Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1997 |
| ensemblid | ENSG00000120690.16 |
| hgncid | 3316 |
| symbol | ELF1 |
| name | E74 like ETS transcription factor 1 |
| refseq_nuc | NM_172373.4 |
| refseq_prot | NP_758961.1 |
| ensembl_nuc | ENST00000239882.7 |
| ensembl_prot | ENSP00000239882.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 40931924 |
| end | 41019316 |
| strand | - |
| ver | v1.2 |
| region | chr13:40931924-41019316 |
| region5000 | chr13:40926924-41024316 |
| regionname0 | ELF1_chr13_40931924_41019316 |
| regionname5000 | ELF1_chr13_40926924_41024316 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 619 | 233 | 51 | 18 | 141 | 6 | 15 | 110 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0002 | 0/0 | 619 | 95 | 5 | 33 | 38 | 6 | 13 | 31 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0003 | 0/0 | 619 | 15 | 5 | 0 | 7 | 0 | 3 | 6 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0004 | 0/0 | 619 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0005 | 0/0 | 619 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0006 | 0/0 | 619 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0007 | 0/0 | 619 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0008 | 0/0 | 619 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0009 | 0/0 | 619 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0010 | 0/0 | 619 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0011 | 0/0 | 619 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| a0012 | 0/0 | 619 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | MAAVV others(614): Show |
chr13 | 40926924 | 41024316 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1857 | 175 | 38 | 10 | 112 | 1 | 13 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0001c0003 | 0/1 | 1857 | 46 | 13 | 8 | 18 | 5 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0001c0005 | 0/0 | 1857 | 10 | 0 | 0 | 9 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0001c0013 | 0/0 | 1857 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0001c0014 | 0/0 | 1857 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0002c0002 | 0/0 | 1857 | 95 | 5 | 33 | 38 | 6 | 13 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0003c0004 | 0/0 | 1857 | 13 | 5 | 0 | 6 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0003c0016 | 0/0 | 1857 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0003c0018 | 0/0 | 1857 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0004c0006 | 0/0 | 1857 | 8 | 6 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0005c0007 | 0/0 | 1857 | 3 | 0 | 0 | 3 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0006c0008 | 0/0 | 1857 | 2 | 2 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0007c0015 | 0/0 | 1857 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0008c0017 | 0/0 | 1857 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0009c0010 | 0/0 | 1857 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0010c0009 | 0/0 | 1857 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0011c0011 | 0/0 | 1857 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 | ||
| a0012c0012 | 0/0 | 1857 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | ATGGC others(1852): Show |
chr13 | 40926924 | 41024316 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3678 | 160 | 28 | 10 | 110 | 1 | 10 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0001t0002 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0001t0005 | 0/0 | 3678 | 4 | 4 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0001t0007 | 0/0 | 3678 | 2 | 0 | 0 | 0 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0001t0008 | 0/0 | 3678 | 2 | 2 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0001t0009 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0001t0010 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0001t0011 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0001t0013 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0001t0014 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0001t0015 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0003t0001 | 0/1 | 3678 | 45 | 12 | 8 | 18 | 5 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0003t0012 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0005t0003 | 0/0 | 3678 | 10 | 0 | 0 | 9 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0013t0001 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0001c0014t0001 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0002c0002t0002 | 0/0 | 3678 | 95 | 5 | 33 | 38 | 6 | 13 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0003c0004t0001 | 0/0 | 3678 | 13 | 5 | 0 | 6 | 0 | 2 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0003c0016t0001 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0003c0018t0003 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0004c0006t0004 | 0/0 | 3678 | 8 | 6 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0005c0007t0001 | 0/0 | 3678 | 3 | 0 | 0 | 3 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0006c0008t0006 | 0/0 | 3673 | 2 | 2 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3668): Show |
chr13 | 40926924 | 41024316 |
| a0007c0015t0002 | 0/0 | 3678 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0008c0017t0004 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0009c0010t0001 | 0/0 | 3678 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0010c0009t0006 | 0/0 | 3673 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3668): Show |
chr13 | 40926924 | 41024316 |
| a0011c0011t0001 | 0/0 | 3678 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| a0012c0012t0001 | 0/0 | 3678 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | AATCT others(3673): Show |
chr13 | 40926924 | 41024316 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0007g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0007g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0008g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0010g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0011g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0013g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0014g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0001t0015g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0003t0012g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0005t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0013t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0001c0014t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0002c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0004t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0016t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0003c0018t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0004c0006t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0005c0007t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0005c0007t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0005c0007t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0006c0008t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0006c0008t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0007c0015t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0008c0017t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0009c0010t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0010c0009t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0011c0011t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| a0012c0012t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0208 | EUR | GBR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0097 | EUR | GBR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0168 | EUR | GBR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0213 | EUR | GBR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0030 | EUR | FIN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0098 | EUR | FIN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00408 | hp1 | a0001 | c0001 | t0010 | g0243 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00423 | hp2 | a0003 | c0004 | t0001 | g0198 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00438 | hp1 | a0001 | c0014 | t0001 | g0298 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00597 | hp2 | a0001 | c0003 | t0001 | g0157 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0100 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0199 | EAS | CHS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00733 | hp1 | a0001 | c0003 | t0001 | g0167 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0043 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0322 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0024 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0214 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG00741 | hp2 | a0001 | c0003 | t0001 | g0159 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01070 | hp1 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0029 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0016 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0215 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0317 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0096 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0319 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01192 | hp2 | a0004 | c0006 | t0004 | g0334 | AMR | PUR | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0044 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0205 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01258 | hp2 | a0007 | c0015 | t0002 | g0025 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0031 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01358 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0032 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0045 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0209 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01496 | hp2 | a0004 | c0006 | t0004 | g0010 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0163 | EUR | IBS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0033 | EUR | IBS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0054 | EUR | IBS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0162 | EUR | IBS | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0206 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0021 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02015 | hp2 | a0005 | c0007 | t0001 | g0148 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0178 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0181 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0082 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02083 | hp2 | a0001 | c0001 | t0011 | g0326 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0143 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0252 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CDX | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CDX | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02280 | hp2 | a0008 | c0017 | t0004 | g0050 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0052 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0217 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0349 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0017 | AMR | PEL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0282 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0350 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02572 | hp2 | a0006 | c0008 | t0006 | g0160 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0325 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02630 | hp1 | a0004 | c0006 | t0004 | g0177 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0284 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0056 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02683 | hp2 | a0003 | c0018 | t0003 | g0026 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0046 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02717 | hp1 | a0004 | c0006 | t0004 | g0333 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0049 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02723 | hp2 | a0004 | c0006 | t0004 | g0012 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02738 | hp1 | a0009 | c0010 | t0001 | g0307 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0074 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0094 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02895 | hp2 | a0006 | c0008 | t0006 | g0161 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02922 | hp1 | a0003 | c0004 | t0001 | g0224 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02922 | hp2 | a0004 | c0006 | t0004 | g0331 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02965 | hp1 | a0003 | c0004 | t0001 | g0225 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0114 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0110 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03098 | hp2 | a0010 | c0009 | t0006 | g0296 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0171 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03195 | hp2 | a0004 | c0006 | t0004 | g0332 | AFR | ESN | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03225 | hp1 | a0004 | c0006 | t0004 | g0330 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0072 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03453 | hp2 | a0011 | c0011 | t0001 | g0274 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0172 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03491 | hp1 | a0001 | c0001 | t0007 | g0344 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03491 | hp2 | a0003 | c0004 | t0001 | g0182 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0053 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03492 | hp2 | a0003 | c0004 | t0001 | g0212 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0108 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0216 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0036 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0210 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03834 | hp2 | a0001 | c0005 | t0003 | g0340 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0109 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03942 | hp2 | a0001 | c0001 | t0013 | g0281 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0228 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04184 | hp2 | a0001 | c0003 | t0001 | g0127 | SAS | BEB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0051 | SAS | STU | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18522 | hp2 | a0003 | c0004 | t0001 | g0226 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18612 | hp1 | a0001 | c0005 | t0003 | g0343 | EAS | CHB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18612 | hp2 | a0001 | c0003 | t0001 | g0173 | EAS | CHB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18906 | hp1 | a0003 | c0004 | t0001 | g0227 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0164 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0154 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18946 | hp1 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18948 | hp2 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18950 | hp1 | a0001 | c0005 | t0003 | g0336 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0156 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18953 | hp1 | a0005 | c0007 | t0001 | g0099 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18960 | hp1 | a0001 | c0005 | t0003 | g0337 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18960 | hp2 | a0003 | c0016 | t0001 | g0057 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0169 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18963 | hp1 | a0012 | c0012 | t0001 | g0118 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18963 | hp2 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18964 | hp2 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18966 | hp1 | a0001 | c0005 | t0003 | g0241 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18970 | hp1 | a0001 | c0005 | t0003 | g0342 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18972 | hp2 | a0001 | c0013 | t0001 | g0136 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18982 | hp2 | a0001 | c0003 | t0001 | g0312 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18983 | hp1 | a0003 | c0004 | t0001 | g0193 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18986 | hp2 | a0001 | c0005 | t0003 | g0338 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18988 | hp2 | a0003 | c0004 | t0001 | g0008 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0323 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0351 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0318 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18998 | hp1 | a0001 | c0003 | t0001 | g0303 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19001 | hp2 | a0001 | c0005 | t0003 | g0341 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19004 | hp1 | a0001 | c0005 | t0003 | g0339 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19006 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0153 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0175 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0048 | AFR | LWK | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0324 | AFR | LWK | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19054 | hp1 | a0001 | c0003 | t0001 | g0295 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19062 | hp1 | a0001 | c0003 | t0001 | g0155 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19064 | hp1 | a0003 | c0004 | t0001 | g0204 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19065 | hp2 | a0001 | c0003 | t0001 | g0170 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19066 | hp2 | a0001 | c0003 | t0001 | g0294 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19070 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19075 | hp2 | a0003 | c0004 | t0001 | g0192 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19082 | hp2 | a0001 | c0005 | t0003 | g0101 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19087 | hp1 | a0005 | c0007 | t0001 | g0076 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0235 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0251 | AFR | YRI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ASW | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20129 | hp2 | a0001 | c0003 | t0012 | g0081 | AFR | ASW | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0004 | EUR | TSI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0221 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0035 | AMR | CLM | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02109 | hp2 | a0003 | c0004 | t0001 | g0230 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0011 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | MSL | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | USA | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0047 | AFR | USA | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA20300 | hp2 | a0001 | c0001 | t0014 | g0283 | AFR | USA | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0180 | AFR | LWK | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0063 | REF | REF | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0113 | REF | REF | ELF1_chr13_40926924_41024316 | ELF1 | chr13 | 40926924 | 41024316 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:40933830 | C | T | 1 | a0011 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1455G>A | p.Met485Ile | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1772/3678 | 1455/1860 | 485/619 | chr13 | 40933830 | |||
| chr13:40933871 | G | T | 1 | a0009 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.1414C>A | p.Pro472Thr | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1731/3678 | 1414/1860 | 472/619 | chr13 | 40933871 | |||
| chr13:40933913 | A | G | 1 | a0005 | 3 | HG02015.hp2 NA18953.hp1 NA19087.hp1 |
missense_variant | MODERATE | c.1372T>C | p.Ser458Pro | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1689/3678 | 1372/1860 | 458/619 | chr13 | 40933913 | |||
| chr13:40940969 | G | A | 2 | a0004 a0008 |
9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
missense_variant | MODERATE | c.1208C>T | p.Thr403Ile | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1525/3678 | 1208/1860 | 403/619 | chr13 | 40940969 | |||
| chr13:40941088 | T | G | 1 | a0012 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.1089A>C | p.Gln363His | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1406/3678 | 1089/1860 | 363/619 | chr13 | 40941088 | |||
| chr13:40941129 | A | C | 1 | a0007 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.1048T>G | p.Ser350Ala | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1365/3678 | 1048/1860 | 350/619 | chr13 | 40941129 | |||
| chr13:40941150 | T | A | 4 | a0002 a0006 a0007 others(1): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
missense_variant | MODERATE | c.1027A>T | p.Thr343Ser | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1344/3678 | 1027/1860 | 343/619 | chr13 | 40941150 | |||
| chr13:40958907 | A | G | 1 | a0010 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.182T>C | p.Ile61Thr | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/9 | 499/3678 | 182/1860 | 61/619 | chr13 | 40958907 | |||
| chr13:40958916 | T | C | 4 | a0002 a0003 a0007 others(1): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
missense_variant | MODERATE | c.173A>G | p.Asn58Ser | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/9 | 490/3678 | 173/1860 | 58/619 | chr13 | 40958916 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:40941046 | T | C | 2 | a0001c0005 a0003c0018 |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
synonymous_variant | LOW | c.1131A>G | p.Pro377Pro | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1448/3678 | 1131/1860 | 377/619 | chr13 | 40941046 | |||
| chr13:40941223 | T | A | 1 | a0001c0013 | 1 | NA18972.hp2 | synonymous_variant | LOW | c.954A>T | p.Ser318Ser | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1271/3678 | 954/1860 | 318/619 | chr13 | 40941223 | |||
| chr13:40941232 | T | C | 2 | a0001c0005 a0003c0018 |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
synonymous_variant | LOW | c.945A>G | p.Leu315Leu | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1262/3678 | 945/1860 | 315/619 | chr13 | 40941232 | |||
| chr13:40941235 | C | T | 3 | a0001c0003 a0003c0016 a0005c0007 |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
synonymous_variant | LOW | c.942G>A | p.Ser314Ser | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1259/3678 | 942/1860 | 314/619 | chr13 | 40941235 | |||
| chr13:40941325 | G | A | 1 | a0001c0014 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.852C>T | p.Arg284Arg | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/9 | 1169/3678 | 852/1860 | 284/619 | chr13 | 40941325 | |||
| chr13:40943849 | A | G | 4 | a0002c0002 a0006c0008 a0007c0015 others(1): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
synonymous_variant | LOW | c.606T>C | p.Asp202Asp | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/9 | 923/3678 | 606/1860 | 202/619 | chr13 | 40943849 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:40932094 | C | T | 2 | a0001c0005t0003 a0003c0018t0003 |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1331G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1331 | chr13 | 40932094 | ||||||
| chr13:40932330 | C | G | 1 | a0001c0003t0012 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1095 | chr13 | 40932330 | ||||||
| chr13:40932330 | C | T | 1 | a0001c0001t0011 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1095G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1095 | chr13 | 40932330 | ||||||
| chr13:40932339 | G | T | 1 | a0001c0001t0008 | 2 | HG02145.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1086C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 1086 | chr13 | 40932339 | ||||||
| chr13:40932446 | A | T | 1 | a0001c0001t0007 | 2 | HG03017.hp2 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*979T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 979 | chr13 | 40932446 | ||||||
| chr13:40932585 | C | T | 8 | a0001c0001t0002 a0001c0001t0008 a0001c0005t0003 others(5): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*840G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 840 | chr13 | 40932585 | ||||||
| chr13:40932587 | G | A | 1 | a0001c0001t0013 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*838C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 838 | chr13 | 40932587 | ||||||
| chr13:40932714 | G | T | 2 | a0004c0006t0004 a0008c0017t0004 |
9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*711C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 711 | chr13 | 40932714 | ||||||
| chr13:40932748 | A | G | 7 | a0001c0001t0002 a0001c0005t0003 a0002c0002t0002 others(4): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*677T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 677 | chr13 | 40932748 | ||||||
| chr13:40932783 | A | C | 1 | a0001c0001t0010 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 642 | chr13 | 40932783 | ||||||
| chr13:40932820 | G | T | 1 | a0001c0001t0009 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*605C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 605 | chr13 | 40932820 | ||||||
| chr13:40932849 | T | C | 1 | a0001c0001t0005 | 4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*576A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 576 | chr13 | 40932849 | ||||||
| chr13:40933122 | C | A | 1 | a0001c0001t0014 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*303G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 303 | chr13 | 40933122 | ||||||
| chr13:40933133 | TAGAAA | T | 2 | a0006c0008t0006 a0010c0009t0006 |
3 | HG02572.hp2 HG02895.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*287_*291delTTTCT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 287 | chr13 | 40933133 | ||||||
| chr13:40933225 | C | A | 1 | a0001c0001t0008 | 2 | HG02145.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*200G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 9/9 | 200 | chr13 | 40933225 | ||||||
| chr13:40982189 | T | C | 1 | a0001c0001t0015 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-135A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/9 | 135 | chr13 | 40982189 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:40934171 | T | C | 1 | a0001c0005t0003g0340 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1257-143A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934171 | |||||||
| chr13:40934258 | G | A | 11 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(8): Show |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1257-230C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934258 | |||||||
| chr13:40934415 | G | C | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1257-387C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934415 | |||||||
| chr13:40934416 | C | CT | 8 | a0001c0001t0001g0112 a0001c0001t0015g0011 a0001c0003t0001g0252 others(5): Show |
9 | HG00423.hp2 HG01169.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1257-389dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | |||||||
| chr13:40934416 | C | CTT | 96 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(93): Show |
98 | HG00099.hp1 HG00140.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1257-390_1257-389d others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | |||||||
| chr13:40934416 | C | CTTT | 10 | a0001c0001t0014g0283 a0002c0002t0002g0024 a0002c0002t0002g0030 others(7): Show |
10 | HG00280.hp1 HG00738.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.1257-391_1257-389d others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | |||||||
| chr13:40934416 | CT | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
78 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1257-389delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | |||||||
| chr13:40934416 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0239 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1257-399_1257-389d others(13): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | |||||||
| chr13:40934416 | CTTTTTTT others(5): Show |
C | 89 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(86): Show |
91 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1257-400_1257-389d others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934416 | |||||||
| chr13:40934503 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1257-475C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934503 | |||||||
| chr13:40934577 | C | T | 2 | a0002c0002t0002g0317 a0002c0002t0002g0319 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1257-549G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934577 | |||||||
| chr13:40934578 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1257-550C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934578 | |||||||
| chr13:40934672 | G | A | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1257-644C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934672 | |||||||
| chr13:40934675 | C | A | 1 | a0001c0001t0001g0073 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1257-647G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934675 | |||||||
| chr13:40934708 | C | G | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1257-680G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934708 | |||||||
| chr13:40934715 | C | T | 48 | a0001c0003t0001g0007 a0001c0003t0001g0015 a0001c0003t0001g0016 others(45): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1257-687G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934715 | |||||||
