||
| chr22:37394649 | C | T | 17 | a0001c0001t0097g0321 a0001c0002t0004g0200 a0001c0002t0008g0232 others(14): Show |
17 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-462-18653G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394649 | |||||||
| chr22:37394778 | A | G | 5 | a0001c0002t0008g0229 a0001c0002t0066g0233 a0001c0003t0042g0230 others(2): Show |
5 | HG02895.hp1 HG03471.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-18782T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394778 | |||||||
| chr22:37394789 | CCGACCTT others(66): Show |
C | 1 | a0006c0014t0004g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-462-18866_-462-18 others(79): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394789 | |||||||
| chr22:37394920 | T | A | 1 | a0001c0003t0083g0220 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-462-18924A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394920 | |||||||
| chr22:37394923 | C | T | 112 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(109): Show |
113 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.-462-18927G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394923 | |||||||
| chr22:37394933 | T | C | 13 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0228 others(10): Show |
13 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-462-18937A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394933 | |||||||
| chr22:37394957 | G | T | 1 | a0001c0002t0008g0232 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-462-18961C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37394957 | |||||||
| chr22:37395029 | C | T | 4 | a0001c0001t0002g0277 a0001c0001t0023g0120 a0001c0002t0004g0040 others(1): Show |
4 | NA18960.hp1 NA18966.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.-462-19033G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395029 | |||||||
| chr22:37395048 | T | C | 7 | a0001c0001t0003g0218 a0001c0001t0017g0209 a0001c0001t0017g0316 others(4): Show |
7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-19052A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395048 | |||||||
| chr22:37395106 | A | AAAAT | 102 | a0001c0001t0002g0005 a0001c0001t0002g0052 a0001c0001t0002g0111 others(99): Show |
104 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.-462-19114_-462-19 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | |||||||
| chr22:37395106 | A | AAAATAAA others(1): Show |
10 | a0001c0002t0004g0238 a0001c0002t0004g0259 a0001c0002t0006g0250 others(7): Show |
10 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.-462-19118_-462-19 others(14): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | |||||||
| chr22:37395106 | AAAAT | A | 22 | a0001c0001t0002g0119 a0001c0001t0003g0140 a0001c0001t0005g0149 others(19): Show |
22 | HG00438.hp2 HG01109.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-462-19114_-462-19 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | |||||||
| chr22:37395106 | AAAATAAA others(1): Show |
A | 87 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(84): Show |
88 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-462-19118_-462-19 others(14): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | |||||||
| chr22:37395106 | AAAATAAA others(5): Show |
A | 23 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0135 others(20): Show |
23 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.-462-19122_-462-19 others(18): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | |||||||
| chr22:37395106 | AAAATAAA others(13): Show |
A | 1 | a0001c0001t0017g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-462-19130_-462-19 others(26): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395106 | |||||||
| chr22:37395130 | TA | T | 7 | a0001c0001t0003g0218 a0001c0001t0017g0209 a0001c0001t0017g0316 others(4): Show |
7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-19135delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395130 | |||||||
| chr22:37395140 | A | C | 1 | a0001c0002t0068g0133 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-462-19144T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395140 | |||||||
| chr22:37395145 | A | G | 15 | a0001c0001t0005g0070 a0001c0001t0005g0149 a0001c0001t0005g0151 others(12): Show |
15 | HG01109.hp1 HG01433.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-462-19149T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395145 | |||||||
| chr22:37395150 | T | G | 42 | a0001c0001t0003g0218 a0001c0001t0005g0020 a0001c0001t0005g0021 others(39): Show |
42 | HG01109.hp2 HG01496.hp1 HG01516.hp1 others(39): Show |
intron_variant | MODIFIER | c.-462-19154A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395150 | |||||||
| chr22:37395270 | T | C | 1 | a0001c0002t0004g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-462-19274A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395270 | |||||||
| chr22:37395422 | G | C | 13 | a0001c0002t0004g0200 a0001c0002t0008g0232 a0001c0002t0008g0312 others(10): Show |
13 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-462-19426C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395422 | |||||||
| chr22:37395482 | T | C | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-19486A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395482 | |||||||
| chr22:37395545 | C | G | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-19549G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395545 | |||||||
| chr22:37395613 | C | T | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-19617G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395613 | |||||||
| chr22:37395718 | G | A | 1 | a0001c0002t0008g0051 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-462-19722C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395718 | |||||||
| chr22:37395752 | G | A | 7 | a0001c0001t0003g0218 a0001c0001t0017g0209 a0001c0001t0017g0316 others(4): Show |
7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-19756C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395752 | |||||||
| chr22:37395798 | G | A | 1 | a0002c0007t0086g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-462-19802C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395798 | |||||||
| chr22:37395806 | C | T | 7 | a0001c0001t0003g0218 a0001c0001t0017g0209 a0001c0001t0017g0316 others(4): Show |
7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-19810G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395806 | |||||||
| chr22:37395856 | G | A | 10 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0172 others(7): Show |
10 | HG02109.hp2 HG02602.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-462-19860C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395856 | |||||||
| chr22:37395941 | C | T | 1 | a0001c0001t0097g0321 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-462-19945G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37395941 | |||||||
| chr22:37396076 | C | T | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-462-20080G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396076 | |||||||
| chr22:37396267 | G | A | 7 | a0001c0001t0003g0218 a0001c0001t0017g0209 a0001c0001t0017g0316 others(4): Show |
7 | HG01496.hp1 HG01516.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-462-20271C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396267 | |||||||
| chr22:37396351 | C | T | 13 | a0001c0001t0005g0165 a0001c0002t0004g0200 a0001c0002t0008g0232 others(10): Show |
13 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-462-20355G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396351 | |||||||
| chr22:37396373 | G | A | 32 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0135 others(29): Show |
32 | HG01109.hp2 HG01891.hp1 HG02145.hp1 others(29): Show |
intron_variant | MODIFIER | c.-462-20377C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396373 | |||||||
| chr22:37396411 | C | A | 1 | a0001c0001t0002g0248 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-462-20415G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396411 | |||||||
| chr22:37396418 | C | T | 1 | a0001c0002t0008g0312 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-462-20422G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396418 | |||||||
| chr22:37396454 | G | A | 5 | a0001c0002t0008g0229 a0001c0002t0066g0233 a0001c0003t0042g0230 others(2): Show |
5 | HG02895.hp1 HG03471.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-20458C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396454 | |||||||
| chr22:37396473 | C | T | 84 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(81): Show |
85 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-462-20477G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396473 | |||||||
| chr22:37396537 | C | T | 85 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(82): Show |
86 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-462-20541G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396537 | |||||||
| chr22:37396550 | A | G | 85 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(82): Show |
86 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-462-20554T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396550 | |||||||
| chr22:37396599 | G | A | 85 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(82): Show |
86 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-462-20603C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396599 | |||||||
| chr22:37396621 | G | A | 1 | a0003c0017t0002g0048 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-462-20625C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396621 | |||||||
| chr22:37396634 | C | T | 1 | a0001c0001t0025g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-462-20638G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396634 | |||||||
| chr22:37396635 | G | A | 5 | a0001c0002t0008g0229 a0001c0002t0066g0233 a0001c0003t0042g0230 others(2): Show |
5 | HG02895.hp1 HG03471.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-462-20639C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396635 | |||||||
| chr22:37396779 | G | A | 1 | a0002c0007t0086g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-462-20783C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396779 | |||||||
| chr22:37396887 | G | A | 2 | a0001c0001t0005g0046 a0001c0002t0068g0133 |
2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-463+20882C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396887 | |||||||
| chr22:37396947 | T | G | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+20822A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396947 | |||||||
| chr22:37396968 | C | T | 1 | a0001c0002t0006g0276 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-463+20801G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396968 | |||||||
| chr22:37396969 | G | C | 1 | a0002c0007t0072g0320 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-463+20800C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37396969 | |||||||
| chr22:37397040 | C | G | 88 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(85): Show |
89 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.-463+20729G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397040 | |||||||
| chr22:37397109 | G | T | 3 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0025g0239 |
3 | HG01433.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-463+20660C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397109 | |||||||
| chr22:37397126 | C | T | 90 | a0001c0001t0002g0005 a0001c0001t0002g0052 a0001c0001t0002g0123 others(87): Show |
91 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.-463+20643G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397126 | |||||||
| chr22:37397156 | A | C | 4 | a0001c0008t0015g0161 a0001c0008t0015g0162 a0001c0008t0015g0171 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+20613T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397156 | |||||||
| chr22:37397240 | C | T | 82 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(79): Show |
83 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-463+20529G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397240 | |||||||
| chr22:37397289 | T | C | 155 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(152): Show |
156 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-463+20480A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397289 | |||||||
| chr22:37397290 | G | A | 79 | a0001c0001t0002g0031 a0001c0001t0002g0101 a0001c0001t0002g0102 others(76): Show |
80 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.-463+20479C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397290 | |||||||
| chr22:37397368 | A | G | 41 | a0001c0001t0002g0270 a0001c0001t0003g0004 a0001c0001t0003g0182 others(38): Show |
42 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-463+20401T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397368 | |||||||
| chr22:37397475 | C | T | 45 | a0001c0001t0002g0296 a0001c0001t0003g0004 a0001c0001t0003g0182 others(42): Show |
46 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.-463+20294G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397475 | |||||||
| chr22:37397476 | G | A | 1 | a0001c0001t0017g0316 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-463+20293C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397476 | |||||||
| chr22:37397510 | A | T | 55 | a0001c0001t0003g0004 a0001c0001t0003g0182 a0001c0001t0003g0189 others(52): Show |
56 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-463+20259T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397510 | |||||||
| chr22:37397613 | T | G | 115 | a0001c0001t0002g0296 a0001c0001t0002g0301 a0001c0001t0003g0004 others(112): Show |
116 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-463+20156A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397613 | |||||||
| chr22:37397695 | C | A | 7 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(4): Show |
7 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+20074G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397695 | |||||||
| chr22:37397710 | C | T | 1 | a0001c0002t0008g0232 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-463+20059G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397710 | |||||||
| chr22:37397787 | GGA | G | 36 | a0001c0001t0003g0004 a0001c0001t0003g0182 a0001c0001t0003g0189 others(33): Show |
37 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-463+19980_-463+19 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397787 | |||||||
| chr22:37397799 | G | GT | 3 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0002c0007t0086g0313 |
3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-463+19969_-463+19 others(7): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397799 | |||||||
| chr22:37397800 | C | T | 3 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0002c0007t0086g0313 |
3 | HG02895.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-463+19969G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397800 | |||||||
| chr22:37397803 | CCGGGCTG others(21): Show |
C | 1 | a0001c0001t0027g0205 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-463+19938_-463+19 others(34): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397803 | |||||||
| chr22:37397805 | G | A | 1 | a0001c0011t0059g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-463+19964C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397805 | |||||||
