Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1871 |
| ensemblid | ENSG00000112242.16 |
| hgncid | 3115 |
| symbol | E2F3 |
| name | E2F transcription factor 3 |
| refseq_nuc | NM_001949.5 |
| refseq_prot | NP_001940.1 |
| ensembl_nuc | ENST00000346618.8 |
| ensembl_prot | ENSP00000262904.4 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 20401879 |
| end | 20493714 |
| strand | + |
| ver | v1.2 |
| region | chr6:20401879-20493714 |
| region5000 | chr6:20396879-20498714 |
| regionname0 | E2F3_chr6_20401879_20493714 |
| regionname5000 | E2F3_chr6_20396879_20498714 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 465 | 323 | 89 | 55 | 127 | 11 | 39 | 100 | E2F3_chr6_20396879_20498714 | E2F3 | MRKGI others(460): Show |
chr6 | 20396879 | 20498714 |
| a0002 | 0/0 | 462 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | MRKGI others(457): Show |
chr6 | 20396879 | 20498714 |
| a0003 | 0/0 | 465 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | MRKGI others(460): Show |
chr6 | 20396879 | 20498714 |
| a0004 | 0/0 | 465 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | MRKGI others(460): Show |
chr6 | 20396879 | 20498714 |
| a0005 | 0/0 | 465 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | MRKGI others(460): Show |
chr6 | 20396879 | 20498714 |
| a0006 | 0/0 | 465 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | MRKGI others(460): Show |
chr6 | 20396879 | 20498714 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1395 | 321 | 89 | 54 | 126 | 11 | 39 | E2F3_chr6_20396879_20498714 | E2F3 | ATGAG others(1390): Show |
chr6 | 20396879 | 20498714 | ||
| a0001c0007 | 0/0 | 1395 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATGAG others(1390): Show |
chr6 | 20396879 | 20498714 | ||
| a0001c0008 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATGAG others(1390): Show |
chr6 | 20396879 | 20498714 | ||
| a0002c0002 | 0/0 | 1386 | 4 | 3 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATGAG others(1381): Show |
chr6 | 20396879 | 20498714 | ||
| a0003c0003 | 0/0 | 1395 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATGAG others(1390): Show |
chr6 | 20396879 | 20498714 | ||
| a0004c0004 | 0/0 | 1395 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATGAG others(1390): Show |
chr6 | 20396879 | 20498714 | ||
| a0005c0005 | 0/0 | 1395 | 2 | 0 | 0 | 1 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | ATGAG others(1390): Show |
chr6 | 20396879 | 20498714 | ||
| a0006c0006 | 0/0 | 1395 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATGAG others(1390): Show |
chr6 | 20396879 | 20498714 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5036 | 179 | 46 | 32 | 70 | 7 | 24 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0002 | 1/0 | 5036 | 56 | 2 | 10 | 30 | 4 | 9 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0003 | 0/0 | 5036 | 21 | 20 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0004 | 0/0 | 5036 | 11 | 0 | 0 | 8 | 0 | 3 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0005 | 0/0 | 5037 | 10 | 3 | 7 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5032): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0006 | 0/0 | 5036 | 8 | 1 | 0 | 7 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0007 | 0/0 | 5036 | 6 | 5 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0008 | 0/0 | 5036 | 6 | 4 | 2 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0009 | 0/0 | 5036 | 3 | 0 | 0 | 3 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0010 | 0/0 | 5036 | 2 | 0 | 0 | 2 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0011 | 0/0 | 5037 | 2 | 0 | 1 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5032): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0012 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0013 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0014 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0015 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0016 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0017 | 0/0 | 5037 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5032): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0018 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0019 | 0/0 | 5037 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5032): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0020 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0021 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0022 | 0/1 | 5036 | 1 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0023 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0024 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0025 | 0/0 | 5037 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5032): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0026 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0027 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0001t0028 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0007t0002 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0001c0008t0001 | 0/0 | 5036 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0002c0002t0001 | 0/0 | 5027 | 3 | 2 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5022): Show |
chr6 | 20396879 | 20498714 |
| a0002c0002t0003 | 0/0 | 5027 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5022): Show |
chr6 | 20396879 | 20498714 |
| a0003c0003t0001 | 0/0 | 5036 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0004c0004t0001 | 0/0 | 5036 | 2 | 2 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0004c0004t0007 | 0/0 | 5036 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0005c0005t0001 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0005c0005t0004 | 0/0 | 5036 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| a0006c0006t0002 | 0/0 | 5036 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | ATTCA others(5031): Show |