| chr13:40934818 | G | A | 1 | a0012c0012t0001g0118 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1257-790C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40934818 | |||||||
| chr13:40935081 | T | A | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1257-1053A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935081 | |||||||
| chr13:40935174 | A | G | 1 | a0001c0003t0001g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1257-1146T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935174 | |||||||
| chr13:40935177 | G | C | 5 | a0004c0006t0004g0330 a0004c0006t0004g0331 a0004c0006t0004g0332 others(2): Show |
5 | HG01192.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-1149C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935177 | |||||||
| chr13:40935205 | G | T | 1 | a0001c0001t0001g0128 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1257-1177C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935205 | |||||||
| chr13:40935436 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1257-1408A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935436 | |||||||
| chr13:40935509 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1257-1481T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935509 | |||||||
| chr13:40935626 | G | C | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1257-1598C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935626 | |||||||
| chr13:40935675 | A | AT | 12 | a0001c0001t0001g0103 a0001c0001t0001g0112 a0001c0001t0001g0117 others(9): Show |
12 | HG02145.hp1 HG02630.hp2 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.1257-1648dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935675 | |||||||
| chr13:40935675 | A | ATTT | 11 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(8): Show |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1257-1650_1257-164 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935675 | |||||||
| chr13:40935675 | AT | A | 96 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(93): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.1257-1648delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935675 | |||||||
| chr13:40935736 | T | C | 109 | a0001c0001t0002g0111 a0001c0005t0003g0101 a0001c0005t0003g0241 others(106): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.1257-1708A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935736 | |||||||
| chr13:40935797 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0075 |
3 | NA18991.hp2 NA19060.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1257-1769G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935797 | |||||||
| chr13:40935819 | C | A | 11 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(8): Show |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1257-1791G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935819 | |||||||
| chr13:40935910 | T | C | 1 | a0002c0002t0002g0017 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1257-1882A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40935910 | |||||||
| chr13:40936117 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1257-2089G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936117 | |||||||
| chr13:40936188 | T | C | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1257-2160A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936188 | |||||||
| chr13:40936194 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1257-2166A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936194 | |||||||
| chr13:40936203 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(74): Show |
82 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1257-2175C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936203 | |||||||
| chr13:40936219 | A | G | 1 | a0002c0002t0002g0034 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1257-2191T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936219 | |||||||
| chr13:40936440 | C | G | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1257-2412G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936440 | |||||||
| chr13:40936476 | G | A | 1 | a0002c0002t0002g0032 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1257-2448C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936476 | |||||||
| chr13:40936536 | A | G | 112 | a0001c0001t0002g0111 a0001c0001t0008g0143 a0001c0001t0008g0284 others(109): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1257-2508T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936536 | |||||||
| chr13:40936677 | C | T | 108 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(105): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1257-2649G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936677 | |||||||
| chr13:40936693 | G | A | 11 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(8): Show |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1257-2665C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936693 | |||||||
| chr13:40936715 | C | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0272 |
2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1257-2687G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936715 | |||||||
| chr13:40936760 | C | CA | 115 | a0001c0001t0001g0086 a0001c0001t0001g0102 a0001c0001t0001g0103 others(112): Show |
117 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1257-2733dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936760 | |||||||
| chr13:40936760 | C | CAA | 10 | a0001c0005t0003g0341 a0002c0002t0002g0028 a0002c0002t0002g0036 others(7): Show |
10 | HG00621.hp2 HG00735.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1257-2734_1257-273 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936760 | |||||||
| chr13:40936773 | A | G | 2 | a0001c0001t0002g0111 a0001c0001t0015g0011 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1257-2745T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936773 | |||||||
| chr13:40936778 | G | A | 1 | a0002c0002t0002g0054 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1257-2750C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936778 | |||||||
| chr13:40936779 | A | G | 1 | a0002c0002t0002g0054 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1257-2751T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936779 | |||||||
| chr13:40936818 | G | A | 1 | a0002c0002t0002g0221 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1257-2790C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936818 | |||||||
| chr13:40936916 | T | C | 4 | a0001c0005t0003g0336 a0001c0005t0003g0338 a0001c0005t0003g0339 others(1): Show |
4 | NA18950.hp1 NA18986.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.1257-2888A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936916 | |||||||
| chr13:40936953 | CA | C | 4 | a0003c0004t0001g0008 a0003c0004t0001g0192 a0003c0004t0001g0198 others(1): Show |
5 | HG00423.hp2 NA18964.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-2926delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936953 | |||||||
| chr13:40936963 | G | T | 4 | a0003c0004t0001g0008 a0003c0004t0001g0192 a0003c0004t0001g0198 others(1): Show |
5 | HG00423.hp2 NA18964.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.1257-2935C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40936963 | |||||||
| chr13:40937668 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1256+3253T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40937668 | |||||||
| chr13:40937720 | C | T | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+3201G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40937720 | |||||||
| chr13:40937762 | C | T | 9 | a0004c0006t0004g0010 a0004c0006t0004g0012 a0004c0006t0004g0177 others(6): Show |
9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1256+3159G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40937762 | |||||||
| chr13:40937773 | T | C | 2 | a0001c0001t0015g0011 a0011c0011t0001g0274 |
2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1256+3148A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40937773 | |||||||
| chr13:40937976 | C | T | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+2945G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40937976 | |||||||
| chr13:40938018 | T | C | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+2903A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938018 | |||||||
| chr13:40938044 | C | T | 1 | a0002c0002t0002g0199 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1256+2877G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938044 | |||||||
| chr13:40938464 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1256+2457A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938464 | |||||||
| chr13:40938631 | G | A | 1 | a0002c0002t0002g0021 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1256+2290C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938631 | |||||||
| chr13:40938698 | CTTG | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0310 a0001c0001t0001g0311 |
3 | HG03239.hp1 NA18957.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1256+2220_1256+222 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938698 | |||||||
| chr13:40938821 | A | C | 1 | a0002c0002t0002g0206 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1256+2100T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40938821 | |||||||
| chr13:40939112 | T | C | 112 | a0001c0001t0002g0111 a0001c0001t0008g0143 a0001c0001t0008g0284 others(109): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1256+1809A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939112 | |||||||
| chr13:40939246 | T | G | 4 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0094 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1256+1675A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939246 | |||||||
| chr13:40939316 | CA | C | 11 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(8): Show |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1256+1604delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939316 | |||||||
| chr13:40939383 | G | A | 1 | a0011c0011t0001g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1256+1538C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939383 | |||||||
| chr13:40939456 | A | C | 5 | a0003c0004t0001g0224 a0003c0004t0001g0225 a0003c0004t0001g0226 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1256+1465T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939456 | |||||||
| chr13:40939489 | C | T | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+1432G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939489 | |||||||
| chr13:40939546 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1256+1375G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939546 | |||||||
| chr13:40939561 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1256+1360A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939561 | |||||||
| chr13:40939733 | G | C | 1 | a0001c0003t0001g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1256+1188C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939733 | |||||||
| chr13:40939787 | G | A | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+1134C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939787 | |||||||
| chr13:40939980 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0256 a0001c0001t0001g0260 |
5 | NA18949.hp2 NA18983.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1256+941A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40939980 | |||||||
| chr13:40940009 | C | A | 1 | a0002c0002t0002g0233 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1256+912G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940009 | |||||||
| chr13:40940176 | A | G | 38 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0018 others(35): Show |
40 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1256+745T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940176 | |||||||
| chr13:40940282 | C | G | 1 | a0002c0002t0002g0037 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1256+639G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940282 | |||||||
| chr13:40940299 | C | CAGA | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+619_1256+621d others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940299 | |||||||
| chr13:40940309 | T | A | 1 | a0001c0013t0001g0136 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1256+612A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940309 | |||||||
| chr13:40940324 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(92): Show |
97 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.1256+597G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940324 | |||||||
| chr13:40940386 | G | GA | 47 | a0001c0001t0001g0040 a0001c0001t0001g0062 a0001c0001t0001g0077 others(44): Show |
47 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1256+534dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940386 | G | GAA | 13 | a0001c0001t0001g0086 a0001c0001t0001g0102 a0001c0001t0001g0112 others(10): Show |
13 | HG00423.hp2 HG01891.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.1256+533_1256+534d others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940386 | G | GAAA | 6 | a0001c0001t0001g0219 a0001c0001t0001g0246 a0001c0001t0001g0258 others(3): Show |
6 | HG00609.hp1 HG02165.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.1256+532_1256+534d others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940386 | G | GAAAAAA | 5 | a0001c0001t0001g0001 a0001c0001t0001g0236 a0001c0001t0001g0256 others(2): Show |
7 | HG03195.hp1 NA18949.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.1256+529_1256+534d others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940386 | GA | G | 47 | a0001c0001t0001g0069 a0001c0001t0001g0129 a0001c0001t0001g0130 others(44): Show |
47 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.1256+534delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940386 | GAA | G | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(49): Show |
55 | HG00597.hp1 HG00673.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.1256+533_1256+534d others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940386 | GAAA | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0065 a0001c0001t0001g0067 others(14): Show |
17 | HG00408.hp2 HG00544.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.1256+532_1256+534d others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940386 | GAAAA | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0346 a0001c0001t0001g0347 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256+531_1256+534d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940386 | GAAAAAAA others(4): Show |
G | 3 | a0001c0001t0001g0261 a0001c0001t0008g0143 a0001c0001t0008g0284 |
3 | HG02145.hp1 HG02630.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1256+524_1256+534d others(13): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940386 | GAAAAAAA others(5): Show |
G | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+523_1256+534d others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940386 | GAAAAAAA others(10): Show |
G | 9 | a0004c0006t0004g0010 a0004c0006t0004g0012 a0004c0006t0004g0177 others(6): Show |
9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1256+518_1256+534d others(19): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940386 | |||||||
| chr13:40940398 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1256+523T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940398 | |||||||
| chr13:40940408 | A | C | 15 | a0001c0001t0002g0111 a0001c0001t0014g0283 a0001c0001t0015g0011 others(12): Show |
15 | HG02109.hp1 HG02559.hp1 HG02683.hp2 others(12): Show |
intron_variant | MODIFIER | c.1256+513T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940408 | |||||||
| chr13:40940409 | A | C | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+512T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940409 | |||||||
| chr13:40940415 | A | C | 4 | a0001c0003t0001g0078 a0001c0003t0001g0251 a0001c0003t0001g0252 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1256+506T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940415 | |||||||
| chr13:40940418 | A | C | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+503T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940418 | |||||||
| chr13:40940419 | C | A | 3 | a0001c0001t0013g0281 a0001c0003t0001g0082 a0003c0004t0001g0198 |
3 | HG00423.hp2 HG02056.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1256+502G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940419 | |||||||
| chr13:40940456 | G | T | 1 | a0001c0001t0001g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1256+465C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940456 | |||||||
| chr13:40940497 | A | T | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+424T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940497 | |||||||
| chr13:40940560 | A | G | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.1256+361T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940560 | |||||||
| chr13:40940688 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1256+233C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940688 | |||||||
| chr13:40940889 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1256+32T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 8/8 | chr13 | 40940889 | |||||||
| chr13:40941453 | A | C | 1 | a0002c0002t0002g0052 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.807-83T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941453 | |||||||
| chr13:40941482 | G | A | 1 | a0002c0002t0002g0033 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.807-112C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941482 | |||||||
| chr13:40941862 | T | C | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.807-492A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941862 | |||||||
| chr13:40941898 | A | G | 12 | a0001c0001t0002g0111 a0001c0005t0003g0101 a0001c0005t0003g0241 others(9): Show |
12 | HG02109.hp1 HG02683.hp2 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.807-528T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941898 | |||||||
| chr13:40941916 | C | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0277 |
2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.807-546G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941916 | |||||||
| chr13:40941935 | A | G | 53 | a0001c0003t0001g0007 a0001c0003t0001g0015 a0001c0003t0001g0016 others(50): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.807-565T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40941935 | |||||||
| chr13:40942104 | A | C | 1 | a0011c0011t0001g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.807-734T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942104 | |||||||
| chr13:40942303 | T | C | 9 | a0004c0006t0004g0010 a0004c0006t0004g0012 a0004c0006t0004g0177 others(6): Show |
9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.806+649A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942303 | |||||||
| chr13:40942362 | T | C | 1 | a0004c0006t0004g0012 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.806+590A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942362 | |||||||
| chr13:40942386 | G | A | 3 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0328 |
3 | HG02622.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.806+566C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942386 | |||||||
| chr13:40942423 | T | C | 1 | a0001c0001t0001g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.806+529A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942423 | |||||||
| chr13:40942663 | G | A | 1 | a0001c0001t0001g0278 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.806+289C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942663 | |||||||
| chr13:40942732 | G | A | 1 | a0001c0001t0014g0283 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.806+220C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 7/8 | chr13 | 40942732 | |||||||
| chr13:40943159 | A | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0265 |
2 | HG01109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.614-15T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943159 | |||||||
| chr13:40943372 | C | A | 144 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(141): Show |
149 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.614-228G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943372 | |||||||
| chr13:40943382 | A | G | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.614-238T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943382 | |||||||
| chr13:40943405 | G | C | 1 | a0003c0016t0001g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.614-261C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943405 | |||||||
| chr13:40943661 | C | T | 14 | a0001c0001t0002g0111 a0001c0001t0014g0283 a0001c0005t0003g0101 others(11): Show |
14 | HG00609.hp2 HG02109.hp1 HG02683.hp2 others(11): Show |
intron_variant | MODIFIER | c.613+181G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943661 | |||||||
| chr13:40943683 | T | C | 3 | a0005c0007t0001g0076 a0005c0007t0001g0099 a0005c0007t0001g0148 |
3 | HG02015.hp2 NA18953.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.613+159A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 6/8 | chr13 | 40943683 | |||||||
| chr13:40944038 | T | G | 1 | a0001c0001t0001g0246 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.530-113A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944038 | |||||||
| chr13:40944223 | C | G | 53 | a0001c0003t0001g0007 a0001c0003t0001g0015 a0001c0003t0001g0016 others(50): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.530-298G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944223 | |||||||
| chr13:40944467 | C | G | 1 | a0001c0001t0001g0266 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.530-542G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944467 | |||||||
| chr13:40944553 | C | A | 1 | a0002c0002t0002g0223 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.530-628G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944553 | |||||||
| chr13:40944601 | G | A | 3 | a0002c0002t0002g0220 a0002c0002t0002g0222 a0002c0002t0002g0223 |
3 | HG01934.hp1 HG02040.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.530-676C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944601 | |||||||
| chr13:40944602 | T | C | 11 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(8): Show |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.530-677A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944602 | |||||||
| chr13:40944655 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.530-730A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944655 | |||||||
| chr13:40944696 | G | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(165): Show |
175 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.530-771C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944696 | |||||||
| chr13:40944732 | A | G | 4 | a0001c0003t0001g0156 a0001c0003t0001g0157 a0001c0003t0001g0176 others(1): Show |
4 | HG00597.hp2 NA18948.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.530-807T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944732 | |||||||
| chr13:40944783 | T | C | 38 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0018 others(35): Show |
40 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.530-858A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944783 | |||||||
| chr13:40944812 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.530-887C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40944812 | |||||||
| chr13:40945006 | A | C | 11 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(8): Show |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.530-1081T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40945006 | |||||||
| chr13:40945191 | T | C | 9 | a0004c0006t0004g0010 a0004c0006t0004g0012 a0004c0006t0004g0177 others(6): Show |
9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.530-1266A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40945191 | |||||||
| chr13:40945524 | T | C | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.530-1599A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40945524 | |||||||
| chr13:40945950 | T | G | 1 | a0001c0003t0001g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.530-2025A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40945950 | |||||||
| chr13:40946036 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(88): Show |
93 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.530-2111A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946036 | |||||||
| chr13:40946059 | G | A | 1 | a0001c0003t0001g0127 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.530-2134C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946059 | |||||||
| chr13:40946086 | G | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0245 |
3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.530-2161C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946086 | |||||||
| chr13:40946158 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0075 |
3 | NA18991.hp2 NA19060.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.530-2233A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946158 | |||||||
| chr13:40946374 | T | C | 9 | a0004c0006t0004g0010 a0004c0006t0004g0012 a0004c0006t0004g0177 others(6): Show |
9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.530-2449A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946374 | |||||||
| chr13:40946381 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.530-2456A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946381 | |||||||
| chr13:40946648 | G | A | 1 | a0002c0002t0002g0004 | 2 | HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.530-2723C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946648 | |||||||
| chr13:40946783 | T | C | 7 | a0001c0003t0001g0169 a0001c0003t0001g0173 a0001c0003t0001g0174 others(4): Show |
7 | NA18612.hp2 NA18946.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.530-2858A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40946783 | |||||||
| chr13:40947124 | C | CA | 84 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
89 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.529+2681dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40947124 | |||||||
| chr13:40947142 | T | C | 9 | a0004c0006t0004g0010 a0004c0006t0004g0012 a0004c0006t0004g0177 others(6): Show |
9 | HG01192.hp2 HG01496.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.529+2664A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40947142 | |||||||
| chr13:40947393 | T | C | 65 | a0001c0001t0001g0120 a0001c0001t0001g0158 a0001c0001t0014g0283 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.529+2413A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40947393 | |||||||
| chr13:40947681 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.529+2125T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40947681 | |||||||
| chr13:40948104 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.529+1702A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948104 | |||||||
| chr13:40948136 | T | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(74): Show |
82 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.529+1670A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948136 | |||||||
| chr13:40948202 | A | C | 13 | a0002c0002t0002g0019 a0002c0002t0002g0021 a0002c0002t0002g0024 others(10): Show |
13 | HG00099.hp1 HG00140.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.529+1604T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948202 | |||||||
| chr13:40948356 | C | CT | 11 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(8): Show |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+1449dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948356 | |||||||
| chr13:40948366 | C | T | 1 | a0001c0003t0001g0127 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.529+1440G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948366 | |||||||
| chr13:40948402 | T | C | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | NA18951.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.529+1404A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948402 | |||||||
| chr13:40948585 | G | A | 4 | a0001c0001t0001g0117 a0001c0001t0001g0309 a0001c0001t0001g0310 others(1): Show |
4 | HG03239.hp1 NA18957.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.529+1221C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948585 | |||||||
| chr13:40948704 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.529+1102A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948704 | |||||||
| chr13:40948726 | C | CT | 4 | a0001c0001t0001g0103 a0003c0004t0001g0008 a0003c0004t0001g0192 others(1): Show |
5 | HG00423.hp2 NA18964.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+1079_529+1080i others(3): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948726 | |||||||
| chr13:40948856 | G | T | 1 | a0001c0001t0001g0123 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.529+950C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948856 | |||||||
| chr13:40948889 | A | G | 1 | a0002c0002t0002g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.529+917T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40948889 | |||||||
| chr13:40949036 | A | AGTTCAAT others(5): Show |
1 | a0001c0001t0001g0073 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.529+758_529+769dup others(12): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949036 | |||||||
| chr13:40949069 | T | G | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.529+737A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949069 | |||||||