| chr22:37397841 | G | A | 1 | a0001c0001t0005g0155 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-463+19928C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397841 | |||||||
| chr22:37397882 | T | C | 7 | a0001c0001t0003g0225 a0001c0001t0005g0020 a0001c0001t0005g0021 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-463+19887A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397882 | |||||||
| chr22:37397907 | C | CCT | 7 | a0001c0001t0003g0225 a0001c0001t0005g0020 a0001c0001t0005g0021 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-463+19860_-463+19 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37397907 | |||||||
| chr22:37398014 | G | A | 7 | a0001c0001t0003g0225 a0001c0001t0005g0020 a0001c0001t0005g0021 others(4): Show |
7 | HG02486.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-463+19755C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398014 | |||||||
| chr22:37398025 | A | G | 8 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+19744T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398025 | |||||||
| chr22:37398028 | C | G | 6 | a0001c0001t0003g0179 a0001c0001t0003g0242 a0001c0001t0003g0244 others(3): Show |
6 | HG00140.hp1 HG00733.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-463+19741G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398028 | |||||||
| chr22:37398056 | C | T | 11 | a0001c0001t0003g0225 a0001c0001t0005g0020 a0001c0001t0005g0021 others(8): Show |
11 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+19713G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398056 | |||||||
| chr22:37398059 | T | A | 4 | a0001c0008t0015g0161 a0001c0008t0015g0162 a0001c0008t0015g0171 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+19710A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398059 | |||||||
| chr22:37398062 | G | A | 11 | a0001c0001t0003g0225 a0001c0001t0005g0020 a0001c0001t0005g0021 others(8): Show |
11 | HG02145.hp2 HG02486.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+19707C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398062 | |||||||
| chr22:37398190 | G | A | 1 | a0001c0002t0006g0262 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-463+19579C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398190 | |||||||
| chr22:37398229 | T | C | 182 | a0001c0001t0002g0005 a0001c0001t0002g0052 a0001c0001t0002g0111 others(179): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.-463+19540A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398229 | |||||||
| chr22:37398253 | A | C | 26 | a0001c0001t0003g0218 a0001c0001t0003g0225 a0001c0001t0005g0020 others(23): Show |
26 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.-463+19516T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398253 | |||||||
| chr22:37398259 | T | G | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+19510A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398259 | |||||||
| chr22:37398299 | A | ACGGCCTC others(4): Show |
1 | a0006c0014t0004g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+19469_-463+19 others(17): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398299 | |||||||
| chr22:37398300 | T | A | 1 | a0006c0014t0004g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+19469A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398300 | |||||||
| chr22:37398300 | T | C | 2 | a0001c0002t0008g0232 a0001c0003t0041g0164 |
2 | HG01109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-463+19469A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398300 | |||||||
| chr22:37398319 | C | G | 26 | a0001c0001t0003g0218 a0001c0001t0003g0225 a0001c0001t0005g0020 others(23): Show |
26 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.-463+19450G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398319 | |||||||
| chr22:37398335 | C | A | 1 | a0001c0002t0007g0071 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-463+19434G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398335 | |||||||
| chr22:37398443 | G | A | 33 | a0001c0001t0003g0218 a0001c0001t0003g0225 a0001c0001t0005g0020 others(30): Show |
33 | HG00639.hp2 HG01516.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-463+19326C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398443 | |||||||
| chr22:37398473 | G | A | 1 | a0001c0005t0011g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-463+19296C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398473 | |||||||
| chr22:37398563 | G | A | 24 | a0001c0001t0003g0218 a0001c0001t0003g0225 a0001c0001t0009g0228 others(21): Show |
24 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-463+19206C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398563 | |||||||
| chr22:37398582 | C | T | 24 | a0001c0001t0003g0218 a0001c0001t0003g0225 a0001c0001t0009g0228 others(21): Show |
24 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-463+19187G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398582 | |||||||
| chr22:37398583 | G | A | 1 | a0001c0003t0001g0026 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-463+19186C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398583 | |||||||
| chr22:37398635 | T | A | 19 | a0001c0001t0003g0218 a0001c0001t0009g0228 a0001c0001t0017g0316 others(16): Show |
19 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-463+19134A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398635 | |||||||
| chr22:37398636 | C | T | 19 | a0001c0001t0003g0218 a0001c0001t0009g0228 a0001c0001t0017g0316 others(16): Show |
19 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-463+19133G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398636 | |||||||
| chr22:37398664 | G | A | 1 | a0001c0003t0001g0017 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-463+19105C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398664 | |||||||
| chr22:37398668 | T | G | 5 | a0001c0001t0003g0225 a0001c0002t0074g0224 a0001c0003t0093g0315 others(2): Show |
5 | HG02486.hp2 HG03098.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+19101A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398668 | |||||||
| chr22:37398742 | C | T | 1 | a0001c0001t0005g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-463+19027G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398742 | |||||||
| chr22:37398764 | CAT | C | 5 | a0001c0001t0003g0225 a0001c0002t0074g0224 a0001c0003t0093g0315 others(2): Show |
5 | HG02486.hp2 HG03098.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+19003_-463+19 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398764 | |||||||
| chr22:37398800 | C | T | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+18969G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398800 | |||||||
| chr22:37398811 | G | A | 56 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(53): Show |
57 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.-463+18958C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398811 | |||||||
| chr22:37398814 | C | T | 7 | a0001c0001t0003g0225 a0001c0002t0018g0177 a0001c0002t0069g0142 others(4): Show |
7 | HG01099.hp1 HG02486.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-463+18955G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398814 | |||||||
| chr22:37398893 | C | A | 1 | a0001c0005t0011g0197 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-463+18876G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398893 | |||||||
| chr22:37398990 | A | G | 2 | a0001c0001t0097g0321 a0001c0002t0021g0148 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+18779T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37398990 | |||||||
| chr22:37399063 | T | C | 2 | a0001c0003t0001g0032 a0001c0003t0001g0068 |
2 | HG02074.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-463+18706A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399063 | |||||||
| chr22:37399078 | A | T | 1 | a0001c0009t0055g0015 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-463+18691T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399078 | |||||||
| chr22:37399109 | A | G | 3 | a0001c0001t0029g0096 a0001c0001t0029g0114 a0001c0001t0051g0027 |
3 | HG00621.hp2 HG02056.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-463+18660T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399109 | |||||||
| chr22:37399118 | T | C | 18 | a0001c0001t0003g0218 a0001c0001t0009g0228 a0001c0001t0017g0316 others(15): Show |
18 | HG01516.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-463+18651A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399118 | |||||||
| chr22:37399119 | G | C | 1 | a0001c0003t0083g0220 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-463+18650C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399119 | |||||||
| chr22:37399132 | C | G | 118 | a0001c0001t0002g0005 a0001c0001t0002g0052 a0001c0001t0002g0111 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-463+18637G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399132 | |||||||
| chr22:37399189 | G | A | 118 | a0001c0001t0002g0005 a0001c0001t0002g0052 a0001c0001t0002g0111 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-463+18580C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399189 | |||||||
| chr22:37399221 | C | G | 2 | a0001c0002t0018g0177 a0001c0002t0069g0142 |
2 | HG01099.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-463+18548G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399221 | |||||||
| chr22:37399243 | A | G | 139 | a0001c0001t0002g0005 a0001c0001t0002g0052 a0001c0001t0002g0111 others(136): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-463+18526T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399243 | |||||||
| chr22:37399253 | G | C | 1 | a0006c0014t0004g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+18516C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399253 | |||||||
| chr22:37399472 | A | AGACCACC others(32): Show |
1 | a0001c0002t0007g0071 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-463+18258_-463+18 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399472 | |||||||
| chr22:37399472 | A | AGACCACC others(71): Show |
1 | a0001c0001t0002g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-463+18219_-463+18 others(84): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399472 | |||||||
| chr22:37399472 | A | AGACCACC others(110): Show |
3 | a0001c0001t0005g0154 a0001c0001t0005g0155 a0001c0002t0077g0160 |
3 | HG02896.hp1 HG02970.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-463+18296_-463+18 others(123): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399472 | |||||||
| chr22:37399472 | A | AGACCACC others(149): Show |
3 | a0001c0001t0005g0151 a0001c0001t0005g0152 a0001c0001t0005g0156 |
3 | HG02965.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-463+18296_-463+18 others(162): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399472 | |||||||
| chr22:37399472 | AGACCACC others(71): Show |
A | 23 | a0001c0001t0003g0218 a0001c0001t0009g0228 a0001c0001t0017g0316 others(20): Show |
23 | HG01516.hp1 HG01891.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.-463+18219_-463+18 others(84): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399472 | |||||||
| chr22:37399480 | G | GGCCCACC others(32): Show |
31 | a0001c0001t0005g0046 a0001c0001t0005g0149 a0001c0001t0005g0203 others(28): Show |
31 | HG00423.hp2 HG00639.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-463+18250_-463+18 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399480 | |||||||
| chr22:37399480 | G | GGCCCACC others(149): Show |
1 | a0001c0003t0001g0263 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-463+18288_-463+18 others(162): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399480 | |||||||
| chr22:37399480 | GGCCCACC others(32): Show |
G | 71 | a0001c0001t0002g0005 a0001c0001t0002g0052 a0001c0001t0002g0111 others(68): Show |
73 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-463+18250_-463+18 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399480 | |||||||
| chr22:37399480 | GGCCCACC others(110): Show |
G | 4 | a0001c0002t0021g0198 a0001c0003t0001g0178 a0001c0003t0001g0201 others(1): Show |
4 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-463+18172_-463+18 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399480 | |||||||
| chr22:37399483 | CCACCTCT others(30): Show |
C | 1 | a0006c0014t0004g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+18249_-463+18 others(43): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399483 | |||||||
| chr22:37399519 | A | G | 3 | a0001c0002t0007g0185 a0001c0002t0007g0186 a0001c0002t0008g0232 |
3 | HG01109.hp2 HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-463+18250T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399519 | |||||||
| chr22:37399519 | AGCCCACC others(32): Show |
A | 11 | a0001c0001t0003g0084 a0001c0001t0003g0225 a0001c0001t0060g0227 others(8): Show |
11 | HG01496.hp1 HG02735.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.-463+18211_-463+18 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399519 | |||||||
| chr22:37399557 | C | T | 6 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+18212G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399557 | |||||||
| chr22:37399558 | G | A | 71 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(68): Show |
72 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-463+18211C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399558 | |||||||
| chr22:37399558 | G | GGCCCACC others(71): Show |
10 | a0001c0001t0005g0149 a0001c0001t0005g0203 a0001c0001t0025g0239 others(7): Show |
10 | HG01109.hp1 HG01433.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-463+18133_-463+18 others(84): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399558 | |||||||
| chr22:37399558 | GGCCCACC others(32): Show |
G | 6 | a0001c0001t0003g0140 a0001c0001t0005g0165 a0001c0003t0001g0055 others(3): Show |
6 | HG01346.hp1 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+18172_-463+18 others(45): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399558 | |||||||
| chr22:37399581 | G | GACCACGG others(266): Show |
1 | a0001c0002t0021g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-463+18187_-463+18 others(279): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399581 | |||||||
| chr22:37399581 | G | GACCACGG others(149): Show |
1 | a0001c0001t0097g0321 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-463+18187_-463+18 others(162): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399581 | |||||||
| chr22:37399659 | G | A | 3 | a0001c0001t0002g0277 a0001c0002t0004g0040 a0006c0014t0004g0034 |
3 | NA18966.hp2 NA19068.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-463+18110C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399659 | |||||||
| chr22:37399664 | C | T | 1 | a0001c0003t0094g0011 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-463+18105G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399664 | |||||||
| chr22:37399673 | T | C | 9 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(6): Show |
9 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-463+18096A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399673 | |||||||
| chr22:37399716 | A | G | 85 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(82): Show |
85 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-463+18053T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399716 | |||||||
| chr22:37399727 | C | T | 4 | a0001c0001t0003g0225 a0001c0002t0074g0224 a0001c0003t0093g0315 others(1): Show |
4 | HG02486.hp2 NA18906.hp2 NA20905.hp2 others(1): Show |
intron_variant | MODIFIER | c.-463+18042G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399727 | |||||||