chr6 | 20396879 | 20498714 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0005g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0006g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0007g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0008g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0008g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0009g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0009g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0009g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0010g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0010g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0011g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0011g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0012g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0013g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0014g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0015g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0016g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0017g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0018g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0019g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0020g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0021g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0022g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0023g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0024g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0025g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0026g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0027g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0001t0028g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0007t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0001c0008t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0002c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0003c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0003c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0004c0004t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0004c0004t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0005c0005t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0005c0005t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| a0006c0006t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0223 | EUR | GBR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0317 | EUR | GBR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0298 | EUR | GBR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00140 | hp2 | a0006 | c0006 | t0002 | g0018 | EUR | GBR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0233 | EUR | FIN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0130 | EUR | FIN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | FIN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0318 | EUR | FIN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00438 | hp2 | a0001 | c0001 | t0014 | g0218 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00544 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | CHS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01081 | hp1 | a0001 | c0008 | t0001 | g0160 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0103 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01175 | hp1 | a0001 | c0001 | t0005 | g0288 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0293 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01192 | hp1 | a0001 | c0001 | t0005 | g0294 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0290 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0076 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01358 | hp2 | a0001 | c0001 | t0005 | g0136 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | IBS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0299 | EUR | IBS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01884 | hp1 | a0001 | c0001 | t0024 | g0308 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0102 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01975 | hp1 | a0001 | c0001 | t0011 | g0247 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0039 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02040 | hp2 | a0001 | c0001 | t0006 | g0152 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02056 | hp1 | a0001 | c0001 | t0006 | g0260 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0261 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02129 | hp2 | a0005 | c0005 | t0004 | g0178 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0181 | EAS | CDX | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CDX | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0320 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0123 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0212 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02451 | hp2 | a0001 | c0001 | t0026 | g0328 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02523 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | KHV | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02572 | hp1 | a0001 | c0001 | t0028 | g0110 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0141 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02615 | hp2 | a0001 | c0001 | t0021 | g0104 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0146 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02630 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0117 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02647 | hp2 | a0001 | c0001 | t0020 | g0144 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02717 | hp2 | a0004 | c0004 | t0007 | g0321 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0075 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0098 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0081 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0239 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0329 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03209 | hp1 | a0001 | c0001 | t0017 | g0306 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0322 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03453 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03540 | hp1 | a0001 | c0001 | t0023 | g0137 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03579 | hp1 | a0001 | c0001 | t0025 | g0071 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03654 | hp1 | a0001 | c0001 | t0016 | g0219 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0058 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0268 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03834 | hp2 | a0001 | c0001 | t0013 | g0236 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03942 | hp1 | a0001 | c0001 | t0012 | g0065 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03942 | hp2 | a0005 | c0005 | t0001 | g0147 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0267 | SAS | BEB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0272 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0070 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | CHB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0122 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18970 | hp2 | a0001 | c0001 | t0010 | g0222 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18984 | hp2 | a0001 | c0001 | t0018 | g0213 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18992 | hp1 | a0001 | c0001 | t0019 | g0208 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18995 | hp2 | a0001 | c0001 | t0009 | g0286 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18997 | hp1 | a0001 | c0001 | t0027 | g0036 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19002 | hp2 | a0001 | c0001 | t0015 | g0192 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19007 | hp1 | a0001 | c0007 | t0002 | g0232 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19011 | hp2 | a0001 | c0001 | t0009 | g0274 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19030 | hp1 | a0002 | c0002 | t0003 | g0091 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0323 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19058 | hp1 | a0001 | c0001 | t0011 | g0025 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0262 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19070 | hp2 | a0001 | c0001 | t0010 | g0225 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0197 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0319 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0313 | AFR | ASW | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ASW | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | GIH | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | GIH | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0069 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0263 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | MSL | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | USA | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | USA | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | USA | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | USA | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | LWK | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0022 | g0264 | REF | REF | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0159 | REF | REF | E2F3_chr6_20396879_20498714 | E2F3 | chr6 | 20396879 | 20498714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:20402363 | TCGCCGCC others(2): Show |
T | 1 | a0002 | 4 | HG01255.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.141_149delCGCCGCCG others(1): Show |
p.Ala48_Ala50del | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/7 | 495/5036 | 141/1398 | 47/465 | INFO_REALIGN_3_PRIME | chr6 | 20402363 | ||
| chr6:20402458 | A | G | 1 | a0005 | 2 | HG02129.hp2 HG03942.hp2 |
missense_variant | MODERATE | c.226A>G | p.Ser76Gly | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/7 | 580/5036 | 226/1398 | 76/465 | chr6 | 20402458 | |||
| chr6:20402579 | C | T | 1 | a0004 | 3 | HG02630.hp1 HG02717.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.347C>T | p.Pro116Leu | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/7 | 701/5036 | 347/1398 | 116/465 | chr6 | 20402579 | |||
| chr6:20490197 | G | A | 1 | a0006 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.1165G>A | p.Asp389Asn | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1519/5036 | 1165/1398 | 389/465 | chr6 | 20490197 | |||
| chr6:20490212 | A | T | 1 | a0003 | 3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.1180A>T | p.Met394Leu | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1534/5036 | 1180/1398 | 394/465 | chr6 | 20490212 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:20402505 | G | T | 1 | a0001c0008 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.273G>T | p.Ala91Ala | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/7 | 627/5036 | 273/1398 | 91/465 | chr6 | 20402505 | |||
| chr6:20479911 | C | T | 1 | a0001c0007 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.459C>T | p.Pro153Pro | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/7 | 813/5036 | 459/1398 | 153/465 | chr6 | 20479911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:20401946 | C | T | 1 | a0001c0001t0028 | 1 | HG02572.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-287C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/7 | chr6 | 20401946 | |||||||
| chr6:20490562 | G | T | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*132G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 132 | chr6 | 20490562 | ||||||
| chr6:20490563 | A | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*133A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 133 | chr6 | 20490563 | ||||||
| chr6:20490565 | G | T | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*135G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 135 | chr6 | 20490565 | ||||||
| chr6:20490575 | A | T | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*145A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 145 | chr6 | 20490575 | ||||||
| chr6:20490576 | T | C | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*146T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 146 | chr6 | 20490576 | ||||||
| chr6:20490579 | T | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*149T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 149 | chr6 | 20490579 | ||||||
| chr6:20490580 | A | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*150A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 150 | chr6 | 20490580 | ||||||
| chr6:20490582 | T | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*152T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 152 | chr6 | 20490582 | ||||||
| chr6:20490586 | T | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*156T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 156 | chr6 | 20490586 | ||||||
| chr6:20490587 | T | A | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*157T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 157 | chr6 | 20490587 | ||||||
| chr6:20490588 | T | A | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*158T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 158 | chr6 | 20490588 | ||||||
| chr6:20490589 | T | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*159T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 159 | chr6 | 20490589 | ||||||
| chr6:20490590 | T | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*160T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 160 | chr6 | 20490590 | ||||||
| chr6:20490592 | A | T | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 162 | chr6 | 20490592 | ||||||
| chr6:20490594 | A | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*164A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 164 | chr6 | 20490594 | ||||||
| chr6:20490598 | T | C | 2 | a0001c0001t0012 a0001c0001t0013 |
2 | HG03834.hp2 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*168T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 168 | chr6 | 20490598 | ||||||
| chr6:20490598 | T | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*168T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 168 | chr6 | 20490598 | ||||||
| chr6:20490599 | T | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*169T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 169 | chr6 | 20490599 | ||||||
| chr6:20490600 | A | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*170A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 170 | chr6 | 20490600 | ||||||