| chr13:40949074 | T | C | 2 | a0001c0003t0001g0007 a0001c0003t0001g0153 |
3 | HG01346.hp1 HG01358.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.529+732A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949074 | |||||||
| chr13:40949118 | T | G | 1 | a0002c0002t0002g0216 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.529+688A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949118 | |||||||
| chr13:40949326 | G | T | 2 | a0001c0003t0001g0015 a0001c0003t0001g0016 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.529+480C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949326 | |||||||
| chr13:40949495 | T | A | 1 | a0001c0001t0001g0278 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.529+311A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949495 | |||||||
| chr13:40949587 | TCAAA | T | 11 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(8): Show |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.529+215_529+218del others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949587 | |||||||
| chr13:40949615 | A | G | 59 | a0001c0001t0001g0120 a0001c0001t0001g0158 a0001c0001t0001g0315 others(56): Show |
60 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.529+191T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949615 | |||||||
| chr13:40949631 | A | T | 1 | a0002c0002t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.529+175T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949631 | |||||||
| chr13:40949676 | ATT | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0346 a0001c0001t0001g0347 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+128_529+129del others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949676 | |||||||
| chr13:40949740 | T | C | 39 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0018 others(36): Show |
41 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.529+66A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 5/8 | chr13 | 40949740 | |||||||
| chr13:40950029 | C | T | 11 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(8): Show |
11 | HG02683.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.362-56G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950029 | |||||||
| chr13:40950030 | G | A | 1 | a0002c0002t0002g0004 | 2 | HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.362-57C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950030 | |||||||
| chr13:40950087 | T | C | 97 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.362-114A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950087 | |||||||
| chr13:40950393 | A | C | 1 | a0001c0001t0001g0277 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.362-420T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950393 | |||||||
| chr13:40950461 | C | T | 1 | a0002c0002t0002g0033 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.362-488G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950461 | |||||||
| chr13:40950492 | A | AT | 56 | a0001c0001t0001g0120 a0001c0001t0001g0158 a0001c0001t0014g0283 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.362-520dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950492 | |||||||
| chr13:40950492 | AT | A | 6 | a0001c0001t0001g0073 a0002c0002t0002g0107 a0002c0002t0002g0181 others(3): Show |
6 | HG00609.hp2 HG01123.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.362-520delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950492 | |||||||
| chr13:40950537 | C | A | 1 | a0002c0002t0002g0208 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.362-564G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950537 | |||||||
| chr13:40950598 | C | A | 65 | a0001c0001t0001g0038 a0001c0001t0001g0120 a0001c0001t0001g0158 others(62): Show |
66 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.362-625G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950598 | |||||||
| chr13:40950928 | A | G | 6 | a0001c0001t0001g0115 a0001c0001t0001g0140 a0001c0001t0001g0141 others(3): Show |
6 | HG00673.hp1 HG02135.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.361+401T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 4/8 | chr13 | 40950928 | |||||||
| chr13:40951450 | A | G | 98 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(95): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.254-14T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951450 | |||||||
| chr13:40951598 | G | A | 1 | a0002c0002t0002g0107 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.254-162C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951598 | |||||||
| chr13:40951633 | A | G | 98 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(95): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.254-197T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951633 | |||||||
| chr13:40951732 | T | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0346 a0001c0001t0001g0347 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.254-296A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951732 | |||||||
| chr13:40951782 | G | A | 38 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0018 others(35): Show |
40 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.254-346C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951782 | |||||||
| chr13:40951783 | T | C | 98 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(95): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.254-347A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951783 | |||||||
| chr13:40951798 | T | C | 1 | a0001c0003t0001g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.254-362A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951798 | |||||||
| chr13:40951904 | A | G | 1 | a0001c0001t0001g0315 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.254-468T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40951904 | |||||||
| chr13:40952214 | C | T | 75 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(72): Show |
80 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.254-778G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952214 | |||||||
| chr13:40952233 | A | G | 56 | a0001c0001t0001g0120 a0001c0001t0001g0158 a0001c0001t0014g0283 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.254-797T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952233 | |||||||
| chr13:40952286 | A | C | 1 | a0008c0017t0004g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.254-850T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952286 | |||||||
| chr13:40952368 | C | CT | 99 | a0001c0001t0001g0123 a0002c0002t0002g0003 a0002c0002t0002g0004 others(96): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.254-933dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952368 | |||||||
| chr13:40952368 | CT | C | 6 | a0001c0003t0001g0154 a0001c0003t0001g0155 a0001c0003t0001g0166 others(3): Show |
6 | NA18940.hp2 NA18963.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-933delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952368 | |||||||
| chr13:40952395 | C | T | 3 | a0001c0001t0002g0111 a0001c0001t0008g0143 a0001c0001t0008g0284 |
3 | HG02109.hp1 HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.254-959G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952395 | |||||||
| chr13:40952427 | T | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0075 |
3 | NA18991.hp2 NA19060.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.254-991A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952427 | |||||||
| chr13:40952472 | C | T | 35 | a0001c0001t0001g0120 a0001c0001t0001g0158 a0001c0003t0001g0007 others(32): Show |
36 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.254-1036G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952472 | |||||||
| chr13:40952485 | C | T | 3 | a0001c0001t0002g0111 a0001c0001t0008g0143 a0001c0001t0008g0284 |
3 | HG02109.hp1 HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.254-1049G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952485 | |||||||
| chr13:40952511 | G | A | 98 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(95): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.254-1075C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952511 | |||||||
| chr13:40952513 | C | T | 98 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(95): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.254-1077G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952513 | |||||||
| chr13:40952751 | T | C | 1 | a0001c0003t0001g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.254-1315A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952751 | |||||||
| chr13:40952847 | TTACCCTC others(2): Show |
T | 56 | a0001c0001t0001g0120 a0001c0001t0001g0158 a0001c0001t0014g0283 others(53): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.254-1420_254-1412d others(11): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952847 | |||||||
| chr13:40952978 | C | CT | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(318): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.254-1543dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952978 | |||||||
| chr13:40952978 | C | CTT | 8 | a0001c0001t0001g0075 a0001c0001t0001g0266 a0001c0003t0001g0154 others(5): Show |
8 | HG00642.hp1 HG02738.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.254-1544_254-1543d others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40952978 | |||||||
| chr13:40953069 | C | T | 94 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(91): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.254-1633G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953069 | |||||||
| chr13:40953218 | T | C | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.254-1782A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953218 | |||||||
| chr13:40953228 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.254-1792C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953228 | |||||||
| chr13:40953272 | G | A | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.254-1836C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953272 | |||||||
| chr13:40953273 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.254-1837C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953273 | |||||||
| chr13:40953284 | T | G | 1 | a0001c0001t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.254-1848A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953284 | |||||||
| chr13:40953296 | A | G | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.254-1860T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953296 | |||||||
| chr13:40953323 | C | G | 1 | a0001c0001t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.254-1887G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953323 | |||||||
| chr13:40953503 | T | A | 1 | a0002c0002t0002g0221 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.254-2067A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953503 | |||||||
| chr13:40953522 | G | T | 1 | a0002c0002t0002g0221 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.254-2086C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953522 | |||||||
| chr13:40953579 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.254-2143C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953579 | |||||||
| chr13:40953665 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.254-2229C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953665 | |||||||
| chr13:40953757 | T | G | 13 | a0001c0001t0001g0124 a0001c0001t0001g0139 a0001c0005t0003g0101 others(10): Show |
13 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(10): Show |
intron_variant | MODIFIER | c.254-2321A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953757 | |||||||
| chr13:40953882 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.254-2446T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953882 | |||||||
| chr13:40953914 | T | A | 1 | a0002c0002t0002g0186 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.254-2478A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953914 | |||||||
| chr13:40953976 | CAAAGACT others(23): Show |
C | 1 | a0001c0001t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.254-2570_254-2541d others(32): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40953976 | |||||||
| chr13:40954109 | T | C | 2 | a0001c0005t0003g0342 a0001c0005t0003g0343 |
2 | NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.254-2673A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954109 | |||||||
| chr13:40954252 | A | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0258 |
2 | HG02165.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.254-2816T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954252 | |||||||
| chr13:40954268 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.254-2832A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954268 | |||||||
| chr13:40954420 | G | GCTCTCCC others(14): Show |
109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.254-2985_254-2984i others(23): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954420 | |||||||
| chr13:40954421 | CTCTCCCT others(10): Show |
C | 5 | a0001c0001t0001g0134 a0001c0001t0001g0315 a0006c0008t0006g0160 others(2): Show |
5 | HG02572.hp2 HG02895.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.254-3002_254-2986d others(19): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954421 | |||||||
| chr13:40954490 | G | A | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.254-3054C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954490 | |||||||
| chr13:40954580 | T | C | 6 | a0001c0003t0001g0169 a0001c0003t0001g0173 a0001c0003t0001g0174 others(3): Show |
6 | NA18612.hp2 NA18946.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-3144A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954580 | |||||||
| chr13:40954620 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.254-3184C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954620 | |||||||
| chr13:40954753 | A | G | 1 | a0001c0005t0003g0337 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.254-3317T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954753 | |||||||
| chr13:40954754 | A | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
234 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.254-3318T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954754 | |||||||
| chr13:40954777 | T | G | 2 | a0001c0001t0001g0269 a0001c0001t0001g0275 |
2 | HG00609.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.254-3341A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954777 | |||||||
| chr13:40954868 | A | AC | 4 | a0001c0001t0001g0064 a0001c0003t0001g0178 a0002c0002t0002g0051 others(1): Show |
4 | HG02055.hp1 HG04228.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.254-3433dupG | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954868 | |||||||
| chr13:40954890 | C | T | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.254-3454G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954890 | |||||||
| chr13:40954893 | C | T | 1 | a0001c0005t0003g0341 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.254-3457G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954893 | |||||||
| chr13:40954904 | G | C | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.254-3468C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40954904 | |||||||
| chr13:40955007 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.254-3571C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955007 | |||||||
| chr13:40955060 | G | A | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.254-3624C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955060 | |||||||
| chr13:40955064 | T | C | 337 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(334): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.254-3628A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955064 | |||||||
| chr13:40955065 | G | A | 73 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.254-3629C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955065 | |||||||
| chr13:40955077 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.254-3641T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955077 | |||||||
| chr13:40955082 | C | T | 6 | a0001c0001t0001g0239 a0001c0001t0001g0267 a0001c0001t0001g0268 others(3): Show |
6 | HG00609.hp1 NA18952.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-3646G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955082 | |||||||
| chr13:40955093 | G | A | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.254-3657C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955093 | |||||||
| chr13:40955096 | T | C | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.254-3660A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955096 | |||||||
| chr13:40955102 | G | A | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.254-3666C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955102 | |||||||
| chr13:40955136 | C | T | 82 | a0001c0001t0001g0038 a0001c0001t0001g0064 a0001c0001t0001g0065 others(79): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.253+3700G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955136 | |||||||
| chr13:40955140 | G | A | 1 | a0002c0002t0002g0221 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.253+3696C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955140 | |||||||
| chr13:40955205 | C | T | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+3631G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955205 | |||||||
| chr13:40955206 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.253+3630C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955206 | |||||||
| chr13:40955240 | A | G | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.253+3596T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955240 | |||||||
| chr13:40955263 | T | C | 2 | a0001c0003t0001g0166 a0001c0003t0001g0294 |
2 | NA18963.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.253+3573A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955263 | |||||||
| chr13:40955276 | T | TG | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+3559dupC | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955276 | |||||||
| chr13:40955312 | CGGAA | C | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3520_253+3523d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955312 | |||||||
| chr13:40955325 | G | A | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3511C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955325 | |||||||
| chr13:40955329 | GGTTAGCC others(1): Show |
G | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3499_253+3506d others(10): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955329 | |||||||
| chr13:40955339 | C | G | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3497G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955339 | |||||||
| chr13:40955341 | A | C | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3495T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955341 | |||||||
| chr13:40955342 | C | T | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3494G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955342 | |||||||
| chr13:40955344 | C | T | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3492G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955344 | |||||||
| chr13:40955346 | G | C | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3490C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955346 | |||||||
| chr13:40955349 | A | G | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3487T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955349 | |||||||
| chr13:40955352 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.253+3484G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955352 | |||||||
| chr13:40955353 | G | A | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.253+3483C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955353 | |||||||
| chr13:40955358 | A | T | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3478T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955358 | |||||||
| chr13:40955359 | T | A | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3477A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955359 | |||||||
| chr13:40955361 | C | T | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3475G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955361 | |||||||
| chr13:40955366 | G | A | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3470C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955366 | |||||||
| chr13:40955367 | GGAGA | G | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3465_253+3468d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955367 | |||||||
| chr13:40955371 | A | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(324): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.253+3465T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955371 | |||||||
| chr13:40955374 | G | A | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3462C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955374 | |||||||
| chr13:40955377 | G | A | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3459C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955377 | |||||||
| chr13:40955378 | GGTCA | G | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3454_253+3457d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955378 | |||||||
| chr13:40955387 | C | T | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3449G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955387 | |||||||
| chr13:40955393 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(213): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.253+3443G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955393 | |||||||
| chr13:40955394 | G | A | 4 | a0002c0002t0002g0051 a0002c0002t0002g0052 a0002c0002t0002g0053 others(1): Show |
4 | HG01071.hp2 HG02293.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+3442C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955394 | |||||||
| chr13:40955401 | T | C | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3435A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955401 | |||||||
| chr13:40955402 | G | GC | 11 | a0001c0001t0001g0064 a0001c0001t0001g0234 a0001c0001t0001g0236 others(8): Show |
11 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+3433dupG | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955402 | |||||||
| chr13:40955406 | A | G | 119 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(116): Show |
122 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.253+3430T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955406 | |||||||
| chr13:40955416 | G | T | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3420C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955416 | |||||||
| chr13:40955441 | C | T | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+3395G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955441 | |||||||
| chr13:40955450 | G | A | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+3386C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955450 | |||||||
| chr13:40955458 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.253+3378G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955458 | |||||||
| chr13:40955464 | GT | G | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3371delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955464 | |||||||
| chr13:40955470 | G | T | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3366C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955470 | |||||||
| chr13:40955471 | GCGCCTCT others(17): Show |
G | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3341_253+3364d others(26): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955471 | |||||||
| chr13:40955499 | A | G | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3337T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955499 | |||||||
| chr13:40955500 | A | G | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3336T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955500 | |||||||
| chr13:40955503 | G | C | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3333C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955503 | |||||||
| chr13:40955505 | GGAGT | G | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3327_253+3330d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955505 | |||||||
| chr13:40955513 | T | C | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3323A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955513 | |||||||
| chr13:40955515 | T | C | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3321A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955515 | |||||||
| chr13:40955515 | T | TGCCCGGC others(90): Show |
1 | a0001c0005t0003g0340 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.253+3320_253+3321i others(99): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955515 | |||||||
| chr13:40955519 | C | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0009g0235 |
3 | HG02615.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.253+3317G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955519 | |||||||
| chr13:40955528 | G | A | 2 | a0002c0002t0002g0033 a0003c0018t0003g0026 |
2 | HG01516.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.253+3308C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955528 | |||||||
| chr13:40955533 | G | A | 10 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(7): Show |
10 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+3303C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955533 | |||||||
| chr13:40955539 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0346 others(2): Show |
7 | HG01884.hp2 HG01981.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.253+3297C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955539 | |||||||
| chr13:40955541 | A | G | 11 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(8): Show |
11 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+3295T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955541 | |||||||
| chr13:40955543 | T | G | 11 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0001g0239 others(8): Show |
11 | HG00609.hp1 HG01934.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.253+3293A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(93): Show |
2 | a0002c0002t0002g0021 a0002c0002t0002g0186 |
2 | HG01981.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.253+3292_253+3293i others(102): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(93): Show |
1 | a0002c0002t0002g0223 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.253+3292_253+3293i others(102): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(93): Show |
2 | a0002c0002t0002g0209 a0004c0006t0004g0334 |
2 | HG01192.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.253+3292_253+3293i others(102): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(93): Show |
1 | a0002c0002t0002g0039 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.253+3292_253+3293i others(102): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(92): Show |
105 | a0001c0001t0001g0124 a0002c0002t0002g0003 a0002c0002t0002g0004 others(102): Show |
108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.253+3292_253+3293i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(92): Show |
1 | a0001c0003t0001g0157 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.253+3292_253+3293i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(92): Show |
1 | a0001c0001t0001g0149 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.253+3292_253+3293i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(91): Show |
2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(92): Show |
1 | a0001c0001t0001g0123 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.253+3292_253+3293i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(91): Show |
1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(42): Show |
1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.253+3292_253+3293i others(51): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(92): Show |
1 | a0001c0001t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.253+3292_253+3293i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(91): Show |
3 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0167 |
3 | HG00099.hp2 HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(91): Show |
78 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(75): Show |
80 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(91): Show |
68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(65): Show |
73 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(70): Show |
intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955543 | T | TAGGTGGG others(91): Show |
65 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(62): Show |
66 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.253+3292_253+3293i others(100): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955543 | |||||||
| chr13:40955547 | T | TGGGGGGG others(94): Show |
1 | a0002c0002t0002g0059 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.253+3288_253+3289i others(103): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955547 | |||||||
| chr13:40955547 | T | TGGGGGGG others(92): Show |
1 | a0001c0001t0001g0250 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.253+3288_253+3289i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955547 | |||||||
| chr13:40955547 | T | TGGGGGGG others(92): Show |
1 | a0001c0001t0001g0126 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.253+3288_253+3289i others(101): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955547 | |||||||
| chr13:40955558 | G | GCCCCCCG others(93): Show |