| chr22:37399744 | G | A | 12 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(9): Show |
12 | HG00639.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-463+18025C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399744 | |||||||
| chr22:37399853 | G | A | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+17916C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399853 | |||||||
| chr22:37399917 | G | A | 2 | a0001c0001t0065g0170 a0001c0018t0045g0173 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-463+17852C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37399917 | |||||||
| chr22:37400094 | A | G | 12 | a0001c0001t0005g0203 a0001c0001t0009g0168 a0001c0001t0009g0169 others(9): Show |
12 | HG01433.hp2 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-463+17675T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400094 | |||||||
| chr22:37400116 | A | G | 8 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0172 others(5): Show |
8 | HG02109.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+17653T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400116 | |||||||
| chr22:37400121 | A | C | 8 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0172 others(5): Show |
8 | HG02109.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+17648T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400121 | |||||||
| chr22:37400238 | C | T | 5 | a0001c0002t0004g0143 a0001c0002t0021g0198 a0001c0003t0001g0178 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+17531G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400238 | |||||||
| chr22:37400357 | T | C | 1 | a0001c0001t0003g0225 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-463+17412A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400357 | |||||||
| chr22:37400370 | C | G | 1 | a0001c0001t0061g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-463+17399G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400370 | |||||||
| chr22:37400371 | C | G | 1 | a0001c0001t0061g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-463+17398G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400371 | |||||||
| chr22:37400443 | G | T | 1 | a0006c0014t0004g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+17326C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400443 | |||||||
| chr22:37400585 | G | A | 2 | a0001c0001t0002g0265 a0001c0006t0001g0275 |
2 | HG00558.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-463+17184C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400585 | |||||||
| chr22:37400695 | C | T | 5 | a0001c0001t0005g0165 a0001c0001t0005g0226 a0001c0002t0008g0229 others(2): Show |
5 | HG03041.hp2 HG03453.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-463+17074G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400695 | |||||||
| chr22:37400774 | G | A | 60 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(57): Show |
60 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-463+16995C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400774 | |||||||
| chr22:37400909 | A | G | 2 | a0001c0002t0007g0185 a0001c0002t0007g0186 |
2 | HG02738.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-463+16860T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400909 | |||||||
| chr22:37400937 | G | C | 61 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(58): Show |
61 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-463+16832C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400937 | |||||||
| chr22:37400992 | G | A | 98 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(95): Show |
100 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.-463+16777C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37400992 | |||||||
| chr22:37401098 | A | G | 158 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(155): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-463+16671T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401098 | |||||||
| chr22:37401121 | C | T | 1 | a0003c0017t0002g0048 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-463+16648G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401121 | |||||||
| chr22:37401188 | G | A | 8 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+16581C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401188 | |||||||
| chr22:37401345 | A | G | 5 | a0001c0001t0003g0225 a0001c0002t0074g0224 a0001c0003t0093g0315 others(2): Show |
5 | HG02486.hp2 HG03098.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+16424T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401345 | |||||||
| chr22:37401422 | TC | T | 93 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(90): Show |
95 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.-463+16346delG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401422 | |||||||
| chr22:37401423 | C | A | 1 | a0006c0014t0004g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+16346G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401423 | |||||||
| chr22:37401424 | A | G | 1 | a0006c0014t0004g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+16345T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401424 | |||||||
| chr22:37401522 | A | G | 8 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+16247T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401522 | |||||||
| chr22:37401529 | A | AGGGAGGA others(17): Show |
1 | a0006c0014t0004g0034 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-463+16216_-463+16 others(30): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401529 | |||||||
| chr22:37401589 | C | A | 1 | a0001c0001t0002g0266 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-463+16180G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401589 | |||||||
| chr22:37401657 | G | T | 150 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(147): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-463+16112C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401657 | |||||||
| chr22:37401674 | C | T | 4 | a0001c0001t0005g0203 a0001c0002t0036g0318 a0001c0002t0082g0317 others(1): Show |
4 | HG02257.hp1 HG02717.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-463+16095G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401674 | |||||||
| chr22:37401687 | G | C | 150 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(147): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-463+16082C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401687 | |||||||
| chr22:37401688 | C | G | 150 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(147): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-463+16081G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401688 | |||||||
| chr22:37401689 | G | A | 5 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(2): Show |
5 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-463+16080C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401689 | |||||||
| chr22:37401702 | G | T | 1 | a0002c0007t0072g0320 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-463+16067C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401702 | |||||||
| chr22:37401713 | G | A | 6 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+16056C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401713 | |||||||
| chr22:37401760 | T | C | 158 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(155): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-463+16009A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401760 | |||||||
| chr22:37401836 | C | T | 4 | a0001c0001t0005g0135 a0001c0001t0005g0136 a0001c0001t0017g0128 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+15933G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401836 | |||||||
| chr22:37401837 | G | A | 6 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+15932C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401837 | |||||||
| chr22:37401883 | C | T | 14 | a0001c0001t0003g0218 a0001c0001t0009g0228 a0001c0001t0017g0316 others(11): Show |
14 | HG01516.hp1 HG02280.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-463+15886G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401883 | |||||||
| chr22:37401931 | C | T | 150 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(147): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-463+15838G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401931 | |||||||
| chr22:37401988 | A | G | 4 | a0001c0008t0015g0161 a0001c0008t0015g0162 a0001c0008t0015g0171 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+15781T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37401988 | |||||||
| chr22:37402127 | G | A | 7 | a0001c0001t0005g0165 a0001c0002t0004g0143 a0001c0002t0021g0198 others(4): Show |
7 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+15642C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402127 | |||||||
| chr22:37402227 | G | A | 10 | a0001c0001t0005g0149 a0001c0001t0005g0151 a0001c0001t0005g0152 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-463+15542C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402227 | |||||||
| chr22:37402330 | C | G | 158 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(155): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-463+15439G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402330 | |||||||
| chr22:37402361 | T | C | 4 | a0001c0001t0005g0226 a0001c0002t0008g0229 a0001c0003t0042g0230 others(1): Show |
4 | HG03041.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+15408A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402361 | |||||||
| chr22:37402543 | C | A | 158 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(155): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-463+15226G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402543 | |||||||
| chr22:37402577 | A | C | 1 | a0001c0003t0012g0303 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-463+15192T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402577 | |||||||
| chr22:37402604 | G | T | 150 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(147): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-463+15165C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402604 | |||||||
| chr22:37402624 | GT | G | 150 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(147): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-463+15144delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402624 | |||||||
| chr22:37402659 | A | G | 8 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+15110T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402659 | |||||||
| chr22:37402676 | G | A | 8 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+15093C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402676 | |||||||
| chr22:37402800 | G | A | 1 | a0001c0001t0099g0328 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-463+14969C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402800 | |||||||
| chr22:37402914 | C | T | 3 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0002t0018g0001 |
4 | HG01167.hp2 HG01169.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+14855G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402914 | |||||||
| chr22:37402915 | G | A | 99 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(96): Show |
101 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-463+14854C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402915 | |||||||
| chr22:37402964 | T | A | 10 | a0001c0001t0005g0149 a0001c0001t0005g0151 a0001c0001t0005g0152 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-463+14805A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402964 | |||||||
| chr22:37402989 | G | A | 2 | a0001c0001t0005g0165 a0001c0003t0041g0164 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-463+14780C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37402989 | |||||||
| chr22:37403021 | T | C | 5 | a0001c0002t0004g0143 a0001c0002t0021g0198 a0001c0003t0001g0178 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+14748A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403021 | |||||||
| chr22:37403061 | G | C | 150 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0129 others(147): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.-463+14708C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403061 | |||||||
| chr22:37403096 | CCAA | C | 4 | a0001c0008t0015g0161 a0001c0008t0015g0162 a0001c0008t0015g0171 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+14670_-463+14 others(9): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403096 | |||||||
| chr22:37403148 | G | T | 160 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-463+14621C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403148 | |||||||
| chr22:37403181 | C | T | 160 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-463+14588G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403181 | |||||||
| chr22:37403258 | G | C | 8 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0172 others(5): Show |
8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-463+14511C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403258 | |||||||
| chr22:37403307 | A | G | 8 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+14462T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403307 | |||||||
| chr22:37403329 | A | G | 160 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-463+14440T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403329 | |||||||
| chr22:37403406 | C | T | 1 | a0001c0003t0020g0035 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-463+14363G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403406 | |||||||
| chr22:37403409 | G | GCGAGGGG others(1): Show |
159 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(156): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.-463+14352_-463+14 others(14): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403409 | |||||||
| chr22:37403467 | G | T | 11 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0172 others(8): Show |
11 | HG02109.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+14302C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403467 | |||||||
| chr22:37403498 | A | G | 160 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-463+14271T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403498 | |||||||
| chr22:37403592 | G | A | 1 | a0001c0001t0028g0274 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-463+14177C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403592 | |||||||
| chr22:37403597 | C | T | 71 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(68): Show |
71 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-463+14172G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403597 | |||||||
| chr22:37403622 | C | T | 3 | a0001c0001t0053g0090 a0001c0003t0001g0109 a0001c0009t0002g0112 |
3 | NA18939.hp1 NA18943.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-463+14147G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403622 | |||||||
| chr22:37403624 | C | T | 79 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0129 others(76): Show |
81 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-463+14145G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403624 | |||||||
| chr22:37403779 | G | A | 1 | a0001c0001t0050g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-463+13990C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403779 | |||||||
| chr22:37403794 | G | A | 4 | a0001c0001t0019g0107 a0001c0001t0019g0108 a0001c0002t0004g0023 others(1): Show |