| chr6:20490602 | T | C | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*172T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 172 | chr6 | 20490602 | ||||||
| chr6:20490610 | T | C | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*180T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 180 | chr6 | 20490610 | ||||||
| chr6:20490618 | A | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 188 | chr6 | 20490618 | ||||||
| chr6:20490619 | C | A | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*189C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 189 | chr6 | 20490619 | ||||||
| chr6:20490620 | G | C | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*190G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 190 | chr6 | 20490620 | ||||||
| chr6:20490623 | C | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 193 | chr6 | 20490623 | ||||||
| chr6:20490628 | G | C | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*198G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 198 | chr6 | 20490628 | ||||||
| chr6:20490628 | G | T | 1 | a0001c0001t0026 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*198G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 198 | chr6 | 20490628 | ||||||
| chr6:20490629 | C | T | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*199C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 199 | chr6 | 20490629 | ||||||
| chr6:20490630 | A | G | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 200 | chr6 | 20490630 | ||||||
| chr6:20490632 | G | T | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*202G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 202 | chr6 | 20490632 | ||||||
| chr6:20491162 | C | T | 1 | a0001c0001t0009 | 3 | NA18995.hp2 NA19011.hp2 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*732C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 732 | chr6 | 20491162 | ||||||
| chr6:20491356 | C | T | 1 | a0001c0001t0025 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*926C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 926 | chr6 | 20491356 | ||||||
| chr6:20491446 | G | A | 1 | a0001c0001t0027 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1016G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1016 | chr6 | 20491446 | ||||||
| chr6:20491552 | G | A | 1 | a0001c0001t0014 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1122G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1122 | chr6 | 20491552 | ||||||
| chr6:20491642 | G | T | 1 | a0001c0001t0024 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1212G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1212 | chr6 | 20491642 | ||||||
| chr6:20491679 | A | G | 1 | a0001c0001t0006 | 8 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1249A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1249 | chr6 | 20491679 | ||||||
| chr6:20491976 | G | A | 2 | a0001c0001t0007 a0004c0004t0007 |
7 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1546G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1546 | chr6 | 20491976 | ||||||
| chr6:20492029 | C | G | 1 | a0001c0001t0023 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1599C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1599 | chr6 | 20492029 | ||||||
| chr6:20492149 | G | GA | 1 | a0001c0001t0005 | 10 | HG01175.hp1 HG01175.hp2 HG01192.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1731dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1732 | INFO_REALIGN_3_PRIME | chr6 | 20492149 | |||||
| chr6:20492176 | C | G | 2 | a0001c0001t0004 a0005c0005t0004 |
12 | HG02040.hp1 HG02129.hp2 HG03654.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1746C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 1746 | chr6 | 20492176 | ||||||
| chr6:20492764 | T | C | 32 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(29): Show |
274 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*2334T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2334 | chr6 | 20492764 | ||||||
| chr6:20492774 | G | A | 1 | a0001c0001t0008 | 6 | HG00642.hp2 HG01081.hp2 HG02109.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2344G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2344 | chr6 | 20492774 | ||||||
| chr6:20492920 | T | C | 1 | a0001c0001t0015 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2490T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2490 | chr6 | 20492920 | ||||||
| chr6:20492982 | C | T | 1 | a0001c0001t0023 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2552C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2552 | chr6 | 20492982 | ||||||
| chr6:20493004 | G | A | 1 | a0001c0001t0016 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2574G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2574 | chr6 | 20493004 | ||||||
| chr6:20493078 | C | T | 1 | a0001c0001t0021 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2648C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2648 | chr6 | 20493078 | ||||||
| chr6:20493230 | T | C | 7 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0012 others(4): Show |
32 | HG00738.hp1 HG01109.hp1 HG01884.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2800T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2800 | chr6 | 20493230 | ||||||
| chr6:20493233 | G | T | 1 | a0001c0001t0020 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2803G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 2803 | chr6 | 20493233 | ||||||
| chr6:20493447 | G | A | 1 | a0001c0001t0018 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3017G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 3017 | chr6 | 20493447 | ||||||
| chr6:20493555 | A | G | 1 | a0001c0001t0010 | 2 | NA18970.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3125A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 3125 | chr6 | 20493555 | ||||||
| chr6:20493558 | T | TA | 4 | a0001c0001t0011 a0001c0001t0017 a0001c0001t0019 others(1): Show |
5 | HG01975.hp1 HG03209.hp1 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3137dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 3138 | INFO_REALIGN_3_PRIME | chr6 | 20493558 | |||||
| chr6:20493567 | AC | A | 8 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(5): Show |
63 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3138delC | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 3138 | chr6 | 20493567 | ||||||
| chr6:20493568 | C | A | 3 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0015 |
22 | HG00544.hp2 HG01975.hp2 HG01978.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3138C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 7/7 | 3138 | chr6 | 20493568 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:20402751 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.393+126T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20402751 | |||||||