1 | a0001c0003t0001g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.253+3277_253+3278i others(102): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955558 | |||||||
| chr13:40955565 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.253+3271T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955565 | |||||||
| chr13:40955586 | G | A | 73 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.253+3250C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955586 | |||||||
| chr13:40955609 | T | C | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+3227A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955609 | |||||||
| chr13:40955637 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
57 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.253+3199G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955637 | |||||||
| chr13:40955655 | G | C | 1 | a0001c0001t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.253+3181C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955655 | |||||||
| chr13:40955660 | G | A | 1 | a0002c0002t0002g0034 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.253+3176C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955660 | |||||||
| chr13:40955669 | G | T | 82 | a0001c0001t0001g0038 a0001c0001t0001g0064 a0001c0001t0001g0065 others(79): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.253+3167C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955669 | |||||||
| chr13:40955710 | T | G | 1 | a0001c0003t0001g0098 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.253+3126A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955710 | |||||||
| chr13:40955728 | A | G | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0245 |
3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3108T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955728 | |||||||
| chr13:40955731 | T | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0247 |
3 | NA18988.hp1 NA19054.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.253+3105A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955731 | |||||||
| chr13:40955745 | G | A | 1 | a0001c0005t0003g0338 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.253+3091C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955745 | |||||||
| chr13:40955753 | G | A | 182 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(179): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.253+3083C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955753 | |||||||
| chr13:40955770 | G | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0245 |
3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3066C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955770 | |||||||
| chr13:40955772 | C | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0245 |
3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3064G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955772 | |||||||
| chr13:40955777 | G | C | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0245 |
3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3059C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955777 | |||||||
| chr13:40955787 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0245 |
3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3049G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955787 | |||||||
| chr13:40955789 | C | CCGCCCGG others(35): Show |
1 | a0009c0010t0001g0307 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.253+3046_253+3047i others(44): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955789 | |||||||
| chr13:40955789 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0245 |
3 | HG02040.hp2 HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.253+3047G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955789 | |||||||
| chr13:40955799 | G | C | 4 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0245 others(1): Show |
4 | HG02040.hp2 HG02523.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.253+3037C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955799 | |||||||
| chr13:40955799 | G | GCCGCCCC others(34): Show |
226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(223): Show |
234 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.253+2996_253+3036d others(43): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955799 | |||||||
| chr13:40955807 | G | GTCCGGGA others(34): Show |
3 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0009g0235 |
3 | HG02615.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.253+3028_253+3029i others(43): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955807 | |||||||
| chr13:40955839 | A | ACCCGCCC others(36): Show |
1 | a0001c0001t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.253+2996_253+2997i others(45): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955839 | |||||||
| chr13:40955840 | C | CCCGCCCC others(33): Show |
1 | a0001c0001t0001g0123 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.253+2995_253+2996i others(42): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955840 | |||||||
| chr13:40955844 | T | G | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2992A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955844 | |||||||
| chr13:40955845 | A | T | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2991T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955845 | |||||||
| chr13:40955847 | T | C | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2989A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955847 | |||||||
| chr13:40955852 | A | G | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2984T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955852 | |||||||
| chr13:40955854 | A | T | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2982T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955854 | |||||||
| chr13:40955859 | A | G | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2977T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955859 | |||||||
| chr13:40955862 | C | G | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2974G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955862 | |||||||
| chr13:40955867 | C | T | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2969G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955867 | |||||||
| chr13:40955885 | A | C | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2951T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955885 | |||||||
| chr13:40955887 | C | A | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2949G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955887 | |||||||
| chr13:40955889 | A | G | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+2947T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955889 | |||||||
| chr13:40955892 | A | T | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2944T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955892 | |||||||
| chr13:40955897 | G | A | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2939C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955897 | |||||||
| chr13:40955899 | C | A | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2937G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955899 | |||||||
| chr13:40955901 | G | A | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2935C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955901 | |||||||
| chr13:40955910 | G | C | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2926C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955910 | |||||||
| chr13:40955914 | C | T | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2922G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955914 | |||||||
| chr13:40955920 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(222): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.253+2916G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955920 | |||||||
| chr13:40955929 | G | A | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2907C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955929 | |||||||
| chr13:40955934 | G | A | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2902C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955934 | |||||||
| chr13:40955938 | G | A | 111 | a0001c0001t0008g0143 a0001c0001t0008g0284 a0002c0002t0002g0003 others(108): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.253+2898C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955938 | |||||||
| chr13:40955938 | G | C | 1 | a0001c0001t0001g0242 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.253+2898C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955938 | |||||||
| chr13:40955938 | G | GGGAGGTG others(71): Show |
1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.253+2897_253+2898i others(80): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955938 | |||||||
| chr13:40955947 | G | GT | 72 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(69): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.253+2888_253+2889i others(3): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955947 | |||||||
| chr13:40955948 | C | G | 73 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.253+2888G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955948 | |||||||
| chr13:40955953 | G | A | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.253+2883C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955953 | |||||||
| chr13:40955959 | G | GC | 72 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(69): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.253+2876dupG | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40955959 | |||||||
| chr13:40956010 | T | C | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+2826A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956010 | |||||||
| chr13:40956028 | A | G | 8 | a0002c0002t0002g0074 a0002c0002t0002g0205 a0002c0002t0002g0206 others(5): Show |
8 | HG01106.hp1 HG01258.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.253+2808T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956028 | |||||||
| chr13:40956047 | C | CGGCCACC others(12): Show |
1 | a0001c0001t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.253+2788_253+2789i others(21): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956047 | |||||||
| chr13:40956065 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.253+2771C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956065 | |||||||
| chr13:40956073 | A | G | 2 | a0001c0001t0001g0315 a0001c0005t0003g0342 |
2 | HG06807.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.253+2763T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956073 | |||||||
| chr13:40956075 | T | C | 2 | a0001c0001t0001g0315 a0001c0005t0003g0342 |
2 | HG06807.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.253+2761A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956075 | |||||||
| chr13:40956078 | A | G | 2 | a0001c0001t0001g0315 a0001c0005t0003g0342 |
2 | HG06807.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.253+2758T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956078 | |||||||
| chr13:40956080 | A | G | 2 | a0001c0001t0001g0315 a0001c0005t0003g0342 |
2 | HG06807.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.253+2756T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956080 | |||||||
| chr13:40956108 | A | G | 2 | a0001c0005t0003g0339 a0001c0005t0003g0341 |
2 | NA19001.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.253+2728T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956108 | |||||||
| chr13:40956113 | G | A | 1 | a0001c0003t0001g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.253+2723C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956113 | |||||||
| chr13:40956153 | C | T | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+2683G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956153 | |||||||
| chr13:40956300 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.253+2536A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956300 | |||||||
| chr13:40956432 | T | G | 1 | a0001c0001t0001g0320 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.253+2404A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956432 | |||||||
| chr13:40956469 | A | G | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+2367T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956469 | |||||||
| chr13:40956516 | C | T | 1 | a0002c0002t0002g0195 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.253+2320G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956516 | |||||||
| chr13:40956571 | C | CA | 6 | a0002c0002t0002g0017 a0002c0002t0002g0048 a0002c0002t0002g0049 others(3): Show |
6 | HG02055.hp2 HG02300.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.253+2264dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956571 | |||||||
| chr13:40956571 | CA | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
67 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.253+2264delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956571 | |||||||
| chr13:40956571 | CAA | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(165): Show |
171 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.253+2263_253+2264d others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956571 | |||||||
| chr13:40956571 | CAAAAAAA | C | 9 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(6): Show |
9 | NA18612.hp1 NA18950.hp1 NA18960.hp1 others(6): Show |
intron_variant | MODIFIER | c.253+2258_253+2264d others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956571 | |||||||
| chr13:40956644 | C | G | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+2192G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956644 | |||||||
| chr13:40956834 | C | T | 8 | a0001c0001t0001g0264 a0001c0001t0001g0301 a0001c0001t0001g0302 others(5): Show |
8 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.253+2002G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956834 | |||||||
| chr13:40956987 | C | T | 1 | a0002c0002t0002g0048 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.253+1849G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40956987 | |||||||
| chr13:40957055 | G | GTCTAAAT others(11): Show |
109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+1780_253+1781i others(20): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957055 | |||||||
| chr13:40957088 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(140): Show |
150 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.253+1748A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957088 | |||||||
| chr13:40957167 | C | T | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+1669G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957167 | |||||||
| chr13:40957508 | TA | T | 8 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0137 others(5): Show |
8 | HG01496.hp2 HG01516.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.253+1327delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957508 | |||||||
| chr13:40957651 | C | T | 52 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
57 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.253+1185G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957651 | |||||||
| chr13:40957822 | C | A | 1 | a0002c0002t0002g0049 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.253+1014G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957822 | |||||||
| chr13:40957880 | T | C | 3 | a0005c0007t0001g0076 a0005c0007t0001g0099 a0005c0007t0001g0148 |
3 | HG02015.hp2 NA18953.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.253+956A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957880 | |||||||
| chr13:40957990 | T | C | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.253+846A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40957990 | |||||||
| chr13:40958290 | T | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+546A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40958290 | |||||||
| chr13:40958330 | A | G | 1 | a0001c0003t0001g0295 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.253+506T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40958330 | |||||||
| chr13:40958381 | C | T | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.253+455G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40958381 | |||||||
| chr13:40958431 | T | A | 1 | a0008c0017t0004g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.253+405A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40958431 | |||||||
| chr13:40958638 | T | C | 4 | a0001c0003t0001g0007 a0001c0003t0001g0153 a0001c0003t0001g0159 others(1): Show |
5 | HG00140.hp1 HG00741.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.253+198A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 3/8 | chr13 | 40958638 | |||||||
| chr13:40959137 | T | C | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.73-121A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959137 | |||||||
| chr13:40959262 | C | G | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-246G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959262 | |||||||
| chr13:40959294 | A | T | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-278T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959294 | |||||||
| chr13:40959322 | C | A | 1 | a0002c0002t0002g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.73-306G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959322 | |||||||
| chr13:40959359 | G | A | 9 | a0001c0001t0001g0239 a0001c0001t0001g0267 a0001c0001t0001g0268 others(6): Show |
9 | HG00609.hp1 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.73-343C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959359 | |||||||
| chr13:40959387 | T | C | 1 | a0001c0003t0001g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.73-371A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959387 | |||||||
| chr13:40959530 | G | A | 11 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(8): Show |
11 | HG00408.hp1 NA18959.hp1 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-514C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959530 | |||||||
| chr13:40959531 | C | A | 11 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(8): Show |
11 | HG00408.hp1 NA18959.hp1 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-515G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959531 | |||||||
| chr13:40959546 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.73-530G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959546 | |||||||
| chr13:40959587 | T | C | 11 | a0001c0001t0015g0011 a0001c0005t0003g0101 a0001c0005t0003g0241 others(8): Show |
11 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-571A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959587 | |||||||
| chr13:40959752 | G | GTATAAAC | 73 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.73-743_73-737dupGT others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959752 | |||||||
| chr13:40959845 | T | C | 82 | a0001c0001t0001g0038 a0001c0001t0001g0064 a0001c0001t0001g0065 others(79): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.73-829A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40959845 | |||||||
| chr13:40960460 | A | G | 1 | a0001c0003t0001g0169 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.73-1444T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40960460 | |||||||
| chr13:40960583 | G | A | 1 | a0001c0003t0001g0175 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.73-1567C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40960583 | |||||||
| chr13:40960808 | G | A | 1 | a0001c0003t0001g0174 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.73-1792C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40960808 | |||||||
| chr13:40960810 | G | C | 9 | a0001c0001t0001g0038 a0004c0006t0004g0010 a0004c0006t0004g0012 others(6): Show |
9 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-1794C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40960810 | |||||||
| chr13:40960902 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(222): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.73-1886C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40960902 | |||||||
| chr13:40961065 | A | G | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-2049T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961065 | |||||||
| chr13:40961152 | TTC | T | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-2138_73-2137del others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961152 | |||||||
| chr13:40961273 | T | A | 59 | a0002c0002t0002g0017 a0002c0002t0002g0019 a0002c0002t0002g0021 others(56): Show |
60 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.73-2257A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961273 | |||||||
| chr13:40961558 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-2542C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961558 | |||||||
| chr13:40961618 | C | T | 3 | a0002c0002t0002g0187 a0002c0002t0002g0194 a0002c0002t0002g0323 |
3 | NA18991.hp1 NA19079.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.73-2602G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961618 | |||||||
| chr13:40961802 | C | G | 1 | a0001c0001t0001g0291 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.73-2786G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961802 | |||||||
| chr13:40961981 | C | T | 5 | a0001c0001t0001g0237 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | NA18962.hp2 NA18972.hp1 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-2965G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40961981 | |||||||
| chr13:40962073 | G | A | 8 | a0004c0006t0004g0010 a0004c0006t0004g0012 a0004c0006t0004g0177 others(5): Show |
8 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-3057C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962073 | |||||||
| chr13:40962396 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(224): Show |
235 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.73-3380T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962396 | |||||||
| chr13:40962463 | A | G | 73 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.73-3447T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962463 | |||||||
| chr13:40962520 | T | C | 1 | a0001c0001t0013g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.73-3504A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962520 | |||||||
| chr13:40962679 | C | CA | 12 | a0001c0001t0001g0038 a0001c0001t0001g0077 a0001c0003t0001g0324 others(9): Show |
12 | HG01192.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.73-3664dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962679 | |||||||
| chr13:40962694 | A | G | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-3678T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962694 | |||||||
| chr13:40962995 | C | T | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-3979G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40962995 | |||||||
| chr13:40963178 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-4162A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963178 | |||||||
| chr13:40963312 | T | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-4296A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963312 | |||||||
| chr13:40963421 | C | T | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-4405G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963421 | |||||||
| chr13:40963549 | C | A | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.73-4533G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963549 | |||||||
| chr13:40963556 | C | G | 2 | a0003c0004t0001g0227 a0003c0004t0001g0230 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.73-4540G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963556 | |||||||
| chr13:40963633 | G | C | 2 | a0003c0004t0001g0227 a0003c0004t0001g0230 |
2 | HG02109.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.73-4617C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963633 | |||||||
| chr13:40963686 | A | G | 1 | a0002c0002t0002g0051 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.73-4670T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963686 | |||||||
| chr13:40963715 | T | C | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-4699A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963715 | |||||||
| chr13:40963735 | T | G | 1 | a0002c0002t0002g0034 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.73-4719A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963735 | |||||||
| chr13:40963820 | T | C | 9 | a0001c0001t0001g0038 a0004c0006t0004g0010 a0004c0006t0004g0012 others(6): Show |
9 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-4804A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963820 | |||||||
| chr13:40963837 | C | T | 5 | a0003c0004t0001g0224 a0003c0004t0001g0225 a0003c0004t0001g0226 others(2): Show |
5 | HG02109.hp2 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-4821G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963837 | |||||||
| chr13:40963911 | G | GA | 7 | a0001c0001t0001g0299 a0002c0002t0002g0043 a0002c0002t0002g0044 others(4): Show |
7 | HG00733.hp2 HG00738.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-4896dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40963911 | |||||||
| chr13:40964053 | C | T | 1 | a0002c0002t0002g0107 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.73-5037G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964053 | |||||||
| chr13:40964111 | C | T | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.73-5095G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964111 | |||||||
| chr13:40964123 | A | G | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-5107T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964123 | |||||||
| chr13:40964280 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.73-5264A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964280 | |||||||
| chr13:40964298 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.73-5282C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964298 | |||||||
| chr13:40964516 | C | CT | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.73-5501dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964516 | |||||||
| chr13:40964598 | A | G | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.73-5582T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964598 | |||||||
| chr13:40964817 | G | A | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-5801C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40964817 | |||||||
| chr13:40965031 | A | G | 1 | a0001c0003t0001g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.73-6015T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965031 | |||||||
| chr13:40965290 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.73-6274G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965290 | |||||||
| chr13:40965344 | G | A | 8 | a0004c0006t0004g0010 a0004c0006t0004g0012 a0004c0006t0004g0177 others(5): Show |
8 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-6328C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965344 | |||||||
| chr13:40965592 | A | G | 11 | a0001c0001t0015g0011 a0001c0005t0003g0101 a0001c0005t0003g0241 others(8): Show |
11 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-6576T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965592 | |||||||
| chr13:40965635 | A | AT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0254 a0001c0001t0001g0255 others(8): Show |
13 | HG02071.hp1 HG02132.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-6620_73-6619ins others(1): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965635 | |||||||
| chr13:40965637 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(87): Show |
92 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.73-6621T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965637 | |||||||
| chr13:40965681 | A | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
58 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.73-6665T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965681 | |||||||
| chr13:40965792 | G | C | 1 | a0002c0002t0002g0024 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.73-6776C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965792 | |||||||
| chr13:40965836 | C | T | 1 | a0001c0003t0001g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.73-6820G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965836 | |||||||
| chr13:40965901 | A | G | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-6885T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965901 | |||||||
| chr13:40965981 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0305 |
3 | HG02056.hp1 NA18999.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.73-6965G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40965981 | |||||||
| chr13:40966228 | A | C | 1 | a0001c0001t0001g0249 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.73-7212T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966228 | |||||||
| chr13:40966366 | A | T | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-7350T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966366 | |||||||
| chr13:40966429 | G | GA | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-7414dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966429 | |||||||
| chr13:40966493 | G | A | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-7477C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966493 | |||||||
| chr13:40966532 | C | T | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-7516G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966532 | |||||||
| chr13:40966642 | C | T | 1 | a0001c0005t0003g0338 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.73-7626G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966642 | |||||||