4 | NA18941.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+13975C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403794 | |||||||
| chr22:37403800 | A | C | 2 | a0001c0002t0037g0110 a0001c0002t0037g0113 |
2 | HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-463+13969T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403800 | |||||||
| chr22:37403813 | C | T | 166 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(163): Show |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-463+13956G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403813 | |||||||
| chr22:37403817 | G | A | 89 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(86): Show |
91 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-463+13952C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403817 | |||||||
| chr22:37403839 | T | C | 6 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+13930A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403839 | |||||||
| chr22:37403844 | G | T | 166 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(163): Show |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-463+13925C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403844 | |||||||
| chr22:37403960 | A | G | 121 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(118): Show |
122 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-463+13809T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37403960 | |||||||
| chr22:37404037 | C | T | 2 | a0001c0001t0097g0321 a0001c0002t0021g0148 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+13732G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404037 | |||||||
| chr22:37404073 | C | A | 2 | a0001c0001t0005g0165 a0001c0003t0041g0164 |
2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-463+13696G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404073 | |||||||
| chr22:37404129 | G | A | 95 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(92): Show |
97 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.-463+13640C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404129 | |||||||
| chr22:37404135 | C | T | 61 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(58): Show |
61 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-463+13634G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404135 | |||||||
| chr22:37404265 | C | T | 1 | a0001c0019t0030g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-463+13504G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404265 | |||||||
| chr22:37404297 | C | T | 4 | a0001c0001t0005g0135 a0001c0001t0005g0136 a0001c0001t0017g0128 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+13472G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404297 | |||||||
| chr22:37404309 | G | A | 1 | a0002c0007t0086g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-463+13460C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404309 | |||||||
| chr22:37404383 | G | A | 4 | a0001c0001t0005g0135 a0001c0001t0005g0136 a0001c0001t0017g0128 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+13386C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404383 | |||||||
| chr22:37404456 | G | T | 96 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(93): Show |
98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.-463+13313C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404456 | |||||||
| chr22:37404534 | T | C | 1 | a0001c0006t0056g0221 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-463+13235A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404534 | |||||||
| chr22:37404538 | G | A | 166 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(163): Show |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-463+13231C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404538 | |||||||
| chr22:37404597 | C | A | 4 | a0001c0008t0015g0161 a0001c0008t0015g0162 a0001c0008t0015g0171 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+13172G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404597 | |||||||
| chr22:37404602 | C | T | 61 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(58): Show |
61 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-463+13167G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404602 | |||||||
| chr22:37404678 | T | G | 2 | a0001c0001t0058g0193 a0001c0003t0081g0183 |
2 | HG00099.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.-463+13091A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404678 | |||||||
| chr22:37404723 | C | T | 6 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+13046G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404723 | |||||||
| chr22:37404783 | T | C | 166 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(163): Show |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-463+12986A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404783 | |||||||
| chr22:37404784 | G | A | 166 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(163): Show |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-463+12985C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37404784 | |||||||
| chr22:37405088 | GCAT | G | 8 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0172 others(5): Show |
8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-463+12678_-463+12 others(9): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405088 | |||||||
| chr22:37405089 | C | CT | 7 | a0001c0001t0002g0301 a0001c0001t0017g0128 a0001c0002t0004g0143 others(4): Show |
7 | HG01109.hp2 HG02071.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+12679_-463+12 others(7): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | |||||||
| chr22:37405089 | C | CTT | 14 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0165 others(11): Show |
14 | HG00639.hp2 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-463+12679_-463+12 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | |||||||
| chr22:37405089 | C | CTTT | 4 | a0001c0001t0002g0240 a0001c0001t0025g0239 a0001c0003t0001g0263 others(1): Show |
4 | HG01433.hp2 HG03490.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+12679_-463+12 others(9): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | |||||||
| chr22:37405089 | C | CTTTT | 79 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(76): Show |
79 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.-463+12679_-463+12 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | |||||||
| chr22:37405089 | C | CTTTTT | 8 | a0001c0001t0002g0005 a0001c0001t0002g0265 a0001c0001t0003g0267 others(5): Show |
8 | HG00408.hp2 HG01106.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+12679_-463+12 others(11): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | |||||||
| chr22:37405089 | CA | C | 10 | a0001c0001t0005g0149 a0001c0001t0005g0151 a0001c0001t0005g0152 others(7): Show |
10 | HG01109.hp1 HG02572.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.-463+12679delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405089 | |||||||
| chr22:37405090 | A | AT | 24 | a0001c0001t0002g0102 a0001c0001t0003g0004 a0001c0001t0003g0067 others(21): Show |
25 | HG00099.hp2 HG00438.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.-463+12678dupA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405090 | |||||||
| chr22:37405090 | A | T | 148 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(145): Show |
150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-463+12679T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405090 | |||||||
| chr22:37405090 | AT | A | 15 | a0001c0001t0002g0052 a0001c0001t0003g0086 a0001c0001t0009g0228 others(12): Show |
15 | HG00423.hp2 HG01255.hp1 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-463+12678delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405090 | |||||||
| chr22:37405118 | G | A | 4 | a0001c0001t0005g0135 a0001c0001t0005g0136 a0001c0001t0017g0128 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+12651C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405118 | |||||||
| chr22:37405129 | C | G | 166 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(163): Show |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.-463+12640G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405129 | |||||||
| chr22:37405201 | T | C | 1 | a0001c0002t0069g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-463+12568A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405201 | |||||||
| chr22:37405362 | G | A | 1 | a0002c0007t0086g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-463+12407C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405362 | |||||||
| chr22:37405510 | A | T | 1 | a0002c0007t0072g0320 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-463+12259T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405510 | |||||||
| chr22:37405519 | A | G | 3 | a0001c0002t0013g0076 a0001c0002t0039g0009 a0001c0002t0040g0010 |
3 | HG02071.hp2 NA18949.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-463+12250T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405519 | |||||||
| chr22:37405538 | C | T | 11 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0172 others(8): Show |
11 | HG02109.hp2 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+12231G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405538 | |||||||
| chr22:37405637 | G | T | 1 | a0001c0010t0016g0284 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-463+12132C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405637 | |||||||
| chr22:37405721 | G | C | 105 | a0001c0001t0002g0005 a0001c0001t0002g0111 a0001c0001t0002g0123 others(102): Show |
107 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.-463+12048C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405721 | |||||||
| chr22:37405781 | A | T | 1 | a0001c0001t0003g0283 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-463+11988T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405781 | |||||||
| chr22:37405837 | T | TG | 11 | a0001c0001t0003g0225 a0001c0001t0005g0165 a0001c0002t0008g0232 others(8): Show |
11 | HG00733.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+11931dupC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405837 | |||||||
| chr22:37405840 | A | G | 59 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(56): Show |
59 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-463+11929T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405840 | |||||||
| chr22:37405992 | C | T | 2 | a0001c0002t0031g0175 a0001c0002t0031g0176 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-463+11777G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37405992 | |||||||
| chr22:37406043 | G | A | 84 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(81): Show |
86 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-463+11726C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406043 | |||||||
| chr22:37406100 | C | A | 1 | a0001c0002t0071g0069 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-463+11669G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406100 | |||||||
| chr22:37406182 | G | C | 1 | a0001c0001t0003g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-463+11587C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406182 | |||||||
| chr22:37406208 | G | A | 1 | a0001c0001t0025g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-463+11561C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406208 | |||||||
| chr22:37406307 | G | A | 88 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(85): Show |
90 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.-463+11462C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406307 | |||||||
| chr22:37406326 | C | T | 3 | a0001c0001t0003g0044 a0001c0001t0003g0084 a0001c0001t0003g0086 |
3 | HG01257.hp1 HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.-463+11443G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406326 | |||||||
| chr22:37406354 | G | A | 10 | a0001c0001t0005g0149 a0001c0001t0005g0151 a0001c0001t0005g0152 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-463+11415C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406354 | |||||||
| chr22:37406450 | A | G | 4 | a0001c0008t0015g0161 a0001c0008t0015g0162 a0001c0008t0015g0171 others(1): Show |
4 | HG02109.hp1 HG02615.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+11319T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406450 | |||||||
| chr22:37406523 | C | T | 1 | a0001c0002t0013g0075 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-463+11246G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406523 | |||||||
| chr22:37406780 | C | A | 2 | a0001c0001t0097g0321 a0001c0002t0021g0148 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+10989G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406780 | |||||||
| chr22:37406856 | C | T | 8 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+10913G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406856 | |||||||
| chr22:37406908 | G | A | 1 | a0001c0001t0097g0321 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-463+10861C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37406908 | |||||||
| chr22:37407122 | C | T | 1 | a0001c0002t0008g0232 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-463+10647G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407122 | |||||||
| chr22:37407123 | T | G | 1 | a0001c0002t0008g0232 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-463+10646A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407123 | |||||||
| chr22:37407124 | T | C | 1 | a0001c0002t0008g0232 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-463+10645A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407124 | |||||||
| chr22:37407184 | T | TC | 63 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(60): Show |
63 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.-463+10584dupG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407184 | |||||||
| chr22:37407225 | C | T | 1 | a0001c0003t0001g0138 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-463+10544G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407225 | |||||||
| chr22:37407313 | G | A | 1 | a0002c0007t0086g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-463+10456C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407313 | |||||||
| chr22:37407389 | C | T | 1 | a0001c0002t0004g0029 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-463+10380G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407389 | |||||||
| chr22:37407435 | A | G | 66 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(63): Show |
66 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.-463+10334T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407435 | |||||||
| chr22:37407474 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-463+10295C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407474 | |||||||
| chr22:37407552 | C | T | 1 | a0001c0002t0004g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-463+10217G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407552 | |||||||
| chr22:37407612 | C | T | 1 | a0001c0002t0018g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-463+10157G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407612 | |||||||
| chr22:37407628 | T | A | 1 | a0001c0002t0022g0314 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-463+10141A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407628 | |||||||
| chr22:37407649 | A | G | 2 | a0001c0001t0005g0046 a0001c0001t0005g0070 |