| chr6:20402843 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0003g0008 a0001c0001t0003g0009 |
3 | HG02723.hp2 HG02895.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.393+218G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20402843 | |||||||
| chr6:20403046 | G | T | 2 | a0001c0001t0007g0329 a0001c0001t0026g0328 |
2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.393+421G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403046 | |||||||
| chr6:20403220 | C | T | 3 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 |
3 | NA18955.hp1 NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.393+595C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403220 | |||||||
| chr6:20403253 | G | A | 1 | a0001c0001t0002g0011 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.393+628G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403253 | |||||||
| chr6:20403301 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.393+676C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403301 | |||||||
| chr6:20403356 | G | T | 6 | a0001c0001t0003g0319 a0001c0001t0003g0320 a0001c0001t0003g0323 others(3): Show |
7 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+731G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403356 | |||||||
| chr6:20403547 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.393+922G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403547 | |||||||
| chr6:20403582 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.393+957A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403582 | |||||||
| chr6:20403711 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.393+1086C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403711 | |||||||
| chr6:20403715 | C | T | 9 | a0001c0001t0001g0310 a0001c0001t0001g0311 a0001c0001t0001g0312 others(6): Show |
9 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+1090C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403715 | |||||||
| chr6:20403915 | G | T | 2 | a0001c0001t0001g0307 a0001c0001t0017g0306 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.393+1290G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20403915 | |||||||
| chr6:20404012 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0003g0001 a0001c0001t0003g0014 |
5 | HG01361.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+1387T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404012 | |||||||
| chr6:20404048 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.393+1423G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404048 | |||||||
| chr6:20404114 | A | AG | 85 | a0001c0001t0001g0012 a0001c0001t0001g0227 a0001c0001t0001g0234 others(82): Show |
85 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.393+1494dupG | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20404114 | ||||||
| chr6:20404189 | T | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(243): Show |
252 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.393+1564T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404189 | |||||||
| chr6:20404251 | C | T | 1 | a0003c0003t0001g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.393+1626C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404251 | |||||||
| chr6:20404651 | G | C | 1 | a0005c0005t0001g0147 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.393+2026G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404651 | |||||||
| chr6:20404714 | AG | A | 54 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(51): Show |
54 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.393+2090delG | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404714 | |||||||
| chr6:20404762 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.393+2137C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404762 | |||||||
| chr6:20404788 | G | A | 223 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(220): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.393+2163G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20404788 | |||||||
| chr6:20405035 | A | C | 11 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(8): Show |
11 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.393+2410A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405035 | |||||||
| chr6:20405308 | A | G | 185 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(182): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.393+2683A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405308 | |||||||
| chr6:20405344 | A | AT | 11 | a0001c0001t0001g0092 a0001c0001t0001g0145 a0001c0001t0001g0217 others(8): Show |
11 | HG00099.hp1 HG00438.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.393+2739dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20405344 | ||||||
| chr6:20405344 | AT | A | 30 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(27): Show |
30 | HG00738.hp1 HG01167.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.393+2739delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20405344 | ||||||
| chr6:20405344 | ATT | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(171): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.393+2738_393+2739d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20405344 | ||||||
| chr6:20405415 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.393+2790C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405415 | |||||||
| chr6:20405563 | G | A | 3 | a0001c0001t0007g0329 a0001c0001t0008g0111 a0001c0001t0026g0328 |
3 | HG02109.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.393+2938G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405563 | |||||||
| chr6:20405574 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.393+2949C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405574 | |||||||
| chr6:20405606 | C | T | 1 | a0001c0001t0028g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.393+2981C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405606 | |||||||
| chr6:20405640 | T | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0072 others(3): Show |
7 | HG00741.hp1 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+3015T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405640 | |||||||
| chr6:20405916 | T | C | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393+3291T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20405916 | |||||||
| chr6:20406043 | TA | T | 4 | a0001c0001t0001g0072 a0001c0001t0008g0069 a0001c0001t0025g0071 others(1): Show |
4 | HG00741.hp1 HG02486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+3421delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20406043 | ||||||
| chr6:20406066 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.393+3441G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406066 | |||||||