| chr13:40966733 | C | G | 1 | a0001c0001t0001g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.73-7717G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966733 | |||||||
| chr13:40966902 | T | C | 11 | a0001c0001t0015g0011 a0001c0005t0003g0101 a0001c0005t0003g0241 others(8): Show |
11 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-7886A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966902 | |||||||
| chr13:40966931 | A | G | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-7915T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40966931 | |||||||
| chr13:40967194 | A | G | 7 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0267 others(4): Show |
7 | HG00609.hp1 HG01934.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-8178T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967194 | |||||||
| chr13:40967215 | T | C | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-8199A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967215 | |||||||
| chr13:40967244 | C | T | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.73-8228G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967244 | |||||||
| chr13:40967383 | T | A | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-8367A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967383 | |||||||
| chr13:40967522 | A | G | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-8506T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967522 | |||||||
| chr13:40967524 | T | C | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-8508A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967524 | |||||||
| chr13:40967695 | A | T | 1 | a0002c0002t0002g0034 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.73-8679T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967695 | |||||||
| chr13:40967712 | C | T | 1 | a0008c0017t0004g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.73-8696G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967712 | |||||||
| chr13:40967737 | G | A | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-8721C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967737 | |||||||
| chr13:40967758 | AT | A | 11 | a0001c0001t0015g0011 a0001c0005t0003g0101 a0001c0005t0003g0241 others(8): Show |
11 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.73-8743delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967758 | |||||||
| chr13:40967828 | C | T | 2 | a0001c0001t0001g0314 a0001c0001t0001g0316 |
2 | NA18954.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.73-8812G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967828 | |||||||
| chr13:40967845 | G | A | 5 | a0001c0001t0014g0283 a0001c0003t0001g0078 a0001c0003t0001g0251 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-8829C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967845 | |||||||
| chr13:40967878 | C | T | 73 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(70): Show |
74 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.73-8862G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40967878 | |||||||
| chr13:40968084 | T | C | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9068A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968084 | |||||||
| chr13:40968144 | A | G | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9128T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968144 | |||||||
| chr13:40968286 | G | A | 1 | a0001c0003t0001g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.73-9270C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968286 | |||||||
| chr13:40968335 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.73-9319C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968335 | |||||||
| chr13:40968496 | T | C | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9480A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968496 | |||||||
| chr13:40968533 | T | G | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.73-9517A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968533 | |||||||
| chr13:40968545 | G | A | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9529C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968545 | |||||||
| chr13:40968572 | A | G | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9556T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968572 | |||||||
| chr13:40968654 | T | C | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-9638A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968654 | |||||||
| chr13:40968702 | T | C | 1 | a0011c0011t0001g0274 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.73-9686A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968702 | |||||||
| chr13:40968721 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-9717_73-9706dup others(12): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968721 | |||||||
| chr13:40968721 | CT | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0137 a0001c0001t0001g0147 others(4): Show |
7 | HG00609.hp1 NA18942.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-9706delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968721 | |||||||
| chr13:40968740 | G | A | 6 | a0001c0001t0001g0237 a0001c0001t0001g0246 a0001c0001t0001g0248 others(3): Show |
6 | NA18939.hp1 NA18962.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-9724C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968740 | |||||||
| chr13:40968911 | G | A | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.73-9895C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40968911 | |||||||
| chr13:40969020 | A | T | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-10004T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969020 | |||||||
| chr13:40969152 | G | A | 3 | a0001c0001t0001g0115 a0001c0001t0001g0288 a0001c0001t0001g0304 |
3 | NA18941.hp1 NA19065.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.73-10136C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969152 | |||||||
| chr13:40969228 | T | C | 2 | a0001c0001t0001g0288 a0001c0001t0001g0304 |
2 | NA18941.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.73-10212A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969228 | |||||||
| chr13:40969358 | T | C | 109 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0017 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.73-10342A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969358 | |||||||
| chr13:40969567 | T | C | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.73-10551A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969567 | |||||||
| chr13:40969693 | A | G | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-10677T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969693 | |||||||
| chr13:40969766 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.73-10750G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969766 | |||||||
| chr13:40969878 | A | AT | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.73-10863dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969878 | |||||||
| chr13:40969962 | A | T | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-10946T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969962 | |||||||
| chr13:40969967 | T | A | 1 | a0002c0002t0002g0037 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.73-10951A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40969967 | |||||||
| chr13:40970197 | G | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0134 others(3): Show |
8 | NA18942.hp2 NA18952.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-11181C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970197 | |||||||
| chr13:40970248 | C | G | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.73-11232G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970248 | |||||||
| chr13:40970298 | T | C | 1 | a0001c0003t0001g0172 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-11282A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970298 | |||||||
| chr13:40970365 | TA | T | 8 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0002g0045 others(5): Show |
8 | HG00733.hp2 HG00738.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-11350delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970365 | |||||||
| chr13:40970424 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(83): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.73-11408G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970424 | |||||||
| chr13:40970430 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0015g0011 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.73-11414T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970430 | |||||||
| chr13:40970516 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0015g0011 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+11467A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970516 | |||||||
| chr13:40970587 | G | C | 12 | a0001c0001t0001g0038 a0001c0001t0015g0011 a0001c0005t0003g0101 others(9): Show |
12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+11396C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970587 | |||||||
| chr13:40970616 | C | T | 3 | a0006c0008t0006g0160 a0006c0008t0006g0161 a0010c0009t0006g0296 |
3 | HG02572.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.72+11367G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970616 | |||||||
| chr13:40970698 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0015g0011 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+11285C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970698 | |||||||
| chr13:40970929 | G | A | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.72+11054C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970929 | |||||||
| chr13:40970936 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0015g0011 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+11047G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40970936 | |||||||
| chr13:40971109 | TATAG | T | 8 | a0002c0002t0002g0043 a0002c0002t0002g0044 a0002c0002t0002g0045 others(5): Show |
8 | HG00733.hp2 HG00738.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+10870_72+10873d others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971109 | |||||||
| chr13:40971152 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0015g0011 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+10831C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971152 | |||||||
| chr13:40971172 | T | G | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+10811A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971172 | |||||||
| chr13:40971343 | C | G | 3 | a0006c0008t0006g0160 a0006c0008t0006g0161 a0010c0009t0006g0296 |
3 | HG02572.hp2 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.72+10640G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971343 | |||||||
| chr13:40971352 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+10631C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971352 | |||||||
| chr13:40971371 | A | C | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.72+10612T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971371 | |||||||
| chr13:40971433 | T | G | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+10550A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971433 | |||||||
| chr13:40971651 | A | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+10332T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971651 | |||||||
| chr13:40971949 | T | TG | 12 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(9): Show |
12 | HG00408.hp1 HG03654.hp2 HG04204.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+10033_72+10034i others(3): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971949 | |||||||
| chr13:40971950 | T | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(84): Show |
89 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.72+10033A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971950 | |||||||
| chr13:40971950 | TG | T | 117 | a0001c0001t0001g0207 a0001c0001t0001g0309 a0002c0002t0002g0003 others(114): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.72+10032delC | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971950 | |||||||
| chr13:40971951 | G | T | 1 | a0001c0001t0005g0093 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.72+10032C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971951 | |||||||
| chr13:40971959 | G | T | 1 | a0001c0005t0003g0341 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.72+10024C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40971959 | |||||||
| chr13:40972135 | T | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+9848A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972135 | |||||||
| chr13:40972252 | T | C | 4 | a0001c0003t0001g0154 a0001c0003t0001g0155 a0001c0003t0001g0170 others(1): Show |
4 | NA18940.hp2 NA19054.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+9731A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972252 | |||||||
| chr13:40972301 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0246 |
2 | HG01981.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.72+9682G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972301 | |||||||
| chr13:40972320 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.72+9663C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972320 | |||||||
| chr13:40972434 | T | C | 2 | a0002c0002t0002g0048 a0002c0002t0002g0049 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.72+9549A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972434 | |||||||
| chr13:40972502 | G | A | 3 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0328 |
3 | HG02622.hp1 HG02897.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.72+9481C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972502 | |||||||
| chr13:40972577 | T | C | 2 | a0001c0001t0001g0263 a0001c0001t0001g0277 |
2 | HG03654.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.72+9406A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972577 | |||||||
| chr13:40972578 | A | G | 74 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(71): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.72+9405T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972578 | |||||||
| chr13:40972831 | T | G | 1 | a0001c0003t0001g0171 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.72+9152A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972831 | |||||||
| chr13:40972905 | T | G | 6 | a0001c0001t0001g0237 a0001c0001t0001g0246 a0001c0001t0001g0248 others(3): Show |
6 | NA18939.hp1 NA18962.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+9078A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40972905 | |||||||
| chr13:40973007 | T | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(42): Show |
48 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.72+8976A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973007 | |||||||
| chr13:40973014 | C | G | 1 | a0001c0003t0001g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.72+8969G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973014 | |||||||
| chr13:40973016 | G | C | 1 | a0002c0002t0002g0022 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.72+8967C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973016 | |||||||
| chr13:40973147 | G | C | 2 | a0001c0001t0001g0038 a0001c0001t0015g0011 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+8836C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973147 | |||||||
| chr13:40973221 | C | T | 4 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0094 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+8762G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973221 | |||||||
| chr13:40973520 | T | C | 2 | a0001c0001t0001g0038 a0001c0001t0015g0011 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.72+8463A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973520 | |||||||
| chr13:40973572 | C | T | 1 | a0001c0003t0001g0153 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.72+8411G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973572 | |||||||
| chr13:40973642 | C | CT | 10 | a0001c0001t0001g0062 a0001c0001t0001g0278 a0001c0001t0014g0283 others(7): Show |
10 | HG01070.hp1 HG01071.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+8340dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973642 | |||||||
| chr13:40973642 | CT | C | 12 | a0001c0001t0001g0073 a0001c0001t0015g0011 a0001c0005t0003g0101 others(9): Show |
12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+8340delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40973642 | |||||||
| chr13:40974022 | G | C | 1 | a0001c0005t0003g0336 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.72+7961C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40974022 | |||||||
| chr13:40974195 | GT | G | 108 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(105): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.72+7787delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40974195 | |||||||
| chr13:40974204 | A | T | 8 | a0001c0001t0001g0264 a0001c0001t0001g0301 a0001c0001t0001g0302 others(5): Show |
8 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+7779T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40974204 | |||||||
| chr13:40974256 | T | TACTA | 12 | a0001c0001t0001g0038 a0001c0001t0015g0011 a0001c0005t0003g0101 others(9): Show |
12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+7723_72+7726dup others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40974256 | |||||||
| chr13:40974368 | T | C | 12 | a0001c0001t0001g0038 a0001c0001t0015g0011 a0001c0005t0003g0101 others(9): Show |
12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+7615A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40974368 | |||||||
| chr13:40975137 | C | T | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(345): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.72+6846G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975137 | |||||||
| chr13:40975187 | G | A | 1 | a0001c0001t0005g0095 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.72+6796C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975187 | |||||||
| chr13:40975226 | T | C | 1 | a0002c0002t0002g0191 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.72+6757A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975226 | |||||||
| chr13:40975380 | G | T | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.72+6603C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975380 | |||||||
| chr13:40975423 | G | C | 8 | a0004c0006t0004g0010 a0004c0006t0004g0012 a0004c0006t0004g0177 others(5): Show |
8 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+6560C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975423 | |||||||
| chr13:40975481 | C | A | 2 | a0003c0004t0001g0192 a0003c0004t0001g0198 |
2 | HG00423.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.72+6502G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975481 | |||||||
| chr13:40975804 | GGTAA | G | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+6175_72+6178del others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40975804 | |||||||
| chr13:40976173 | G | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0179 |
3 | NA18993.hp1 NA18994.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.72+5810C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976173 | |||||||
| chr13:40976306 | A | G | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.72+5677T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976306 | |||||||
| chr13:40976333 | A | G | 1 | a0001c0001t0001g0346 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.72+5650T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976333 | |||||||
| chr13:40976379 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.72+5604G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976379 | |||||||
| chr13:40976519 | G | C | 4 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0094 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+5464C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976519 | |||||||
| chr13:40976778 | GAT | G | 12 | a0001c0001t0001g0038 a0001c0001t0015g0011 a0001c0005t0003g0101 others(9): Show |
12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+5203_72+5204del others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976778 | |||||||
| chr13:40976789 | C | T | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+5194G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976789 | |||||||
| chr13:40976791 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.72+5192G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976791 | |||||||
| chr13:40976792 | G | A | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+5191C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976792 | |||||||
| chr13:40976832 | A | G | 2 | a0001c0001t0008g0143 a0001c0001t0008g0284 |
2 | HG02145.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.72+5151T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976832 | |||||||
| chr13:40976859 | C | A | 1 | a0001c0003t0001g0159 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.72+5124G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976859 | |||||||
| chr13:40976998 | CT | C | 12 | a0001c0001t0001g0038 a0001c0001t0015g0011 a0001c0005t0003g0101 others(9): Show |
12 | HG02559.hp1 HG03834.hp2 NA18612.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+4984delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40976998 | |||||||
| chr13:40977024 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.72+4959G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977024 | |||||||
| chr13:40977132 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.72+4851C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977132 | |||||||
| chr13:40977203 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.72+4780G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977203 | |||||||
| chr13:40977219 | G | A | 4 | a0001c0005t0003g0336 a0001c0005t0003g0338 a0001c0005t0003g0339 others(1): Show |
4 | NA18950.hp1 NA18986.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+4764C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977219 | |||||||
| chr13:40977468 | T | C | 75 | a0001c0001t0001g0038 a0001c0001t0001g0064 a0001c0001t0001g0065 others(72): Show |
76 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.72+4515A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977468 | |||||||
| chr13:40977890 | A | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+4093T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977890 | |||||||
| chr13:40977893 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.72+4090G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40977893 | |||||||
| chr13:40978070 | CAT | C | 8 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
8 | NA18959.hp1 NA18977.hp2 NA18997.hp2 others(5): Show |
intron_variant | MODIFIER | c.72+3911_72+3912del others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978070 | |||||||
| chr13:40978101 | C | T | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+3882G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978101 | |||||||
| chr13:40978377 | C | CA | 75 | a0001c0001t0001g0001 a0001c0001t0001g0040 a0001c0001t0001g0058 others(72): Show |
77 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.72+3605dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978377 | |||||||
| chr13:40978387 | A | AC | 12 | a0001c0001t0001g0013 a0001c0001t0001g0085 a0001c0001t0001g0086 others(9): Show |
12 | HG00408.hp1 NA18942.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+3595dupG | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978387 | |||||||
| chr13:40978401 | A | G | 4 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0094 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+3582T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978401 | |||||||
| chr13:40978404 | A | C | 8 | a0001c0001t0001g0264 a0001c0001t0001g0301 a0001c0001t0001g0302 others(5): Show |
8 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+3579T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978404 | |||||||
| chr13:40978560 | G | C | 1 | a0001c0005t0003g0337 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.72+3423C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978560 | |||||||
| chr13:40978593 | G | A | 111 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0207 others(108): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.72+3390C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978593 | |||||||
| chr13:40978602 | G | A | 292 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(289): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.72+3381C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978602 | |||||||
| chr13:40978652 | C | T | 7 | a0001c0001t0001g0038 a0001c0001t0014g0283 a0001c0001t0015g0011 others(4): Show |
7 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.72+3331G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978652 | |||||||
| chr13:40978781 | T | G | 4 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0094 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+3202A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978781 | |||||||
| chr13:40978903 | G | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(84): Show |
89 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.72+3080C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40978903 | |||||||
| chr13:40979011 | ATAGT | A | 69 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(66): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.72+2968_72+2971del others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979011 | |||||||
| chr13:40979012 | T | C | 6 | a0001c0001t0001g0239 a0001c0001t0001g0267 a0001c0001t0001g0268 others(3): Show |
6 | HG00609.hp1 NA18952.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+2971A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979012 | |||||||
| chr13:40979088 | A | C | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.72+2895T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979088 | |||||||
| chr13:40979165 | TTC | T | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+2816_72+2817del others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979165 | |||||||
| chr13:40979218 | T | TAC | 22 | a0001c0001t0001g0038 a0001c0001t0001g0115 a0001c0001t0001g0140 others(19): Show |
22 | HG00673.hp1 HG02135.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.72+2763_72+2764dup others(2): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979218 | |||||||
| chr13:40979218 | T | TACAC | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(213): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.72+2761_72+2764dup others(4): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979218 | |||||||
| chr13:40979218 | T | TACACAC | 108 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(105): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.72+2759_72+2764dup others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979218 | |||||||
| chr13:40979234 | T | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0115 a0001c0001t0001g0140 others(9): Show |
12 | HG00673.hp1 HG02135.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.72+2749A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979234 | |||||||
| chr13:40979271 | T | C | 1 | a0001c0001t0001g0264 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.72+2712A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979271 | |||||||
| chr13:40979424 | A | G | 1 | a0002c0002t0002g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.72+2559T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979424 | |||||||
| chr13:40979435 | C | T | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+2548G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979435 | |||||||
| chr13:40979678 | G | C | 1 | a0001c0001t0001g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.72+2305C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979678 | |||||||
| chr13:40979768 | G | A | 38 | a0001c0001t0001g0013 a0001c0001t0001g0058 a0001c0001t0001g0077 others(35): Show |
38 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.72+2215C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40979768 | |||||||
| chr13:40980145 | C | T | 1 | a0002c0002t0002g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.72+1838G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40980145 | |||||||
| chr13:40980495 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0002g0111 |
2 | HG02109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.72+1488T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40980495 | |||||||
| chr13:40980557 | T | C | 109 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.72+1426A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40980557 | |||||||
| chr13:40980839 | A | G | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.72+1144T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40980839 | |||||||
| chr13:40981110 | TTA | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(103): Show |
108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+871_72+872delTA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981110 | |||||||
| chr13:40981216 | C | A | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.72+767G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981216 | |||||||
| chr13:40981265 | T | C | 6 | a0001c0001t0014g0283 a0001c0001t0015g0011 a0001c0003t0001g0078 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+718A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981265 | |||||||
| chr13:40981588 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.72+395C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981588 | |||||||