2 | HG01884.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-463+10120T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407649 | |||||||
| chr22:37407680 | G | A | 47 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(44): Show |
47 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-463+10089C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407680 | |||||||
| chr22:37407733 | TA | T | 11 | a0001c0001t0005g0149 a0001c0001t0005g0151 a0001c0001t0005g0152 others(8): Show |
11 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+10035delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407733 | |||||||
| chr22:37407820 | G | A | 4 | a0001c0001t0025g0323 a0001c0001t0063g0322 a0001c0003t0001g0150 others(1): Show |
4 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-463+9949C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407820 | |||||||
| chr22:37407850 | G | A | 11 | a0001c0001t0005g0149 a0001c0001t0005g0151 a0001c0001t0005g0152 others(8): Show |
11 | HG01109.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+9919C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407850 | |||||||
| chr22:37407850 | G | T | 85 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(82): Show |
87 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-463+9919C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407850 | |||||||
| chr22:37407851 | C | T | 8 | a0001c0001t0005g0165 a0001c0002t0004g0143 a0001c0002t0008g0232 others(5): Show |
8 | HG01109.hp2 HG02145.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+9918G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407851 | |||||||
| chr22:37407910 | G | A | 8 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+9859C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407910 | |||||||
| chr22:37407997 | C | G | 8 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+9772G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37407997 | |||||||
| chr22:37408007 | T | C | 1 | a0001c0001t0005g0210 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-463+9762A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408007 | |||||||
| chr22:37408034 | T | C | 1 | a0001c0003t0094g0011 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-463+9735A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408034 | |||||||
| chr22:37408136 | G | A | 66 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(63): Show |
66 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.-463+9633C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408136 | |||||||
| chr22:37408158 | A | G | 1 | a0001c0002t0004g0249 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-463+9611T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408158 | |||||||
| chr22:37408229 | G | A | 2 | a0001c0001t0003g0007 a0001c0001t0003g0008 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-463+9540C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408229 | |||||||
| chr22:37408283 | C | T | 2 | a0001c0001t0097g0321 a0001c0002t0021g0148 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+9486G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408283 | |||||||
| chr22:37408303 | G | A | 2 | a0001c0001t0003g0140 a0001c0003t0001g0138 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-463+9466C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408303 | |||||||
| chr22:37408412 | G | A | 1 | a0001c0001t0050g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-463+9357C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408412 | |||||||
| chr22:37408682 | G | A | 6 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+9087C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408682 | |||||||
| chr22:37408955 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-463+8814C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37408955 | |||||||
| chr22:37409040 | G | C | 10 | a0001c0001t0005g0165 a0001c0002t0004g0143 a0001c0002t0008g0232 others(7): Show |
10 | HG01109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-463+8729C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409040 | |||||||
| chr22:37409163 | C | T | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+8606G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409163 | |||||||
| chr22:37409223 | C | A | 2 | a0001c0001t0009g0019 a0001c0002t0022g0157 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-463+8546G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409223 | |||||||
| chr22:37409239 | G | A | 6 | a0001c0001t0003g0044 a0001c0001t0003g0084 a0001c0001t0003g0086 others(3): Show |
6 | HG00642.hp1 HG01257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-463+8530C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409239 | |||||||
| chr22:37409250 | G | A | 1 | a0001c0003t0083g0220 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-463+8519C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409250 | |||||||
| chr22:37409385 | G | A | 2 | a0001c0001t0097g0321 a0001c0002t0021g0148 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+8384C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409385 | |||||||
| chr22:37409404 | C | G | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+8365G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409404 | |||||||
| chr22:37409450 | C | T | 3 | a0001c0002t0008g0229 a0001c0003t0042g0230 a0001c0003t0043g0231 |
3 | HG03471.hp1 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-463+8319G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409450 | |||||||
| chr22:37409487 | G | A | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+8282C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409487 | |||||||
| chr22:37409551 | C | T | 1 | a0001c0002t0007g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-463+8218G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409551 | |||||||
| chr22:37409677 | A | G | 71 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(68): Show |
71 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.-463+8092T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409677 | |||||||
| chr22:37409705 | C | T | 1 | a0001c0003t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-463+8064G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409705 | |||||||
| chr22:37409725 | T | G | 47 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(44): Show |
47 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.-463+8044A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409725 | |||||||
| chr22:37409813 | A | T | 1 | a0001c0001t0029g0114 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-463+7956T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409813 | |||||||
| chr22:37409835 | G | A | 76 | a0001c0001t0002g0005 a0001c0001t0002g0129 a0001c0001t0002g0240 others(73): Show |
78 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-463+7934C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37409835 | |||||||
| chr22:37410136 | C | T | 2 | a0001c0002t0037g0110 a0001c0002t0037g0113 |
2 | HG01256.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.-463+7633G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410136 | |||||||
| chr22:37410158 | C | T | 2 | a0001c0001t0097g0321 a0001c0002t0021g0148 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+7611G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410158 | |||||||
| chr22:37410237 | C | T | 28 | a0001c0001t0003g0004 a0001c0001t0003g0182 a0001c0001t0003g0189 others(25): Show |
29 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.-463+7532G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410237 | |||||||
| chr22:37410245 | C | T | 7 | a0001c0002t0004g0143 a0001c0002t0008g0312 a0001c0002t0021g0198 others(4): Show |
7 | HG02145.hp2 HG02559.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+7524G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410245 | |||||||
| chr22:37410308 | G | A | 5 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0005t0011g0197 others(2): Show |
5 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+7461C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410308 | |||||||
| chr22:37410365 | T | C | 1 | a0001c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-463+7404A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410365 | |||||||
| chr22:37410372 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-463+7397C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410372 | |||||||
| chr22:37410422 | G | A | 4 | a0001c0001t0005g0135 a0001c0001t0005g0136 a0001c0001t0017g0128 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+7347C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410422 | |||||||
| chr22:37410448 | G | T | 8 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(5): Show |
8 | HG00639.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-463+7321C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410448 | |||||||
| chr22:37410473 | G | A | 1 | a0001c0004t0010g0302 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-463+7296C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410473 | |||||||
| chr22:37410560 | A | C | 1 | a0001c0002t0004g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-463+7209T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410560 | |||||||
| chr22:37410755 | G | A | 6 | a0001c0001t0003g0225 a0001c0002t0074g0224 a0001c0003t0092g0319 others(3): Show |
6 | HG02486.hp2 HG03098.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+7014C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410755 | |||||||
| chr22:37410831 | A | G | 85 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(82): Show |
85 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.-463+6938T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410831 | |||||||
| chr22:37410880 | A | G | 85 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(82): Show |
85 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.-463+6889T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410880 | |||||||
| chr22:37410923 | G | A | 30 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(27): Show |
30 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.-463+6846C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410923 | |||||||
| chr22:37410970 | C | T | 1 | a0002c0007t0072g0320 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-463+6799G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410970 | |||||||
| chr22:37410974 | A | G | 1 | a0001c0001t0061g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-463+6795T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37410974 | |||||||
| chr22:37411004 | G | A | 1 | a0001c0001t0002g0241 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-463+6765C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411004 | |||||||
| chr22:37411062 | G | A | 85 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(82): Show |
85 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.-463+6707C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411062 | |||||||
| chr22:37411070 | A | G | 85 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(82): Show |
85 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.-463+6699T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411070 | |||||||
| chr22:37411079 | A | G | 5 | a0001c0002t0018g0177 a0001c0002t0021g0198 a0001c0003t0001g0178 others(2): Show |
5 | HG02145.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+6690T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411079 | |||||||
| chr22:37411264 | A | C | 89 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(86): Show |
89 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.-463+6505T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411264 | |||||||
| chr22:37411343 | C | CTT | 9 | a0001c0001t0002g0111 a0001c0001t0019g0107 a0001c0001t0019g0108 others(6): Show |
9 | NA18939.hp1 NA18941.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-463+6425_-463+642 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411343 | |||||||
| chr22:37411344 | A | T | 9 | a0001c0001t0002g0111 a0001c0001t0019g0107 a0001c0001t0019g0108 others(6): Show |
9 | NA18939.hp1 NA18941.hp1 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-463+6425T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411344 | |||||||
| chr22:37411405 | TG | T | 208 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(205): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-463+6363delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411405 | |||||||
| chr22:37411417 | G | C | 5 | a0001c0002t0088g0285 a0001c0003t0012g0290 a0001c0010t0016g0284 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-463+6352C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411417 | |||||||
| chr22:37411469 | G | A | 2 | a0001c0002t0006g0268 a0001c0002t0006g0269 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-463+6300C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411469 | |||||||
| chr22:37411710 | A | C | 5 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(2): Show |
5 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-463+6059T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37411710 | |||||||
| chr22:37412011 | G | A | 11 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(8): Show |
11 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-463+5758C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412011 | |||||||
| chr22:37412082 | G | C | 83 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(80): Show |
83 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-463+5687C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412082 | |||||||
| chr22:37412173 | G | C | 77 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(74): Show |
77 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-463+5596C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412173 | |||||||
| chr22:37412244 | C | G | 1 | a0001c0003t0041g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-463+5525G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412244 | |||||||
| chr22:37412277 | C | CA | 6 | a0001c0001t0005g0070 a0001c0001t0009g0228 a0001c0002t0004g0200 others(3): Show |
7 | HG01884.hp2 HG02886.hp1 NA18975.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+5491dupT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412277 | |||||||
| chr22:37412277 | C | CAAAAA | 20 | a0001c0001t0005g0151 a0001c0001t0005g0226 a0001c0001t0009g0211 others(17): Show |
20 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.-463+5487_-463+549 others(9): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412277 | |||||||
| chr22:37412277 | C | CAAAAAA | 21 | a0001c0001t0005g0020 a0001c0001t0005g0149 a0001c0001t0005g0152 others(18): Show |
21 | HG01109.hp1 HG01109.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-463+5486_-463+549 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412277 | |||||||
| chr22:37412277 | C | CAAAAAAA | 7 | a0001c0001t0005g0021 a0001c0001t0005g0155 a0001c0001t0009g0019 others(4): Show |
7 | HG01884.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-463+5485_-463+549 others(11): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412277 | |||||||
| chr22:37412277 | CA | C | 82 | a0001c0001t0002g0005 a0001c0001t0002g0052 a0001c0001t0002g0123 others(79): Show |
84 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.-463+5491delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412277 | |||||||
| chr22:37412292 | A | AAAAAAG | 25 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0005g0135 others(22): Show |