| chr13:40981609 | TGAA | T | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+371_72+373delTT others(1): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981609 | |||||||
| chr13:40981665 | A | C | 1 | a0002c0002t0002g0205 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.72+318T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981665 | |||||||
| chr13:40981862 | T | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+121A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 2/8 | chr13 | 40981862 | |||||||
| chr13:40982457 | C | G | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-228-175G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982457 | |||||||
| chr13:40982550 | TA | T | 87 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-228-269delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982550 | |||||||
| chr13:40982681 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-228-399T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982681 | |||||||
| chr13:40982763 | G | C | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-228-481C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982763 | |||||||
| chr13:40982921 | T | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-228-639A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982921 | |||||||
| chr13:40982954 | CT | C | 14 | a0002c0002t0002g0019 a0002c0002t0002g0021 a0002c0002t0002g0074 others(11): Show |
14 | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.-228-673delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982954 | |||||||
| chr13:40982982 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(41): Show |
47 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.-228-700A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40982982 | |||||||
| chr13:40983088 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-228-806C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983088 | |||||||
| chr13:40983187 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0229 |
3 | HG00639.hp1 HG03239.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-228-905G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983187 | |||||||
| chr13:40983640 | T | G | 4 | a0001c0003t0001g0173 a0001c0003t0001g0174 a0001c0003t0001g0312 others(1): Show |
4 | NA18612.hp2 NA18946.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-228-1358A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983640 | |||||||
| chr13:40983689 | G | GA | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-1408dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983689 | |||||||
| chr13:40983817 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0285 |
2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-228-1535T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983817 | |||||||
| chr13:40983841 | G | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-228-1559C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983841 | |||||||
| chr13:40983861 | TTC | T | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-1581_-228-158 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983861 | |||||||
| chr13:40983914 | A | G | 3 | a0001c0003t0001g0007 a0001c0003t0001g0153 a0001c0003t0001g0159 |
4 | HG00741.hp2 HG01346.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-228-1632T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983914 | |||||||
| chr13:40983974 | A | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-228-1692T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40983974 | |||||||
| chr13:40984095 | T | A | 8 | a0004c0006t0004g0010 a0004c0006t0004g0012 a0004c0006t0004g0177 others(5): Show |
8 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-228-1813A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984095 | |||||||
| chr13:40984163 | C | A | 1 | a0001c0003t0001g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-228-1881G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984163 | |||||||
| chr13:40984223 | C | T | 4 | a0002c0002t0002g0051 a0002c0002t0002g0052 a0002c0002t0002g0053 others(1): Show |
4 | HG01071.hp2 HG02293.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-228-1941G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984223 | |||||||
| chr13:40984226 | C | T | 3 | a0002c0002t0002g0220 a0002c0002t0002g0222 a0002c0002t0002g0223 |
3 | HG01934.hp1 HG02040.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-228-1944G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984226 | |||||||
| chr13:40984278 | A | C | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-1996T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984278 | |||||||
| chr13:40984360 | T | C | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-2078A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984360 | |||||||
| chr13:40984492 | C | T | 2 | a0002c0002t0002g0185 a0003c0004t0001g0193 |
2 | NA18957.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-228-2210G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984492 | |||||||
| chr13:40984513 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-228-2231T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984513 | |||||||
| chr13:40984637 | A | G | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-228-2355T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984637 | |||||||
| chr13:40984939 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-228-2657A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984939 | |||||||
| chr13:40984952 | C | T | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-228-2670G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40984952 | |||||||
| chr13:40985840 | T | C | 2 | a0001c0001t0001g0297 a0001c0001t0001g0345 |
2 | HG00544.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-228-3558A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40985840 | |||||||
| chr13:40986018 | TA | T | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-228-3737delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986018 | |||||||
| chr13:40986103 | C | T | 4 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0094 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-228-3821G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986103 | |||||||
| chr13:40986176 | A | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(103): Show |
108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-228-3894T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986176 | |||||||
| chr13:40986294 | T | A | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-4012A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986294 | |||||||
| chr13:40986466 | C | T | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-4184G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986466 | |||||||
| chr13:40986567 | T | C | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-4285A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986567 | |||||||
| chr13:40986642 | C | T | 1 | a0001c0001t0011g0326 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-228-4360G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986642 | |||||||
| chr13:40986653 | C | CTCTG | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-228-4375_-228-437 others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986653 | |||||||
| chr13:40986718 | T | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-4436A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986718 | |||||||
| chr13:40986726 | A | G | 6 | a0001c0001t0001g0239 a0001c0001t0001g0267 a0001c0001t0001g0268 others(3): Show |
6 | HG00609.hp1 NA18952.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.-228-4444T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986726 | |||||||
| chr13:40986766 | CA | C | 7 | a0001c0001t0001g0038 a0001c0001t0014g0283 a0001c0001t0015g0011 others(4): Show |
7 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-228-4485delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986766 | |||||||
| chr13:40986786 | T | A | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-228-4504A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986786 | |||||||
| chr13:40986937 | C | CTCT | 9 | a0001c0001t0001g0038 a0001c0001t0014g0283 a0001c0001t0015g0011 others(6): Show |
9 | HG01168.hp1 HG02145.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-228-4656_-228-465 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986937 | |||||||
| chr13:40986937 | C | CTCTT | 110 | a0001c0001t0001g0207 a0001c0001t0001g0299 a0002c0002t0002g0003 others(107): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-228-4656_-228-465 others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986937 | |||||||
| chr13:40986937 | C | CTCTTT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(91): Show |
96 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-228-4656_-228-465 others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986937 | |||||||
| chr13:40986937 | C | CTCTTTT | 61 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(58): Show |
66 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(63): Show |
intron_variant | MODIFIER | c.-228-4656_-228-465 others(10): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986937 | |||||||
| chr13:40986937 | C | CTTT | 68 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(65): Show |
69 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.-228-4658_-228-465 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40986937 | |||||||
| chr13:40987004 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-228-4722G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987004 | |||||||
| chr13:40987081 | G | A | 1 | a0002c0002t0002g0032 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-228-4799C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987081 | |||||||
| chr13:40987093 | G | T | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-4811C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987093 | |||||||
| chr13:40987096 | C | T | 2 | a0002c0002t0002g0053 a0004c0006t0004g0012 |
2 | HG02723.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-228-4814G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987096 | |||||||
| chr13:40987102 | A | T | 1 | a0002c0002t0002g0053 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-228-4820T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987102 | |||||||
| chr13:40987299 | T | C | 1 | a0004c0006t0004g0333 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-228-5017A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987299 | |||||||
| chr13:40987402 | G | A | 4 | a0001c0005t0003g0336 a0001c0005t0003g0338 a0001c0005t0003g0339 others(1): Show |
4 | NA18950.hp1 NA18986.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.-228-5120C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987402 | |||||||
| chr13:40987428 | A | C | 19 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(16): Show |
19 | HG00423.hp1 HG01192.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.-228-5146T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987428 | |||||||
| chr13:40987428 | A | G | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-228-5146T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987428 | |||||||
| chr13:40987537 | G | T | 6 | a0001c0001t0014g0283 a0001c0001t0015g0011 a0001c0003t0001g0078 others(3): Show |
6 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-228-5255C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987537 | |||||||
| chr13:40987584 | C | CA | 147 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(144): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-228-5303dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987584 | |||||||
| chr13:40987584 | C | CAA | 25 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(22): Show |
25 | HG00408.hp2 HG00544.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-228-5304_-228-530 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987584 | |||||||
| chr13:40987584 | CA | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(43): Show |
51 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.-228-5303delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987584 | |||||||
| chr13:40987600 | A | AAG | 7 | a0002c0002t0002g0034 a0002c0002t0002g0048 a0002c0002t0002g0049 others(4): Show |
7 | HG00673.hp2 HG02717.hp2 NA18998.hp2 others(4): Show |
intron_variant | MODIFIER | c.-228-5319_-228-531 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987600 | |||||||
| chr13:40987600 | A | AG | 99 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(96): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.-228-5319_-228-531 others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987600 | |||||||
| chr13:40987600 | A | G | 3 | a0002c0002t0002g0191 a0003c0004t0001g0225 a0003c0016t0001g0057 |
3 | HG02965.hp1 NA18953.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-228-5318T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987600 | |||||||
| chr13:40987757 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-228-5475A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987757 | |||||||
| chr13:40987827 | TAA | T | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-5547_-228-554 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987827 | |||||||
| chr13:40987832 | G | A | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-5550C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987832 | |||||||
| chr13:40987833 | A | G | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-5551T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987833 | |||||||
| chr13:40987922 | G | A | 1 | a0004c0006t0004g0334 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-228-5640C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40987922 | |||||||
| chr13:40988121 | A | G | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-5839T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988121 | |||||||
| chr13:40988191 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-228-5909G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988191 | |||||||
| chr13:40988297 | G | C | 4 | a0001c0001t0001g0314 a0001c0001t0001g0316 a0001c0001t0001g0320 others(1): Show |
4 | NA18954.hp2 NA18986.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-228-6015C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988297 | |||||||
| chr13:40988393 | C | T | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-228-6111G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988393 | |||||||
| chr13:40988650 | A | G | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-6368T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988650 | |||||||
| chr13:40988724 | C | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-228-6442G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988724 | |||||||
| chr13:40988846 | G | C | 1 | a0002c0002t0002g0035 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-228-6564C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988846 | |||||||
| chr13:40988883 | C | T | 109 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-6601G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988883 | |||||||
| chr13:40988890 | T | C | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-228-6608A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40988890 | |||||||
| chr13:40989015 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(103): Show |
108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-228-6733G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989015 | |||||||
| chr13:40989150 | C | T | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-6868G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989150 | |||||||
| chr13:40989237 | A | G | 1 | a0001c0001t0013g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-228-6955T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989237 | |||||||
| chr13:40989248 | G | A | 1 | a0002c0002t0002g0039 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-228-6966C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989248 | |||||||
| chr13:40989284 | A | G | 1 | a0002c0002t0002g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-228-7002T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989284 | |||||||
| chr13:40989452 | T | C | 109 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-7170A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989452 | |||||||
| chr13:40989626 | CT | C | 109 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-7345delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989626 | |||||||
| chr13:40989634 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-228-7352G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989634 | |||||||
| chr13:40989766 | T | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-228-7484A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989766 | |||||||
| chr13:40989767 | G | C | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-228-7485C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989767 | |||||||
| chr13:40989994 | A | C | 1 | a0001c0003t0001g0324 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-228-7712T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40989994 | |||||||
| chr13:40990003 | C | T | 109 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-7721G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990003 | |||||||
| chr13:40990017 | A | AAT | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-7737_-228-773 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990017 | |||||||
| chr13:40990039 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-228-7757T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990039 | |||||||
| chr13:40990151 | A | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-228-7869T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990151 | |||||||
| chr13:40990286 | G | A | 69 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(66): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-228-8004C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990286 | |||||||
| chr13:40990387 | A | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0158 |
2 | HG02698.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-228-8105T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990387 | |||||||
| chr13:40990448 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0270 |
2 | NA18985.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-228-8166A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990448 | |||||||
| chr13:40990545 | A | G | 1 | a0004c0006t0004g0177 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-228-8263T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990545 | |||||||
| chr13:40990837 | C | T | 109 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-8555G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990837 | |||||||
| chr13:40990850 | C | CA | 138 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(135): Show |
142 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-228-8569dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990850 | |||||||
| chr13:40990850 | C | CAA | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.-228-8570_-228-856 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990850 | |||||||
| chr13:40990850 | C | CAAA | 6 | a0001c0001t0001g0149 a0001c0003t0001g0175 a0001c0003t0001g0282 others(3): Show |
6 | HG02135.hp2 HG02293.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-228-8571_-228-856 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990850 | |||||||
| chr13:40990850 | CA | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-8569delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990850 | |||||||
| chr13:40990885 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-228-8603A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990885 | |||||||
| chr13:40990904 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-228-8622G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40990904 | |||||||
| chr13:40991204 | T | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0285 |
2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-228-8922A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991204 | |||||||
| chr13:40991204 | T | C | 109 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-8922A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991204 | |||||||
| chr13:40991252 | C | G | 1 | a0002c0002t0002g0034 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-228-8970G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991252 | |||||||
| chr13:40991567 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-228-9285T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991567 | |||||||
| chr13:40991577 | C | T | 8 | a0001c0001t0001g0264 a0001c0001t0001g0301 a0001c0001t0001g0302 others(5): Show |
8 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-228-9295G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991577 | |||||||
| chr13:40991582 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(88): Show |
93 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.-228-9300G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991582 | |||||||
| chr13:40991678 | T | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-9396A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991678 | |||||||
| chr13:40991967 | G | T | 1 | a0001c0001t0001g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-228-9685C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40991967 | |||||||
| chr13:40992013 | GA | G | 4 | a0001c0003t0001g0156 a0001c0003t0001g0157 a0001c0003t0001g0176 others(1): Show |
4 | HG00597.hp2 NA18948.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.-228-9732delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992013 | |||||||
| chr13:40992021 | T | C | 5 | a0001c0001t0014g0283 a0001c0003t0001g0078 a0001c0003t0001g0251 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-228-9739A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992021 | |||||||
| chr13:40992380 | G | C | 1 | a0002c0002t0002g0056 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-228-10098C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992380 | |||||||
| chr13:40992401 | T | C | 1 | a0002c0002t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-228-10119A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992401 | |||||||
| chr13:40992431 | T | C | 1 | a0001c0003t0001g0282 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-228-10149A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992431 | |||||||
| chr13:40992629 | T | TA | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-10348_-228-10 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992629 | |||||||
| chr13:40992641 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-228-10359G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992641 | |||||||
| chr13:40992645 | G | A | 111 | a0001c0001t0001g0207 a0001c0001t0001g0267 a0001c0001t0001g0293 others(108): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-228-10363C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40992645 | |||||||
| chr13:40993112 | C | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(102): Show |
107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-228-10830G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993112 | |||||||
| chr13:40993394 | G | T | 15 | a0001c0001t0001g0038 a0001c0001t0014g0283 a0001c0001t0015g0011 others(12): Show |
15 | HG01192.hp2 HG01496.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-228-11112C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993394 | |||||||
| chr13:40993428 | C | A | 110 | a0001c0001t0001g0207 a0001c0001t0001g0267 a0002c0002t0002g0003 others(107): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-228-11146G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993428 | |||||||
| chr13:40993473 | C | T | 1 | a0001c0005t0003g0336 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-228-11191G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993473 | |||||||
| chr13:40993517 | G | A | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-11235C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993517 | |||||||
| chr13:40993521 | C | T | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-11239G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993521 | |||||||
| chr13:40993899 | A | AT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(83): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-228-11618dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40993899 | |||||||
| chr13:40994009 | T | TA | 9 | a0002c0002t0002g0024 a0002c0002t0002g0043 a0002c0002t0002g0044 others(6): Show |
9 | HG00733.hp2 HG00738.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.-228-11728dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994009 | |||||||
| chr13:40994009 | T | TG | 11 | a0001c0001t0001g0145 a0001c0005t0003g0101 a0001c0005t0003g0241 others(8): Show |
11 | HG02027.hp2 HG03834.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.-228-11728_-228-11 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994009 | |||||||
| chr13:40994010 | A | G | 70 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(67): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-228-11728T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994010 | |||||||
| chr13:40994179 | T | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-11897A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994179 | |||||||
| chr13:40994505 | T | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(102): Show |
107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-228-12223A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994505 | |||||||
| chr13:40994656 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-228-12374A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994656 | |||||||
| chr13:40994736 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-228-12454C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40994736 | |||||||
| chr13:40995072 | G | A | 1 | a0002c0002t0002g0004 | 2 | HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-228-12790C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40995072 | |||||||
| chr13:40995662 | T | TA | 9 | a0001c0001t0001g0086 a0004c0006t0004g0010 a0004c0006t0004g0012 others(6): Show |
9 | HG01192.hp2 HG01496.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-228-13381dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40995662 | |||||||
| chr13:40995662 | TA | T | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-228-13381delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40995662 | |||||||
| chr13:40995998 | T | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-13716A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40995998 | |||||||
| chr13:40996121 | T | C | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-228-13839A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996121 | |||||||
| chr13:40996195 | T | TAGGAATT others(333): Show |
1 | a0001c0001t0001g0151 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-228-13914_-228-13 others(346): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996195 | |||||||
| chr13:40996372 | G | A | 1 | a0001c0003t0001g0127 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-228-14090C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996372 | |||||||
| chr13:40996442 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0139 |
2 | NA18951.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-228-14160T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996442 | |||||||
| chr13:40996621 | G | A | 1 | a0001c0005t0003g0340 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-228-14339C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996621 | |||||||
| chr13:40996668 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-228-14386C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996668 | |||||||
| chr13:40996780 | CT | C | 21 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(18): Show |
21 | HG00408.hp2 HG00544.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.-228-14499delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40996780 | |||||||
| chr13:40997089 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-228-14807G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997089 | |||||||
| chr13:40997257 | T | G | 1 | a0004c0006t0004g0331 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-228-14975A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997257 | |||||||
| chr13:40997407 | G | A | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-15125C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997407 | |||||||
| chr13:40997789 | T | G | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-15507A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997789 | |||||||
| chr13:40997824 | T | A | 1 | a0001c0001t0001g0285 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-228-15542A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997824 | |||||||
| chr13:40997891 | A | G | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-15609T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997891 | |||||||
| chr13:40997997 | A | T | 109 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-15715T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40997997 | |||||||
| chr13:40998038 | C | T | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-228-15756G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40998038 | |||||||
| chr13:40998053 | G | A | 2 | a0001c0001t0001g0147 a0005c0007t0001g0148 |
2 | HG02015.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-228-15771C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40998053 | |||||||
| chr13:40998197 | T | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-15915A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40998197 | |||||||
| chr13:40998731 | C | A | 1 | a0002c0002t0002g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-228-16449G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40998731 | |||||||
| chr13:40998967 | C | T | 1 | a0002c0002t0002g0221 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-228-16685G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40998967 | |||||||
| chr13:40999064 | C | T | 109 | a0001c0001t0001g0207 a0002c0002t0002g0003 a0002c0002t0002g0004 others(106): Show |
112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.-228-16782G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999064 | |||||||
| chr13:40999341 | G | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(103): Show |
108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-228-17059C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999341 | |||||||
| chr13:40999368 | TA | T | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-228-17087delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999368 | |||||||
| chr13:40999411 | G | A | 7 | a0001c0001t0001g0038 a0001c0001t0014g0283 a0001c0001t0015g0011 others(4): Show |
7 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-228-17129C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999411 | |||||||
| chr13:40999513 | T | A | 4 | a0002c0002t0002g0190 a0002c0002t0002g0201 a0002c0002t0002g0202 others(1): Show |
4 | NA18970.hp2 NA18978.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.-228-17231A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999513 | |||||||
| chr13:40999520 | T | G | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-17238A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999520 | |||||||
| chr13:40999565 | A | C | 15 | a0001c0001t0001g0038 a0001c0001t0014g0283 a0001c0001t0015g0011 others(12): Show |
15 | HG01192.hp2 HG01496.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-228-17283T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999565 | |||||||
| chr13:40999600 | T | G | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-17318A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999600 | |||||||
| chr13:40999672 | A | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-228-17390T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999672 | |||||||
| chr13:40999709 | C | T | 2 | a0002c0002t0002g0027 a0002c0002t0002g0028 |
2 | HG00735.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.-228-17427G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 40999709 | |||||||
| chr13:41000001 | T | C | 1 | a0002c0002t0002g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-228-17719A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000001 | |||||||
| chr13:41000160 | T | C | 7 | a0001c0001t0001g0038 a0001c0001t0014g0283 a0001c0001t0015g0011 others(4): Show |
7 | HG02145.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-228-17878A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000160 | |||||||
| chr13:41000237 | CT | C | 40 | a0001c0001t0001g0040 a0001c0001t0001g0058 a0001c0001t0001g0077 others(37): Show |
40 | HG00544.hp1 HG00621.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.-228-17956delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | |||||||
| chr13:41000237 | CTT | C | 98 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0038 others(95): Show |
100 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-228-17957_-228-17 others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | |||||||
| chr13:41000237 | CTTT | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
99 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.-228-17958_-228-17 others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | |||||||
| chr13:41000237 | CTTTT | C | 10 | a0002c0002t0002g0019 a0002c0002t0002g0021 a0002c0002t0002g0052 others(7): Show |
10 | HG01106.hp1 HG01109.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-17959_-228-17 others(10): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | |||||||
| chr13:41000237 | CTTTTTT | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0257 a0001c0001t0001g0258 others(5): Show |
10 | HG02132.hp1 HG02165.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.-228-17961_-228-17 others(12): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | |||||||
| chr13:41000237 | CTTTTTTT others(1): Show |
C | 67 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(64): Show |
68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.-228-17963_-228-17 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | |||||||
| chr13:41000237 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG02622.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-228-17966_-228-17 others(17): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | |||||||
| chr13:41000237 | CTTTTTTT others(7): Show |
C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-228-17969_-228-17 others(20): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000237 | |||||||
| chr13:41000382 | G | A | 1 | a0002c0002t0002g0036 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-228-18100C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000382 | |||||||
| chr13:41000464 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(84): Show |
89 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.-228-18182G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000464 | |||||||
| chr13:41000469 | G | GC | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-228-18188dupG | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000469 | |||||||
| chr13:41000500 | C | T | 1 | a0001c0003t0001g0324 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-228-18218G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000500 | |||||||
| chr13:41000505 | G | T | 1 | a0001c0003t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18223C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000505 | |||||||
| chr13:41000506 | C | A | 1 | a0001c0003t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18224G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000506 | |||||||
| chr13:41000509 | C | T | 1 | a0001c0003t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18227G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000509 | |||||||
| chr13:41000510 | C | A | 1 | a0001c0003t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18228G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000510 | |||||||
| chr13:41000511 | A | G | 1 | a0001c0003t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18229T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000511 | |||||||
| chr13:41000512 | C | T | 1 | a0001c0003t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18230G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000512 | |||||||
| chr13:41000513 | A | G | 1 | a0001c0003t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18231T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000513 | |||||||
| chr13:41000514 | C | A | 1 | a0001c0003t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18232G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000514 | |||||||
| chr13:41000517 | G | T | 1 | a0001c0003t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18235C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000517 | |||||||
| chr13:41000518 | G | T | 1 | a0001c0003t0001g0154 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-228-18236C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000518 | |||||||
| chr13:41000554 | T | G | 1 | a0002c0002t0002g0018 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-228-18272A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000554 | |||||||
| chr13:41000566 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-228-18284A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000566 | |||||||
| chr13:41000615 | G | A | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-18333C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000615 | |||||||
| chr13:41000627 | G | C | 1 | a0001c0003t0001g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-228-18345C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000627 | |||||||
| chr13:41000686 | G | A | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-228-18404C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000686 | |||||||
| chr13:41000861 | A | AAG | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-229+18365_-229+18 others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000861 | |||||||
| chr13:41000875 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-229+18353T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000875 | |||||||
| chr13:41000978 | C | CT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(101): Show |
106 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.-229+18249dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000978 | |||||||
| chr13:41000993 | C | G | 1 | a0001c0001t0001g0276 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-229+18235G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41000993 | |||||||
| chr13:41001139 | T | G | 82 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(79): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.-229+18089A>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001139 | |||||||
| chr13:41001255 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-229+17973C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001255 | |||||||
| chr13:41001287 | T | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(89): Show |
94 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.-229+17941A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001287 | |||||||
| chr13:41001409 | A | T | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-229+17819T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001409 | |||||||
| chr13:41001416 | C | T | 1 | a0001c0003t0001g0082 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-229+17812G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001416 | |||||||
| chr13:41001431 | T | A | 1 | a0001c0001t0001g0311 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-229+17797A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001431 | |||||||
| chr13:41001579 | A | C | 1 | a0001c0003t0001g0153 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-229+17649T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001579 | |||||||
| chr13:41001584 | G | A | 6 | a0002c0002t0002g0023 a0002c0002t0002g0037 a0002c0002t0002g0039 others(3): Show |
6 | NA18947.hp1 NA18948.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+17644C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001584 | |||||||
| chr13:41001588 | G | C | 1 | a0002c0002t0002g0107 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-229+17640C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001588 | |||||||
| chr13:41001651 | T | C | 1 | a0002c0002t0002g0351 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-229+17577A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001651 | |||||||
| chr13:41001668 | T | C | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-229+17560A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001668 | |||||||
| chr13:41001866 | C | T | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-229+17362G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41001866 | |||||||
| chr13:41002071 | C | T | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-229+17157G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002071 | |||||||
| chr13:41002111 | G | C | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-229+17117C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002111 | |||||||
| chr13:41002145 | G | A | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-229+17083C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002145 | |||||||
| chr13:41002186 | C | G | 71 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(68): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-229+17042G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002186 | |||||||
| chr13:41002246 | G | C | 1 | a0001c0001t0001g0306 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-229+16982C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002246 | |||||||
| chr13:41002262 | C | T | 3 | a0002c0002t0002g0220 a0002c0002t0002g0222 a0002c0002t0002g0223 |
3 | HG01934.hp1 HG02040.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-229+16966G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002262 | |||||||
| chr13:41002285 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0285 |
2 | HG01109.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-229+16943C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002285 | |||||||
| chr13:41002327 | T | A | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-229+16901A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002327 | |||||||
| chr13:41002333 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-229+16895T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002333 | |||||||
| chr13:41002410 | G | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-229+16818C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002410 | |||||||
| chr13:41002441 | G | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0038 others(103): Show |
108 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-229+16787C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002441 | |||||||
| chr13:41002584 | TA | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0005g0092 others(11): Show |
15 | HG01168.hp1 HG01192.hp2 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-229+16643delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002584 | |||||||
| chr13:41002759 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(83): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-229+16469C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41002759 | |||||||
| chr13:41003003 | C | G | 2 | a0001c0001t0001g0346 a0001c0001t0001g0347 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-229+16225G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003003 | |||||||
| chr13:41003028 | CT | C | 10 | a0001c0005t0003g0101 a0001c0005t0003g0241 a0001c0005t0003g0336 others(7): Show |
10 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.-229+16199delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003028 | |||||||
| chr13:41003035 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-229+16193A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003035 | |||||||
| chr13:41003054 | G | C | 3 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0001g0280 |
3 | NA18972.hp1 NA19011.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-229+16174C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003054 | |||||||
| chr13:41003070 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(83): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-229+16158A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003070 | |||||||
| chr13:41003171 | G | A | 1 | a0001c0001t0007g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-229+16057C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003171 | |||||||
| chr13:41003395 | AAATTAAA others(131): Show |
A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.-229+15695_-229+15 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003395 | |||||||
| chr13:41003539 | C | T | 1 | a0008c0017t0004g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-229+15689G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003539 | |||||||
| chr13:41003768 | G | A | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-229+15460C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003768 | |||||||
| chr13:41003973 | C | T | 81 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.-229+15255G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41003973 | |||||||
| chr13:41004063 | C | A | 10 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(7): Show |
10 | HG02717.hp2 NA18959.hp1 NA18977.hp2 others(7): Show |
intron_variant | MODIFIER | c.-229+15165G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41004063 | |||||||
| chr13:41004359 | G | A | 1 | a0002c0002t0002g0313 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-229+14869C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41004359 | |||||||
| chr13:41004596 | T | C | 1 | a0001c0005t0003g0340 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-229+14632A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41004596 | |||||||
| chr13:41004964 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-229+14264G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41004964 | |||||||
| chr13:41004977 | A | G | 43 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0018 others(40): Show |
45 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-229+14251T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41004977 | |||||||
| chr13:41005342 | G | A | 1 | a0001c0001t0008g0143 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-229+13886C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005342 | |||||||
| chr13:41005450 | C | CA | 128 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
134 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.-229+13777dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005450 | |||||||
| chr13:41005450 | C | CAA | 14 | a0001c0001t0001g0142 a0001c0001t0001g0290 a0001c0005t0003g0341 others(11): Show |
14 | HG01106.hp2 HG01934.hp1 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.-229+13776_-229+13 others(8): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005450 | |||||||
| chr13:41005466 | A | C | 1 | a0001c0001t0001g0150 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-229+13762T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005466 | |||||||
| chr13:41005673 | A | C | 90 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(87): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.-229+13555T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005673 | |||||||
| chr13:41005732 | T | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
59 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.-229+13496A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005732 | |||||||
| chr13:41005802 | G | A | 43 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0018 others(40): Show |
45 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-229+13426C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005802 | |||||||
| chr13:41005861 | T | C | 7 | a0004c0006t0004g0012 a0004c0006t0004g0177 a0004c0006t0004g0330 others(4): Show |
7 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+13367A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005861 | |||||||
| chr13:41005873 | A | ATCATAAA others(273): Show |
4 | a0002c0002t0002g0181 a0002c0002t0002g0221 a0002c0002t0002g0317 others(1): Show |
4 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-229+13075_-229+13 others(286): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41005873 | |||||||
| chr13:41006044 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0346 a0001c0001t0001g0347 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+13184A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006044 | |||||||
| chr13:41006076 | G | A | 1 | a0002c0002t0002g0351 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-229+13152C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006076 | |||||||
| chr13:41006123 | C | G | 43 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0018 others(40): Show |
45 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-229+13105G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006123 | |||||||
| chr13:41006219 | G | C | 1 | a0001c0001t0007g0344 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-229+13009C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006219 | |||||||
| chr13:41006324 | G | GT | 70 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(67): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-229+12903dupA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006324 | |||||||
| chr13:41006402 | C | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0138 a0001c0001t0001g0289 others(2): Show |
5 | NA18940.hp1 NA18963.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-229+12826G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006402 | |||||||
| chr13:41006407 | C | T | 1 | a0001c0003t0001g0072 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-229+12821G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006407 | |||||||
| chr13:41006442 | T | TG | 9 | a0001c0001t0007g0344 a0001c0005t0003g0336 a0001c0005t0003g0337 others(6): Show |
9 | HG03491.hp1 HG03834.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+12785dupC | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006442 | |||||||
| chr13:41006465 | T | C | 8 | a0001c0005t0003g0336 a0001c0005t0003g0337 a0001c0005t0003g0338 others(5): Show |
8 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.-229+12763A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006465 | |||||||
| chr13:41006769 | G | C | 2 | a0001c0001t0001g0320 a0001c0001t0001g0321 |
2 | NA18999.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-229+12459C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006769 | |||||||
| chr13:41006803 | G | A | 7 | a0004c0006t0004g0012 a0004c0006t0004g0177 a0004c0006t0004g0330 others(4): Show |
7 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+12425C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006803 | |||||||
| chr13:41006867 | C | T | 43 | a0002c0002t0002g0003 a0002c0002t0002g0004 a0002c0002t0002g0018 others(40): Show |
45 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-229+12361G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006867 | |||||||
| chr13:41006905 | A | G | 4 | a0001c0001t0005g0092 a0001c0001t0005g0093 a0001c0001t0005g0094 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-229+12323T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41006905 | |||||||
| chr13:41007001 | T | C | 7 | a0004c0006t0004g0012 a0004c0006t0004g0177 a0004c0006t0004g0330 others(4): Show |
7 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+12227A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41007001 | |||||||
| chr13:41007448 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-229+11780A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41007448 | |||||||
| chr13:41007530 | C | A | 90 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(87): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.-229+11698G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41007530 | |||||||
| chr13:41007794 | C | T | 90 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(87): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.-229+11434G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41007794 | |||||||
| chr13:41007847 | G | A | 5 | a0001c0001t0014g0283 a0001c0003t0001g0078 a0001c0003t0001g0251 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-229+11381C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41007847 | |||||||
| chr13:41008002 | C | G | 60 | a0001c0001t0001g0207 a0001c0001t0001g0218 a0001c0001t0001g0219 others(57): Show |
61 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-229+11226G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41008002 | |||||||
| chr13:41008139 | G | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(83): Show |
88 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.-229+11089C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41008139 | |||||||
| chr13:41008221 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0254 a0001c0001t0001g0255 others(8): Show |
13 | HG02071.hp1 HG02132.hp1 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.-229+11007G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41008221 | |||||||
| chr13:41008617 | G | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0309 a0001c0001t0001g0310 others(1): Show |
4 | HG03239.hp1 NA18957.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.-229+10611C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41008617 | |||||||
| chr13:41008969 | A | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(273): Show |
286 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-229+10259T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41008969 | |||||||
| chr13:41009181 | T | C | 1 | a0002c0002t0002g0055 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-229+10047A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41009181 | |||||||
| chr13:41009231 | T | C | 2 | a0002c0002t0002g0048 a0002c0002t0002g0049 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-229+9997A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41009231 | |||||||
| chr13:41009481 | T | C | 1 | a0001c0001t0013g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-229+9747A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41009481 | |||||||
| chr13:41009698 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-229+9530C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41009698 | |||||||
| chr13:41009805 | C | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(51): Show |
59 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.-229+9423G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41009805 | |||||||
| chr13:41010051 | GA | G | 69 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(66): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.-229+9176delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010051 | |||||||
| chr13:41010254 | T | C | 1 | a0001c0003t0001g0350 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-229+8974A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010254 | |||||||
| chr13:41010279 | GA | G | 87 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0065 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-229+8948delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010279 | |||||||
| chr13:41010313 | C | T | 9 | a0001c0001t0001g0062 a0001c0001t0007g0344 a0004c0006t0004g0012 others(6): Show |
9 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+8915G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010313 | |||||||
| chr13:41010338 | T | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(93): Show |
98 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-229+8890A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010338 | |||||||
| chr13:41010361 | G | A | 1 | a0001c0003t0001g0100 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-229+8867C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010361 | |||||||
| chr13:41010454 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-229+8774G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010454 | |||||||
| chr13:41010493 | A | ATG | 46 | a0001c0001t0001g0062 a0001c0001t0001g0253 a0001c0001t0001g0287 others(43): Show |
47 | HG00423.hp2 HG00673.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.-229+8733_-229+873 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010493 | |||||||
| chr13:41010512 | C | T | 7 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0029 others(4): Show |
7 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+8716G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010512 | |||||||
| chr13:41010513 | A | G | 7 | a0002c0002t0002g0027 a0002c0002t0002g0028 a0002c0002t0002g0029 others(4): Show |
7 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+8715T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010513 | |||||||
| chr13:41010554 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0040 others(176): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.-229+8674A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010554 | |||||||
| chr13:41010595 | T | C | 7 | a0004c0006t0004g0012 a0004c0006t0004g0177 a0004c0006t0004g0330 others(4): Show |
7 | HG01192.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+8633A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010595 | |||||||
| chr13:41010679 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-229+8549G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010679 | |||||||
| chr13:41010807 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-229+8421A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010807 | |||||||
| chr13:41010898 | G | C | 1 | a0002c0002t0002g0071 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-229+8330C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010898 | |||||||
| chr13:41010919 | T | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(14): Show |
20 | HG00438.hp2 HG00597.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.-229+8309A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41010919 | |||||||
| chr13:41011287 | T | C | 2 | a0002c0002t0002g0222 a0002c0002t0002g0223 |
2 | HG01934.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.-229+7941A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011287 | |||||||
| chr13:41011362 | A | T | 39 | a0001c0001t0001g0013 a0001c0001t0001g0077 a0001c0001t0001g0084 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.-229+7866T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011362 | |||||||
| chr13:41011507 | G | A | 1 | a0002c0002t0002g0041 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-229+7721C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011507 | |||||||
| chr13:41011590 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-229+7638G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011590 | |||||||
| chr13:41011644 | G | A | 74 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(71): Show |
75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.-229+7584C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011644 | |||||||