25 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.-463+5476_-463+547 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412292 | |||||||
| chr22:37412292 | A | G | 4 | a0001c0001t0019g0107 a0001c0001t0019g0108 a0001c0002t0004g0023 others(1): Show |
4 | NA18941.hp1 NA18950.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+5477T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412292 | |||||||
| chr22:37412309 | G | A | 83 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(80): Show |
83 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-463+5460C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412309 | |||||||
| chr22:37412310 | G | GA | 10 | a0001c0001t0002g0126 a0001c0001t0003g0194 a0001c0001t0003g0288 others(7): Show |
10 | HG00735.hp1 HG00735.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.-463+5458dupT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412310 | |||||||
| chr22:37412375 | C | T | 1 | a0001c0006t0048g0132 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-463+5394G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412375 | |||||||
| chr22:37412379 | G | A | 1 | a0001c0001t0002g0241 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-463+5390C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412379 | |||||||
| chr22:37412575 | G | A | 2 | a0001c0002t0004g0293 a0001c0002t0079g0237 |
2 | HG00597.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-463+5194C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412575 | |||||||
| chr22:37412719 | C | T | 1 | a0001c0002t0004g0089 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-463+5050G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412719 | |||||||
| chr22:37412845 | A | G | 83 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(80): Show |
83 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.-463+4924T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412845 | |||||||
| chr22:37412872 | T | C | 168 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(165): Show |
170 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.-463+4897A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412872 | |||||||
| chr22:37412928 | C | T | 1 | a0001c0003t0094g0011 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-463+4841G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412928 | |||||||
| chr22:37412952 | T | C | 70 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(67): Show |
70 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.-463+4817A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412952 | |||||||
| chr22:37412966 | G | C | 1 | a0001c0002t0004g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-463+4803C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37412966 | |||||||
| chr22:37413102 | G | A | 30 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(27): Show |
30 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.-463+4667C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413102 | |||||||
| chr22:37413199 | G | A | 74 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(71): Show |
76 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.-463+4570C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413199 | |||||||
| chr22:37413396 | G | A | 74 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(71): Show |
76 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.-463+4373C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413396 | |||||||
| chr22:37413403 | CAA | C | 59 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(56): Show |
59 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.-463+4364_-463+436 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413403 | |||||||
| chr22:37413439 | G | A | 79 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(76): Show |
81 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-463+4330C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413439 | |||||||
| chr22:37413440 | T | C | 1 | a0001c0006t0001g0275 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-463+4329A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413440 | |||||||
| chr22:37413463 | G | A | 21 | a0001c0001t0005g0210 a0001c0001t0009g0168 a0001c0001t0009g0169 others(18): Show |
21 | HG00639.hp2 HG01891.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-463+4306C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413463 | |||||||
| chr22:37413563 | C | A | 30 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(27): Show |
30 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.-463+4206G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413563 | |||||||
| chr22:37413568 | T | TA | 20 | a0001c0001t0003g0225 a0001c0001t0003g0283 a0001c0001t0005g0149 others(17): Show |
20 | HG01109.hp1 HG02055.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.-463+4200dupT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413568 | |||||||
| chr22:37413568 | TA | T | 22 | a0001c0001t0002g0280 a0001c0001t0002g0294 a0001c0001t0002g0296 others(19): Show |
22 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.-463+4200delT | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413568 | |||||||
| chr22:37413612 | TG | T | 6 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+4156delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413612 | |||||||
| chr22:37413616 | G | A | 66 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(63): Show |
66 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.-463+4153C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413616 | |||||||
| chr22:37413732 | G | A | 101 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(98): Show |
103 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-463+4037C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413732 | |||||||
| chr22:37413783 | T | G | 1 | a0001c0002t0021g0134 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-463+3986A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413783 | |||||||
| chr22:37413814 | G | A | 1 | a0001c0001t0098g0327 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-463+3955C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413814 | |||||||
| chr22:37413877 | G | A | 1 | a0001c0001t0017g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-463+3892C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413877 | |||||||
| chr22:37413915 | G | A | 1 | a0001c0004t0010g0302 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-463+3854C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413915 | |||||||
| chr22:37413960 | G | A | 8 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0172 others(5): Show |
8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-463+3809C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37413960 | |||||||
| chr22:37414004 | G | A | 6 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+3765C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414004 | |||||||
| chr22:37414044 | T | A | 9 | a0001c0001t0005g0165 a0001c0002t0008g0232 a0001c0002t0018g0177 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-463+3725A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414044 | |||||||
| chr22:37414136 | T | C | 58 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(55): Show |
58 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-463+3633A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414136 | |||||||
| chr22:37414257 | T | G | 13 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(10): Show |
13 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-463+3512A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414257 | |||||||
| chr22:37414329 | G | A | 6 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(3): Show |
6 | HG01884.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-463+3440C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414329 | |||||||
| chr22:37414363 | G | A | 2 | a0001c0002t0031g0175 a0001c0002t0031g0176 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-463+3406C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414363 | |||||||
| chr22:37414417 | C | G | 58 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(55): Show |
58 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-463+3352G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414417 | |||||||
| chr22:37414452 | A | T | 58 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(55): Show |
58 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-463+3317T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414452 | |||||||
| chr22:37414575 | C | A | 1 | a0001c0001t0005g0156 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-463+3194G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414575 | |||||||
| chr22:37414653 | G | A | 67 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(64): Show |
67 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(64): Show |
intron_variant | MODIFIER | c.-463+3116C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414653 | |||||||
| chr22:37414668 | C | A | 69 | a0001c0001t0002g0005 a0001c0001t0002g0129 a0001c0001t0002g0240 others(66): Show |
71 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.-463+3101G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414668 | |||||||
| chr22:37414713 | T | C | 1 | a0001c0002t0004g0085 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-463+3056A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414713 | |||||||
| chr22:37414738 | A | G | 80 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(77): Show |
80 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.-463+3031T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414738 | |||||||
| chr22:37414807 | C | G | 9 | a0001c0001t0005g0165 a0001c0002t0008g0232 a0001c0002t0018g0177 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.-463+2962G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414807 | |||||||
| chr22:37414826 | G | A | 13 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(10): Show |
13 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-463+2943C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414826 | |||||||
| chr22:37414990 | G | C | 1 | a0001c0002t0021g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-463+2779C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37414990 | |||||||
| chr22:37415185 | GTCC | G | 66 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(63): Show |
66 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.-463+2581_-463+258 others(7): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415185 | |||||||
| chr22:37415200 | T | G | 171 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(168): Show |
173 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.-463+2569A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415200 | |||||||
| chr22:37415239 | G | T | 2 | a0001c0002t0033g0025 a0001c0003t0001g0026 |
2 | HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-463+2530C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415239 | |||||||
| chr22:37415395 | G | A | 2 | a0001c0001t0097g0321 a0001c0002t0021g0148 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-463+2374C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415395 | |||||||
| chr22:37415595 | C | G | 2 | a0001c0002t0033g0025 a0001c0003t0001g0026 |
2 | HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-463+2174G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415595 | |||||||
| chr22:37415599 | G | A | 2 | a0001c0003t0012g0303 a0001c0003t0034g0006 |
3 | HG03490.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-463+2170C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415599 | |||||||
| chr22:37415737 | T | C | 35 | a0001c0001t0003g0225 a0001c0001t0005g0020 a0001c0001t0005g0021 others(32): Show |
35 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-463+2032A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415737 | |||||||
| chr22:37415790 | A | G | 19 | a0001c0001t0003g0225 a0001c0001t0005g0020 a0001c0001t0005g0021 others(16): Show |
19 | HG01109.hp2 HG01884.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.-463+1979T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415790 | |||||||
| chr22:37415797 | C | T | 5 | a0001c0002t0088g0285 a0001c0003t0012g0290 a0001c0010t0016g0284 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-463+1972G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415797 | |||||||
| chr22:37415806 | C | T | 10 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(7): Show |
10 | HG01884.hp1 HG02622.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.-463+1963G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415806 | |||||||
| chr22:37415833 | G | A | 20 | a0001c0001t0003g0225 a0001c0001t0005g0020 a0001c0001t0005g0021 others(17): Show |
20 | HG01109.hp2 HG01884.hp1 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.-463+1936C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415833 | |||||||
| chr22:37415895 | G | A | 1 | a0001c0002t0006g0276 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-463+1874C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415895 | |||||||
| chr22:37415919 | T | C | 1 | a0002c0007t0072g0320 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-463+1850A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415919 | |||||||
| chr22:37415969 | A | T | 21 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0105 others(18): Show |
21 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.-463+1800T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415969 | |||||||
| chr22:37415986 | A | G | 22 | a0001c0001t0003g0225 a0001c0001t0005g0020 a0001c0001t0005g0021 others(19): Show |
22 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.-463+1783T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37415986 | |||||||
| chr22:37416105 | G | A | 10 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-463+1664C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416105 | |||||||
| chr22:37416127 | C | T | 1 | a0001c0001t0005g0046 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-463+1642G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416127 | |||||||
| chr22:37416131 | G | A | 102 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(99): Show |
104 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.-463+1638C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416131 | |||||||
| chr22:37416240 | G | A | 1 | a0001c0001t0027g0217 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-463+1529C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416240 | |||||||
| chr22:37416341 | C | T | 41 | a0001c0001t0003g0004 a0001c0001t0003g0182 a0001c0001t0003g0189 others(38): Show |
42 | HG00099.hp2 HG00423.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-463+1428G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416341 | |||||||
| chr22:37416359 | T | C | 1 | a0001c0002t0018g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-463+1410A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416359 | |||||||
| chr22:37416456 | C | T | 5 | a0001c0001t0003g0044 a0001c0001t0003g0084 a0001c0001t0003g0086 others(2): Show |
5 | HG01257.hp1 HG02451.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.-463+1313G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416456 | |||||||
| chr22:37416541 | G | A | 3 | a0001c0002t0036g0318 a0001c0002t0082g0317 a0001c0003t0083g0220 |
3 | HG02717.hp2 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-463+1228C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416541 | |||||||