| chr13:41011778 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-229+7450C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011778 | |||||||
| chr13:41011887 | CT | C | 6 | a0004c0006t0004g0012 a0004c0006t0004g0330 a0004c0006t0004g0331 others(3): Show |
6 | HG01192.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+7340delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011887 | |||||||
| chr13:41011918 | C | A | 64 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0207 others(61): Show |
65 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.-229+7310G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41011918 | |||||||
| chr13:41012047 | C | T | 1 | a0001c0001t0007g0344 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-229+7181G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012047 | |||||||
| chr13:41012262 | G | A | 1 | a0002c0002t0002g0046 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-229+6966C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012262 | |||||||
| chr13:41012274 | C | T | 16 | a0001c0001t0001g0062 a0001c0001t0007g0344 a0001c0005t0003g0336 others(13): Show |
16 | HG01192.hp2 HG02717.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.-229+6954G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012274 | |||||||
| chr13:41012312 | C | CA | 19 | a0001c0001t0001g0115 a0001c0001t0001g0304 a0001c0001t0002g0111 others(16): Show |
19 | HG01192.hp2 HG01981.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-229+6915dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012312 | |||||||
| chr13:41012312 | CA | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.-229+6915delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012312 | |||||||
| chr13:41012312 | CAA | C | 72 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(69): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-229+6914_-229+691 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012312 | |||||||
| chr13:41012312 | CAAAAAA | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0346 a0001c0001t0001g0347 others(1): Show |
6 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+6910_-229+691 others(10): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012312 | |||||||
| chr13:41012312 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0083 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-229+6904_-229+691 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012312 | |||||||
| chr13:41012545 | CT | C | 52 | a0001c0001t0001g0073 a0001c0001t0001g0158 a0001c0001t0001g0165 others(49): Show |
53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.-229+6682delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012545 | |||||||
| chr13:41012668 | C | T | 84 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0077 others(81): Show |
86 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-229+6560G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012668 | |||||||
| chr13:41012688 | A | C | 1 | a0001c0001t0013g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-229+6540T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012688 | |||||||
| chr13:41012689 | GTGTGACA others(12): Show |
G | 1 | a0001c0001t0001g0179 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-229+6520_-229+653 others(23): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012689 | |||||||
| chr13:41012736 | C | T | 1 | a0002c0002t0002g0181 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-229+6492G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012736 | |||||||
| chr13:41012778 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-229+6450C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012778 | |||||||
| chr13:41012824 | C | T | 69 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0207 others(66): Show |
70 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-229+6404G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012824 | |||||||
| chr13:41012919 | T | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(324): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-229+6309A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41012919 | |||||||
| chr13:41013239 | T | C | 7 | a0002c0002t0002g0024 a0002c0002t0002g0043 a0002c0002t0002g0044 others(4): Show |
7 | HG00733.hp2 HG00738.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+5989A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013239 | |||||||
| chr13:41013260 | C | A | 4 | a0001c0001t0014g0283 a0001c0003t0001g0078 a0001c0003t0001g0282 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-229+5968G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013260 | |||||||
| chr13:41013326 | G | A | 2 | a0002c0002t0002g0048 a0002c0002t0002g0049 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-229+5902C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013326 | |||||||
| chr13:41013336 | T | C | 1 | a0002c0002t0002g0231 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-229+5892A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013336 | |||||||
| chr13:41013712 | A | G | 45 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0058 others(42): Show |
47 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.-229+5516T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013712 | |||||||
| chr13:41013918 | A | C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0288 a0001c0001t0001g0304 |
3 | NA18941.hp1 NA19065.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-229+5310T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013918 | |||||||
| chr13:41013960 | A | T | 3 | a0001c0001t0001g0234 a0001c0001t0001g0236 a0001c0001t0009g0235 |
3 | HG02615.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-229+5268T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41013960 | |||||||
| chr13:41014294 | C | T | 1 | a0002c0002t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-229+4934G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014294 | |||||||
| chr13:41014301 | C | A | 1 | a0001c0001t0013g0281 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-229+4927G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014301 | |||||||
| chr13:41014301 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-229+4927G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014301 | |||||||
| chr13:41014326 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
130 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.-229+4902A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014326 | |||||||
| chr13:41014696 | G | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
60 | HG00438.hp2 HG00597.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.-229+4532C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41014696 | |||||||
| chr13:41015155 | G | A | 9 | a0001c0001t0007g0344 a0001c0005t0003g0336 a0001c0005t0003g0337 others(6): Show |
9 | HG03491.hp1 HG03834.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+4073C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015155 | |||||||
| chr13:41015261 | G | A | 2 | a0002c0002t0002g0232 a0002c0002t0002g0233 |
2 | NA18943.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-229+3967C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015261 | |||||||
| chr13:41015335 | C | CA | 7 | a0001c0001t0001g0316 a0002c0002t0002g0022 a0002c0002t0002g0051 others(4): Show |
7 | HG01071.hp2 HG01517.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+3892dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015335 | |||||||
| chr13:41015362 | T | A | 6 | a0004c0006t0004g0012 a0004c0006t0004g0330 a0004c0006t0004g0331 others(3): Show |
6 | HG01192.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+3866A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015362 | |||||||
| chr13:41015403 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-229+3825T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015403 | |||||||
| chr13:41015491 | G | T | 10 | a0001c0001t0001g0062 a0001c0001t0007g0344 a0001c0005t0003g0336 others(7): Show |
10 | HG02723.hp1 HG03491.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.-229+3737C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015491 | |||||||
| chr13:41015918 | G | C | 3 | a0001c0001t0007g0110 a0002c0002t0002g0108 a0002c0002t0002g0109 |
3 | HG03017.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-229+3310C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015918 | |||||||
| chr13:41015930 | GAAT | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0077 others(81): Show |
86 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-229+3295_-229+329 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015930 | |||||||
| chr13:41015960 | A | G | 1 | a0002c0002t0002g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-229+3268T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41015960 | |||||||
| chr13:41016147 | C | T | 1 | a0003c0018t0003g0026 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-229+3081G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016147 | |||||||
| chr13:41016196 | T | C | 6 | a0004c0006t0004g0012 a0004c0006t0004g0330 a0004c0006t0004g0331 others(3): Show |
6 | HG01192.hp2 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-229+3032A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016196 | |||||||
| chr13:41016252 | C | T | 10 | a0001c0001t0001g0062 a0001c0001t0007g0344 a0001c0005t0003g0336 others(7): Show |
10 | HG02723.hp1 HG03491.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.-229+2976G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016252 | |||||||
| chr13:41016271 | G | A | 1 | a0007c0015t0002g0025 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-229+2957C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016271 | |||||||
| chr13:41016417 | C | A | 4 | a0001c0001t0014g0283 a0001c0003t0001g0078 a0001c0003t0001g0282 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-229+2811G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016417 | |||||||
| chr13:41016542 | G | T | 10 | a0001c0001t0001g0062 a0001c0001t0007g0344 a0001c0005t0003g0336 others(7): Show |
10 | HG02723.hp1 HG03491.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.-229+2686C>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016542 | |||||||
| chr13:41016572 | T | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(344): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.-229+2656A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016572 | |||||||
| chr13:41016689 | C | A | 2 | a0001c0001t0001g0285 a0001c0001t0008g0284 |
2 | HG02572.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-229+2539G>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016689 | |||||||
| chr13:41016756 | A | T | 5 | a0001c0001t0007g0110 a0002c0002t0002g0106 a0002c0002t0002g0107 others(2): Show |
5 | HG00609.hp2 HG03017.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.-229+2472T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016756 | |||||||
| chr13:41016821 | G | A | 1 | a0001c0003t0001g0303 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-229+2407C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016821 | |||||||
| chr13:41016867 | T | C | 1 | a0002c0002t0002g0286 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-229+2361A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016867 | |||||||
| chr13:41016914 | C | CA | 23 | a0001c0001t0001g0009 a0001c0001t0001g0058 a0001c0001t0001g0287 others(20): Show |
24 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.-229+2313dupT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016914 | C | CAA | 8 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(5): Show |
8 | HG00438.hp2 HG01071.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.-229+2312_-229+231 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016914 | CA | C | 17 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(14): Show |
17 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(14): Show |
intron_variant | MODIFIER | c.-229+2313delT | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016914 | CAA | C | 11 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(8): Show |
11 | HG01109.hp2 HG02056.hp2 NA18971.hp2 others(8): Show |
intron_variant | MODIFIER | c.-229+2312_-229+231 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016914 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | NA18747.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-229+2304_-229+231 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016914 | CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0001g0078 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-229+2302_-229+231 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016914 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0077 |
2 | HG02723.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.-229+2301_-229+231 others(17): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016914 | CAAAAAAA others(7): Show |
C | 2 | a0001c0001t0001g0075 a0005c0007t0001g0076 |
2 | NA19083.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-229+2300_-229+231 others(18): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016914 | CAAAAAAA others(8): Show |
C | 1 | a0002c0002t0002g0074 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-229+2299_-229+231 others(19): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016914 | CAAAAAAA others(9): Show |
C | 9 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(6): Show |
9 | HG02071.hp2 HG03225.hp2 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+2298_-229+231 others(20): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016914 | CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0064 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-229+2296_-229+231 others(22): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016914 | |||||||
| chr13:41016935 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0335 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-229+2279_-229+229 others(18): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016935 | |||||||
| chr13:41016935 | AAAAAAAA others(25): Show |
A | 1 | a0001c0003t0001g0325 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-229+2261_-229+229 others(36): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016935 | |||||||
| chr13:41016936 | AAAAAAAA others(8): Show |
A | 1 | a0002c0002t0002g0221 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-229+2277_-229+229 others(19): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016936 | |||||||
| chr13:41016937 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-229+2291T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016937 | |||||||
| chr13:41016937 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0014g0283 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-229+2279_-229+229 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016937 | |||||||
| chr13:41016938 | AAAAAAAA others(4): Show |
A | 1 | a0001c0003t0001g0282 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-229+2279_-229+228 others(15): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016938 | |||||||
| chr13:41016939 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0239 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-229+2288_-229+228 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016939 | |||||||
| chr13:41016939 | A | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | NA18747.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-229+2289T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016939 | |||||||
| chr13:41016939 | AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0015g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-229+2269_-229+228 others(24): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016939 | |||||||
| chr13:41016940 | AAAAAAAA others(4): Show |
A | 1 | a0001c0005t0003g0342 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-229+2277_-229+228 others(15): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016940 | |||||||
| chr13:41016940 | AAAAAAAA others(14): Show |
A | 1 | a0004c0006t0004g0010 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-229+2267_-229+228 others(25): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016940 | |||||||
| chr13:41016941 | A | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0075 a0001c0001t0001g0079 others(2): Show |
5 | HG02723.hp1 NA18747.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-229+2287T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016941 | |||||||
| chr13:41016941 | AAAAAAAA others(1): Show |
A | 7 | a0001c0001t0001g0038 a0002c0002t0002g0209 a0002c0002t0002g0215 others(4): Show |
7 | HG01106.hp1 HG01433.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.-229+2279_-229+228 others(12): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016941 | |||||||
| chr13:41016941 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0007g0110 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-229+2277_-229+228 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016941 | |||||||
| chr13:41016941 | AAAAAAAA others(5): Show |
A | 1 | a0001c0005t0003g0338 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-229+2275_-229+228 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016941 | |||||||
| chr13:41016942 | AAAAAAAT others(4): Show |
A | 6 | a0001c0005t0003g0336 a0001c0005t0003g0337 a0001c0005t0003g0339 others(3): Show |
6 | HG03834.hp2 NA18612.hp1 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.-229+2275_-229+228 others(15): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016942 | |||||||
| chr13:41016942 | AAAAAAAT others(14): Show |
A | 1 | a0001c0001t0008g0143 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-229+2265_-229+228 others(25): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016942 | |||||||
| chr13:41016943 | A | ATAT | 3 | a0001c0001t0001g0240 a0001c0001t0001g0267 a0001c0001t0008g0284 |
3 | HG01934.hp2 HG02630.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.-229+2284_-229+228 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016943 | |||||||
| chr13:41016943 | A | ATATAT | 3 | a0001c0001t0001g0242 a0001c0001t0001g0257 a0001c0003t0001g0153 |
3 | NA18945.hp1 NA19007.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-229+2284_-229+228 others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016943 | |||||||
| chr13:41016943 | A | T | 12 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(9): Show |
12 | HG02717.hp2 HG02738.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.-229+2285T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016943 | |||||||
| chr13:41016943 | AAAAAATA others(3): Show |
A | 3 | a0001c0001t0007g0344 a0002c0002t0002g0108 a0002c0002t0002g0109 |
3 | HG03491.hp1 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-229+2275_-229+228 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016943 | |||||||
| chr13:41016943 | AAAAAATA others(7): Show |
A | 1 | a0002c0002t0002g0114 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-229+2271_-229+228 others(18): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016943 | |||||||
| chr13:41016944 | AAAAAT | A | 7 | a0001c0001t0001g0219 a0001c0001t0001g0329 a0002c0002t0002g0199 others(4): Show |
7 | HG00673.hp2 HG02615.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+2279_-229+228 others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016944 | |||||||
| chr13:41016944 | AAAAATAT others(4): Show |
A | 1 | a0001c0001t0001g0328 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-229+2273_-229+228 others(15): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016944 | |||||||
| chr13:41016945 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0272 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-229+2282_-229+228 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | |||||||
| chr13:41016945 | A | AATATATA others(5): Show |
1 | a0001c0003t0001g0164 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-229+2282_-229+228 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | |||||||
| chr13:41016945 | A | AT | 6 | a0001c0001t0001g0122 a0001c0001t0001g0165 a0001c0001t0001g0276 others(3): Show |
7 | HG01346.hp1 HG01358.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+2282_-229+228 others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | |||||||
| chr13:41016945 | A | T | 43 | a0001c0001t0001g0013 a0001c0001t0001g0062 a0001c0001t0001g0065 others(40): Show |
43 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.-229+2283T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | |||||||
| chr13:41016945 | AAAATAT | A | 8 | a0001c0001t0001g0218 a0002c0002t0002g0185 a0002c0002t0002g0190 others(5): Show |
8 | HG03239.hp2 NA18953.hp2 NA18957.hp2 others(5): Show |
intron_variant | MODIFIER | c.-229+2277_-229+228 others(10): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | |||||||
| chr13:41016945 | AAAATATA others(1): Show |
A | 11 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0259 others(8): Show |
11 | HG00140.hp2 HG00738.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-229+2275_-229+228 others(12): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | |||||||
| chr13:41016945 | AAAATATA others(3): Show |
A | 1 | a0002c0002t0002g0231 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-229+2273_-229+228 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016945 | |||||||
| chr13:41016947 | A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0128 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-229+2280_-229+228 others(16): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | |||||||
| chr13:41016947 | A | AAAT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(8): Show |
14 | HG01358.hp2 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-229+2280_-229+228 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | |||||||
| chr13:41016947 | A | AAATATAT others(4): Show |
2 | a0002c0002t0002g0004 a0004c0006t0004g0177 |
2 | HG02630.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-229+2280_-229+228 others(15): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | |||||||
| chr13:41016947 | A | AAT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0123 others(13): Show |
16 | HG01109.hp1 HG01346.hp2 HG04228.hp2 others(13): Show |
intron_variant | MODIFIER | c.-229+2279_-229+228 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | |||||||
| chr13:41016947 | A | AATATATA others(3): Show |
1 | a0002c0002t0002g0004 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-229+2271_-229+228 others(14): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | |||||||
| chr13:41016947 | A | AT | 10 | a0001c0001t0001g0135 a0001c0001t0001g0138 a0001c0003t0001g0166 others(7): Show |
11 | HG00642.hp2 HG01433.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.-229+2280_-229+228 others(5): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | |||||||
| chr13:41016947 | A | ATAT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0134 a0001c0001t0001g0140 others(8): Show |
11 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-229+2280_-229+228 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | |||||||
| chr13:41016947 | A | ATATAT | 3 | a0001c0001t0001g0234 a0001c0001t0001g0277 a0002c0002t0002g0046 |
3 | HG02615.hp1 HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-229+2280_-229+228 others(9): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | |||||||
| chr13:41016947 | A | T | 81 | a0001c0001t0001g0013 a0001c0001t0001g0064 a0001c0001t0001g0065 others(78): Show |
82 | HG00280.hp2 HG00408.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.-229+2281T>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | |||||||
| chr13:41016947 | AAT | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0264 a0001c0001t0001g0310 others(8): Show |
11 | HG01169.hp2 HG01884.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.-229+2279_-229+228 others(6): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016947 | |||||||
| chr13:41016948 | AT | A | 9 | a0001c0001t0001g0132 a0001c0001t0001g0245 a0001c0001t0001g0309 others(6): Show |
9 | HG00733.hp1 HG01070.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.-229+2279delA | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016948 | |||||||
| chr13:41016948 | ATAT | A | 4 | a0001c0001t0001g0117 a0001c0003t0001g0015 a0001c0003t0001g0016 others(1): Show |
4 | HG01070.hp1 HG01071.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.-229+2277_-229+227 others(7): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016948 | |||||||
| chr13:41016948 | ATATATAT | A | 4 | a0001c0001t0001g0139 a0001c0003t0001g0324 a0002c0002t0002g0194 others(1): Show |
4 | NA18961.hp2 NA18991.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-229+2273_-229+227 others(11): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016948 | |||||||
| chr13:41016949 | T | A | 14 | a0001c0001t0001g0119 a0001c0001t0001g0130 a0001c0001t0001g0149 others(11): Show |
14 | HG00544.hp1 HG02132.hp2 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.-229+2279A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016949 | |||||||
| chr13:41016951 | T | A | 11 | a0001c0001t0001g0062 a0001c0001t0001g0309 a0001c0001t0001g0310 others(8): Show |
11 | HG01169.hp2 HG02027.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-229+2277A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016951 | |||||||
| chr13:41016953 | T | A | 4 | a0001c0003t0001g0318 a0002c0002t0002g0317 a0002c0002t0002g0319 others(1): Show |
4 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.-229+2275A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016953 | |||||||
| chr13:41016955 | T | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0320 a0001c0001t0001g0321 others(1): Show |
4 | HG00735.hp2 HG02723.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.-229+2273A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016955 | |||||||
| chr13:41016957 | T | A | 2 | a0001c0003t0001g0324 a0002c0002t0002g0323 |
2 | NA18991.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-229+2271A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016957 | |||||||
| chr13:41016959 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-229+2269A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016959 | |||||||
| chr13:41016963 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-229+2265A>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016963 | |||||||
| chr13:41016977 | T | C | 1 | a0001c0001t0011g0326 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-229+2251A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016977 | |||||||
| chr13:41016982 | G | A | 7 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0087 others(4): Show |
7 | NA18959.hp1 NA18997.hp2 NA19003.hp1 others(4): Show |
intron_variant | MODIFIER | c.-229+2246C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41016982 | |||||||
| chr13:41017099 | A | C | 10 | a0001c0001t0001g0062 a0001c0001t0007g0344 a0001c0005t0003g0336 others(7): Show |
10 | HG02723.hp1 HG03491.hp1 HG03834.hp2 others(7): Show |
intron_variant | MODIFIER | c.-229+2129T>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017099 | |||||||
| chr13:41017140 | T | C | 10 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(7): Show |
10 | HG01192.hp2 HG02615.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-229+2088A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017140 | |||||||
| chr13:41017278 | C | T | 7 | a0002c0002t0002g0003 a0002c0002t0002g0017 a0002c0002t0002g0018 others(4): Show |
8 | HG00642.hp2 HG01109.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-229+1950G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017278 | |||||||
| chr13:41017587 | C | G | 47 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0058 others(44): Show |
49 | HG00280.hp1 HG00621.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-229+1641G>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017587 | |||||||
| chr13:41017630 | C | T | 2 | a0001c0003t0001g0015 a0001c0003t0001g0016 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-229+1598G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017630 | |||||||
| chr13:41017741 | G | A | 9 | a0001c0001t0007g0344 a0001c0005t0003g0336 a0001c0005t0003g0337 others(6): Show |
9 | HG03491.hp1 HG03834.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+1487C>T | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017741 | |||||||
| chr13:41017777 | T | C | 1 | a0001c0001t0001g0345 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-229+1451A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41017777 | |||||||
| chr13:41018146 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0346 others(4): Show |
9 | HG01884.hp2 HG01981.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-229+1082A>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41018146 | |||||||
| chr13:41018179 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-229+1049G>A | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41018179 | |||||||
| chr13:41018211 | C | CAGAAATA others(33): Show |
1 | a0001c0001t0001g0013 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-229+977_-229+1016 others(43): Show |
ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41018211 | |||||||
| chr13:41018494 | G | C | 1 | a0002c0002t0002g0351 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-229+734C>G | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41018494 | |||||||
| chr13:41019002 | A | G | 3 | a0001c0001t0015g0011 a0004c0006t0004g0010 a0004c0006t0004g0012 |
3 | HG01496.hp2 HG02559.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-229+226T>C | ELF1 | ENSG00000120690.16 | transcript | ENST00000239882.7 | protein_coding | 1/8 | chr13 | 41019002 |