| chr22:37416646 | C | T | 1 | a0001c0002t0069g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-463+1123G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416646 | |||||||
| chr22:37416710 | C | G | 3 | a0001c0002t0021g0134 a0001c0002t0068g0133 a0001c0006t0048g0132 |
3 | HG02572.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-463+1059G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416710 | |||||||
| chr22:37416872 | A | G | 156 | a0001c0001t0002g0031 a0001c0001t0002g0043 a0001c0001t0002g0052 others(153): Show |
159 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.-463+897T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416872 | |||||||
| chr22:37416916 | T | C | 1 | a0001c0002t0069g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-463+853A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416916 | |||||||
| chr22:37416980 | T | C | 259 | a0001c0001t0002g0031 a0001c0001t0002g0043 a0001c0001t0002g0052 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.-463+789A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37416980 | |||||||
| chr22:37417040 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-463+729C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417040 | |||||||
| chr22:37417049 | C | T | 1 | a0002c0007t0086g0313 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-463+720G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417049 | |||||||
| chr22:37417069 | A | G | 1 | a0001c0003t0038g0074 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-463+700T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417069 | |||||||
| chr22:37417122 | GCCTCT | G | 4 | a0001c0001t0005g0226 a0001c0002t0008g0229 a0001c0003t0042g0230 others(1): Show |
4 | HG03041.hp2 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-463+642_-463+646d others(7): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417122 | |||||||
| chr22:37417130 | T | C | 1 | a0001c0003t0094g0011 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-463+639A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417130 | |||||||
| chr22:37417392 | A | T | 8 | a0001c0001t0009g0168 a0001c0001t0009g0169 a0001c0001t0009g0172 others(5): Show |
8 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-463+377T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417392 | |||||||
| chr22:37417448 | G | T | 1 | a0001c0001t0005g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-463+321C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417448 | |||||||
| chr22:37417567 | C | T | 2 | a0001c0002t0008g0312 a0001c0002t0022g0311 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-463+202G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417567 | |||||||
| chr22:37417650 | A | C | 1 | a0001c0001t0002g0248 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-463+119T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417650 | |||||||
| chr22:37417754 | G | A | 1 | a0001c0002t0006g0196 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-463+15C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 2/2 | chr22 | 37417754 | |||||||
| chr22:37418043 | C | T | 1 | a0001c0003t0092g0319 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-613-124G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418043 | |||||||
| chr22:37418119 | G | C | 11 | a0001c0001t0023g0077 a0001c0001t0023g0120 a0001c0002t0013g0075 others(8): Show |
11 | HG02056.hp1 HG02071.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.-613-200C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418119 | |||||||
| chr22:37418316 | T | C | 13 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(10): Show |
13 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-613-397A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418316 | |||||||
| chr22:37418521 | C | T | 1 | a0001c0002t0036g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-613-602G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418521 | |||||||
| chr22:37418524 | G | C | 12 | a0001c0001t0005g0210 a0001c0001t0009g0211 a0001c0001t0017g0209 others(9): Show |
12 | HG00639.hp2 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-613-605C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418524 | |||||||
| chr22:37418668 | C | T | 1 | a0001c0003t0041g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-613-749G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418668 | |||||||
| chr22:37418884 | A | G | 87 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(84): Show |
89 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.-613-965T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418884 | |||||||
| chr22:37418938 | G | A | 4 | a0001c0002t0008g0081 a0001c0002t0008g0093 a0001c0003t0001g0082 others(1): Show |
4 | NA18943.hp2 NA18969.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.-613-1019C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37418938 | |||||||
| chr22:37419000 | A | G | 99 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(96): Show |
101 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.-613-1081T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419000 | |||||||
| chr22:37419069 | G | C | 2 | a0001c0001t0097g0321 a0001c0002t0021g0148 |
2 | HG03540.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-613-1150C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419069 | |||||||
| chr22:37419078 | A | G | 1 | a0001c0015t0080g0223 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-613-1159T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419078 | |||||||
| chr22:37419334 | AAC | A | 10 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-613-1417_-613-141 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419334 | |||||||
| chr22:37419469 | T | C | 1 | a0001c0003t0094g0011 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-613-1550A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419469 | |||||||
| chr22:37419844 | C | G | 2 | a0001c0001t0003g0007 a0001c0001t0003g0008 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-613-1925G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419844 | |||||||
| chr22:37419908 | C | G | 259 | a0001c0001t0002g0031 a0001c0001t0002g0043 a0001c0001t0002g0052 others(256): Show |
263 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.-613-1989G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37419908 | |||||||
| chr22:37420056 | C | A | 5 | a0001c0002t0088g0285 a0001c0003t0012g0290 a0001c0010t0016g0284 others(2): Show |
5 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-613-2137G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420056 | |||||||
| chr22:37420079 | C | A | 1 | a0001c0001t0003g0288 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-613-2160G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420079 | |||||||
| chr22:37420163 | G | C | 1 | a0001c0001t0003g0087 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-613-2244C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420163 | |||||||
| chr22:37420343 | C | G | 1 | a0001c0002t0007g0304 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-613-2424G>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420343 | |||||||
| chr22:37420435 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-613-2516C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420435 | |||||||
| chr22:37420661 | G | C | 1 | a0001c0003t0001g0138 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-613-2742C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420661 | |||||||
| chr22:37420708 | AG | A | 89 | a0001c0001t0002g0005 a0001c0001t0002g0129 a0001c0001t0002g0240 others(86): Show |
91 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-613-2790delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420708 | |||||||
| chr22:37420794 | A | G | 12 | a0001c0001t0003g0225 a0001c0001t0017g0316 a0001c0001t0097g0321 others(9): Show |
12 | HG01516.hp1 HG02486.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-613-2875T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420794 | |||||||
| chr22:37420824 | T | A | 11 | a0001c0001t0003g0225 a0001c0001t0017g0316 a0001c0001t0097g0321 others(8): Show |
11 | HG01516.hp1 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-613-2905A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420824 | |||||||
| chr22:37420899 | G | A | 68 | a0001c0001t0002g0005 a0001c0001t0002g0129 a0001c0001t0002g0240 others(65): Show |
70 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.-613-2980C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420899 | |||||||
| chr22:37420938 | T | C | 1 | a0001c0009t0055g0015 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-613-3019A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420938 | |||||||
| chr22:37420959 | A | G | 1 | a0001c0001t0003g0207 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-613-3040T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37420959 | |||||||
| chr22:37421008 | G | C | 13 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(10): Show |
13 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(10): Show |
intron_variant | MODIFIER | c.-613-3089C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421008 | |||||||
| chr22:37421633 | G | A | 14 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.-613-3714C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421633 | |||||||
| chr22:37421686 | G | A | 1 | a0001c0001t0025g0239 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-613-3767C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421686 | |||||||
| chr22:37421756 | G | A | 2 | a0001c0001t0002g0122 a0001c0003t0006g0121 |
2 | HG00741.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.-613-3837C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421756 | |||||||
| chr22:37421782 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-613-3863G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421782 | |||||||
| chr22:37421823 | G | A | 7 | a0001c0001t0005g0135 a0001c0001t0005g0136 a0001c0001t0005g0203 others(4): Show |
7 | HG02055.hp2 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.-613-3904C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421823 | |||||||
| chr22:37421848 | C | A | 9 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-613-3929G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421848 | |||||||
| chr22:37421973 | G | T | 11 | a0001c0001t0003g0225 a0001c0001t0017g0316 a0001c0001t0097g0321 others(8): Show |
11 | HG01516.hp1 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-613-4054C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37421973 | |||||||
| chr22:37422067 | A | G | 1 | a0001c0003t0001g0094 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-613-4148T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422067 | |||||||
| chr22:37422073 | C | T | 207 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(204): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-613-4154G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422073 | |||||||
| chr22:37422201 | G | C | 78 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(75): Show |
80 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-613-4282C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422201 | |||||||
| chr22:37422292 | G | T | 76 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(73): Show |
78 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-613-4373C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422292 | |||||||
| chr22:37422340 | T | C | 1 | a0001c0003t0001g0042 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-613-4421A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422340 | |||||||
| chr22:37422379 | C | T | 90 | a0001c0001t0002g0005 a0001c0001t0002g0129 a0001c0001t0002g0240 others(87): Show |
92 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.-613-4460G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422379 | |||||||
| chr22:37422380 | GT | G | 23 | a0001c0001t0003g0225 a0001c0001t0005g0020 a0001c0001t0005g0021 others(20): Show |
23 | HG01109.hp2 HG01516.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.-613-4462delA | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422380 | |||||||
| chr22:37422435 | A | G | 97 | a0001c0001t0002g0005 a0001c0001t0002g0123 a0001c0001t0002g0129 others(94): Show |
99 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.-613-4516T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422435 | |||||||
| chr22:37422469 | G | A | 1 | a0001c0002t0004g0085 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-613-4550C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422469 | |||||||
| chr22:37422596 | T | C | 1 | a0001c0003t0041g0164 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-613-4677A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422596 | |||||||
| chr22:37422887 | G | A | 9 | a0001c0001t0017g0316 a0001c0002t0008g0312 a0001c0002t0022g0311 others(6): Show |
9 | HG01516.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+4411C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422887 | |||||||
| chr22:37422943 | C | CG | 44 | a0001c0001t0002g0031 a0001c0001t0003g0182 a0001c0001t0003g0218 others(41): Show |
44 | HG00423.hp2 HG00733.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.-614+4354dupC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422943 | |||||||
| chr22:37422943 | CG | C | 19 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0003g0086 others(16): Show |
19 | HG01099.hp2 HG01257.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-614+4354delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422943 | |||||||
| chr22:37422943 | CGGGG | C | 20 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0135 others(17): Show |
20 | HG01516.hp1 HG01884.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-614+4351_-614+435 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422943 | |||||||
| chr22:37422945 | G | C | 4 | a0001c0002t0088g0285 a0001c0010t0016g0284 a0001c0010t0016g0291 others(1): Show |
4 | HG01891.hp1 HG02145.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-614+4353C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422945 | |||||||
| chr22:37422945 | G | GC | 7 | a0001c0001t0053g0090 a0001c0002t0004g0089 a0001c0002t0004g0092 others(4): Show |
7 | HG00735.hp1 HG02602.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.-614+4352_-614+435 others(5): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422945 | |||||||
| chr22:37422946 | G | C | 41 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0105 others(38): Show |
41 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.-614+4352C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422946 | |||||||
| chr22:37422947 | G | C | 1 | a0001c0002t0021g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-614+4351C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422947 | |||||||
| chr22:37422948 | G | C | 1 | a0001c0003t0001g0018 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-614+4350C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422948 | |||||||
| chr22:37422948 | G | T | 1 | a0001c0002t0004g0029 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-614+4350C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422948 | |||||||
| chr22:37422949 | G | T | 1 | a0001c0002t0069g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-614+4349C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422949 | |||||||
| chr22:37422950 | G | A | 5 | a0001c0001t0017g0316 a0001c0002t0036g0318 a0001c0002t0082g0317 others(2): Show |
5 | HG01516.hp1 HG03239.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-614+4348C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422950 | |||||||
| chr22:37422953 | G | C | 1 | a0001c0001t0050g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-614+4345C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422953 | |||||||
| chr22:37422955 | G | C | 1 | a0001c0001t0002g0123 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-614+4343C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422955 | |||||||
| chr22:37422983 | G | A | 11 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0005g0135 others(8): Show |
11 | HG01884.hp1 HG02572.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-614+4315C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37422983 | |||||||
| chr22:37423137 | G | A | 3 | a0001c0001t0005g0203 a0001c0001t0027g0205 a0001c0006t0047g0204 |
3 | HG02055.hp2 HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-614+4161C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423137 | |||||||
| chr22:37423308 | G | A | 1 | a0001c0002t0077g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-614+3990C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423308 | |||||||
| chr22:37423376 | A | C | 2 | a0001c0002t0008g0312 a0001c0002t0022g0311 |
2 | HG02559.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-614+3922T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423376 | |||||||
| chr22:37423604 | C | T | 1 | a0001c0003t0001g0028 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-614+3694G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423604 | |||||||
| chr22:37423687 | T | A | 3 | a0001c0001t0005g0203 a0001c0001t0027g0205 a0001c0006t0047g0204 |
3 | HG02055.hp2 HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-614+3611A>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423687 | |||||||
| chr22:37423754 | A | T | 1 | a0001c0001t0051g0027 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-614+3544T>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423754 | |||||||
| chr22:37423795 | G | C | 1 | a0001c0001t0005g0165 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-614+3503C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423795 | |||||||
| chr22:37423911 | G | C | 1 | a0001c0002t0004g0286 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-614+3387C>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423911 | |||||||
| chr22:37423947 | G | T | 5 | a0001c0001t0003g0242 a0001c0001t0003g0244 a0001c0003t0012g0245 others(2): Show |
5 | HG00140.hp1 HG00733.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.-614+3351C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37423947 | |||||||
| chr22:37424039 | G | A | 22 | a0001c0001t0005g0149 a0001c0001t0005g0151 a0001c0001t0005g0152 others(19): Show |
22 | HG01109.hp1 HG01516.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-614+3259C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424039 | |||||||
| chr22:37424377 | T | C | 9 | a0001c0001t0017g0316 a0001c0002t0008g0312 a0001c0002t0022g0311 others(6): Show |
9 | HG01516.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+2921A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424377 | |||||||
| chr22:37424592 | A | C | 2 | a0001c0001t0017g0128 a0001c0019t0030g0127 |
2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-614+2706T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424592 | |||||||
| chr22:37424630 | G | A | 3 | a0001c0001t0002g0126 a0001c0003t0001g0124 a0001c0003t0001g0125 |
3 | HG00735.hp2 HG00741.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-614+2668C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424630 | |||||||
| chr22:37424680 | CG | C | 79 | a0001c0001t0002g0005 a0001c0001t0002g0129 a0001c0001t0002g0248 others(76): Show |
81 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.-614+2617delC | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424680 | |||||||
| chr22:37424682 | G | T | 23 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(20): Show |
23 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.-614+2616C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424682 | |||||||
| chr22:37424684 | G | GC | 3 | a0001c0001t0005g0203 a0001c0001t0027g0205 a0001c0006t0047g0204 |
3 | HG02055.hp2 HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-614+2613_-614+261 others(5): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424684 | |||||||
| chr22:37424684 | G | T | 2 | a0001c0002t0033g0025 a0001c0003t0001g0026 |
2 | HG02015.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-614+2614C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424684 | |||||||
| chr22:37424713 | A | AGACAGC | 3 | a0001c0001t0005g0203 a0001c0001t0027g0205 a0001c0006t0047g0204 |
3 | HG02055.hp2 HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-614+2579_-614+258 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424713 | |||||||
| chr22:37424776 | C | T | 66 | a0001c0001t0002g0005 a0001c0001t0002g0240 a0001c0001t0002g0241 others(63): Show |
68 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.-614+2522G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424776 | |||||||
| chr22:37424814 | G | A | 1 | a0001c0003t0012g0303 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-614+2484C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424814 | |||||||
| chr22:37424947 | G | A | 1 | a0001c0002t0007g0304 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-614+2351C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424947 | |||||||
| chr22:37424947 | G | GC | 9 | a0001c0001t0017g0316 a0001c0002t0008g0312 a0001c0002t0022g0311 others(6): Show |
9 | HG01516.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+2350dupG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424947 | |||||||
| chr22:37424949 | C | T | 1 | a0001c0001t0005g0149 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-614+2349G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37424949 | |||||||
| chr22:37425055 | T | G | 1 | a0001c0002t0004g0200 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-614+2243A>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425055 | |||||||
| chr22:37425245 | A | C | 25 | a0001c0001t0005g0149 a0001c0001t0005g0151 a0001c0001t0005g0152 others(22): Show |
25 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-614+2053T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425245 | |||||||
| chr22:37425402 | G | A | 1 | a0001c0001t0097g0321 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-614+1896C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425402 | |||||||
| chr22:37425587 | GC | G | 68 | a0001c0001t0003g0004 a0001c0001t0003g0179 a0001c0001t0003g0182 others(65): Show |
69 | HG00099.hp2 HG00423.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-614+1710delG | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425587 | |||||||
| chr22:37425777 | A | G | 1 | a0001c0003t0001g0178 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-614+1521T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425777 | |||||||
| chr22:37425783 | A | G | 1 | a0001c0002t0069g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-614+1515T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425783 | |||||||
| chr22:37425830 | C | T | 1 | a0001c0002t0021g0148 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-614+1468G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425830 | |||||||
| chr22:37425870 | T | TAC | 4 | a0001c0001t0003g0140 a0001c0002t0004g0139 a0001c0002t0006g0137 others(1): Show |
4 | HG03490.hp1 HG03831.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-614+1426_-614+142 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | |||||||
| chr22:37425870 | T | TACAC | 14 | a0001c0001t0005g0165 a0001c0001t0050g0146 a0001c0001t0099g0328 others(11): Show |
14 | HG00140.hp2 HG01257.hp2 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-614+1424_-614+142 others(8): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | |||||||
| chr22:37425870 | T | TACACAC | 47 | a0001c0001t0003g0004 a0001c0001t0003g0179 a0001c0001t0003g0182 others(44): Show |
48 | HG00099.hp2 HG00642.hp2 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.-614+1422_-614+142 others(10): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | |||||||
| chr22:37425870 | T | TACACACA others(1): Show |
71 | a0001c0001t0002g0005 a0001c0001t0002g0240 a0001c0001t0002g0241 others(68): Show |
73 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-614+1420_-614+142 others(12): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | |||||||
| chr22:37425870 | T | TACACACA others(3): Show |
27 | a0001c0001t0002g0294 a0001c0001t0002g0296 a0001c0001t0002g0301 others(24): Show |
27 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.-614+1418_-614+142 others(14): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | |||||||
| chr22:37425870 | T | TACACACA others(5): Show |
2 | a0001c0002t0066g0233 a0001c0006t0056g0221 |
2 | HG01496.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-614+1416_-614+142 others(16): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | |||||||
| chr22:37425870 | T | TACACACA others(7): Show |
4 | a0001c0001t0009g0306 a0001c0001t0028g0307 a0001c0001t0064g0305 others(1): Show |
4 | HG02258.hp2 HG02818.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-614+1414_-614+142 others(18): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | |||||||
| chr22:37425870 | TAC | T | 9 | a0001c0001t0017g0316 a0001c0002t0004g0023 a0001c0002t0008g0312 others(6): Show |
9 | HG01516.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+1426_-614+142 others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425870 | |||||||
| chr22:37425945 | G | A | 1 | a0001c0003t0001g0141 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-614+1353C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425945 | |||||||
| chr22:37425957 | G | A | 1 | a0001c0001t0003g0222 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-614+1341C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37425957 | |||||||
| chr22:37426013 | A | C | 176 | a0001c0001t0002g0005 a0001c0001t0002g0240 a0001c0001t0002g0241 others(173): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.-614+1285T>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426013 | |||||||
| chr22:37426103 | G | T | 1 | a0001c0002t0079g0237 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-614+1195C>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426103 | |||||||
| chr22:37426178 | C | T | 166 | a0001c0001t0002g0005 a0001c0001t0002g0240 a0001c0001t0002g0241 others(163): Show |
169 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.-614+1120G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426178 | |||||||
| chr22:37426281 | C | T | 1 | a0001c0002t0004g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-614+1017G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426281 | |||||||
| chr22:37426288 | C | T | 25 | a0001c0001t0005g0149 a0001c0001t0005g0151 a0001c0001t0005g0152 others(22): Show |
25 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-614+1010G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426288 | |||||||
| chr22:37426338 | A | G | 140 | a0001c0001t0002g0031 a0001c0001t0002g0043 a0001c0001t0002g0052 others(137): Show |
143 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.-614+960T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426338 | |||||||
| chr22:37426340 | GCA | G | 4 | a0001c0001t0005g0020 a0001c0001t0005g0021 a0001c0001t0009g0019 others(1): Show |
4 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-614+956_-614+957d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426340 | |||||||
| chr22:37426344 | A | ACG | 9 | a0001c0002t0004g0012 a0001c0002t0004g0016 a0001c0002t0004g0147 others(6): Show |
9 | HG00544.hp1 HG00621.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+952_-614+953d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426344 | |||||||
| chr22:37426344 | ACG | A | 12 | a0001c0001t0003g0225 a0001c0001t0005g0226 a0001c0001t0009g0228 others(9): Show |
12 | HG01109.hp2 HG02486.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.-614+952_-614+953d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426344 | |||||||
| chr22:37426356 | G | GCA | 9 | a0001c0001t0017g0316 a0001c0002t0008g0312 a0001c0002t0022g0311 others(6): Show |
9 | HG01516.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-614+940_-614+941d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426356 | |||||||
| chr22:37426356 | GCA | G | 74 | a0001c0001t0002g0005 a0001c0001t0002g0240 a0001c0001t0002g0241 others(71): Show |
76 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.-614+940_-614+941d others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426356 | |||||||
| chr22:37426358 | A | G | 3 | a0001c0002t0069g0142 a0001c0002t0090g0309 a0001c0004t0010g0310 |
3 | HG01099.hp1 HG01099.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-614+940T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426358 | |||||||
| chr22:37426517 | C | T | 1 | a0001c0003t0001g0235 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-614+781G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426517 | |||||||
| chr22:37426615 | A | G | 2 | a0001c0001t0050g0146 a0001c0003t0094g0011 |
2 | HG02622.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-614+683T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426615 | |||||||
| chr22:37426632 | C | T | 1 | a0001c0003t0001g0235 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-614+666G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426632 | |||||||
| chr22:37426650 | AACAC | A | 87 | a0001c0001t0002g0005 a0001c0001t0002g0240 a0001c0001t0002g0241 others(84): Show |
89 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.-614+644_-614+647d others(6): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426650 | |||||||
| chr22:37426800 | A | G | 2 | a0001c0002t0039g0009 a0001c0002t0040g0010 |
2 | NA18949.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.-614+498T>C | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37426800 | |||||||
| chr22:37427023 | T | C | 1 | a0002c0007t0072g0320 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-614+275A>G | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427023 | |||||||
| chr22:37427057 | G | GCCTCCGC others(18): Show |
1 | a0001c0001t0097g0321 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-614+216_-614+240d others(27): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427057 | |||||||
| chr22:37427068 | C | A | 1 | a0001c0003t0044g0326 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-614+230G>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427068 | |||||||
| chr22:37427122 | G | A | 5 | a0001c0001t0025g0323 a0001c0001t0063g0322 a0001c0002t0004g0325 others(2): Show |
5 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-614+176C>T | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427122 | |||||||
| chr22:37427169 | C | T | 3 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0002t0018g0001 |
4 | HG01167.hp2 HG01169.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-614+129G>A | ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427169 | |||||||
| chr22:37427253 | CCGGT | C | 183 | a0001c0001t0002g0005 a0001c0001t0002g0240 a0001c0001t0002g0241 others(180): Show |
186 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.-614+41_-614+44del others(4): Show |
ELFN2 | ENSG00000166897.16 | transcript | ENST00000402918.7 | protein_coding | 1/2 | chr22 | 37427253 |