| chr6:20406196 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.393+3571G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406196 | |||||||
| chr6:20406470 | T | C | 2 | a0001c0001t0002g0224 a0001c0001t0010g0225 |
2 | NA19068.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.393+3845T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406470 | |||||||
| chr6:20406502 | G | A | 3 | a0001c0001t0007g0329 a0001c0001t0008g0111 a0001c0001t0026g0328 |
3 | HG02109.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.393+3877G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406502 | |||||||
| chr6:20406708 | T | A | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+4083T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406708 | |||||||
| chr6:20406796 | T | C | 1 | a0001c0001t0028g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.393+4171T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406796 | |||||||
| chr6:20406831 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.393+4206T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406831 | |||||||
| chr6:20406834 | T | C | 1 | a0001c0001t0007g0322 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.393+4209T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406834 | |||||||
| chr6:20406910 | G | C | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393+4285G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20406910 | |||||||
| chr6:20407051 | G | A | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+4426G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407051 | |||||||
| chr6:20407264 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.393+4639C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407264 | |||||||
| chr6:20407278 | G | C | 1 | a0001c0001t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.393+4653G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407278 | |||||||
| chr6:20407310 | C | T | 1 | a0001c0001t0002g0300 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.393+4685C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407310 | |||||||
| chr6:20407393 | A | G | 17 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0079 others(14): Show |
18 | HG00642.hp2 HG01081.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.393+4768A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407393 | |||||||
| chr6:20407435 | A | G | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393+4810A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407435 | |||||||
| chr6:20407589 | T | C | 1 | a0001c0001t0003g0323 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.393+4964T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407589 | |||||||
| chr6:20407680 | T | C | 3 | a0001c0001t0001g0217 a0001c0001t0002g0153 a0001c0001t0006g0152 |
3 | HG00438.hp1 HG02040.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.393+5055T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407680 | |||||||
| chr6:20407691 | G | A | 6 | a0001c0001t0003g0319 a0001c0001t0003g0320 a0001c0001t0003g0323 others(3): Show |
7 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+5066G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20407691 | |||||||
| chr6:20408254 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.393+5629A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408254 | |||||||
| chr6:20408330 | AGT | A | 54 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(51): Show |
54 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.393+5707_393+5708d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20408330 | ||||||
| chr6:20408360 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0003g0001 a0001c0001t0003g0014 |
5 | HG01361.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+5735C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408360 | |||||||
| chr6:20408498 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.393+5873T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408498 | |||||||
| chr6:20408570 | A | G | 1 | a0004c0004t0007g0321 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.393+5945A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408570 | |||||||
| chr6:20408656 | A | G | 2 | a0001c0001t0001g0307 a0001c0001t0017g0306 |
2 | HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.393+6031A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408656 | |||||||
| chr6:20408688 | T | C | 60 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
60 | HG00140.hp2 HG00642.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.393+6063T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408688 | |||||||
| chr6:20408899 | T | C | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+6274T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408899 | |||||||
| chr6:20408912 | G | T | 1 | a0001c0001t0007g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.393+6287G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20408912 | |||||||
| chr6:20409003 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.393+6378A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409003 | |||||||
| chr6:20409201 | C | T | 1 | a0001c0001t0008g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.393+6576C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409201 | |||||||
| chr6:20409275 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0068 others(6): Show |
12 | HG00741.hp1 HG01361.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+6650G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409275 | |||||||
| chr6:20409531 | G | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0307 a0001c0001t0017g0306 |
3 | HG02965.hp1 HG03209.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.393+6906G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409531 | |||||||
| chr6:20409544 | A | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(205): Show |
212 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.393+6919A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409544 | |||||||
| chr6:20409551 | T | G | 3 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0007t0002g0232 |
3 | NA18950.hp2 NA18995.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.393+6926T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409551 | |||||||
| chr6:20409703 | C | G | 6 | a0001c0001t0003g0319 a0001c0001t0003g0320 a0001c0001t0003g0323 others(3): Show |
7 | HG02258.hp2 HG02630.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+7078C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409703 | |||||||
| chr6:20409806 | G | C | 1 | a0001c0001t0003g0323 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.393+7181G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409806 | |||||||
| chr6:20409920 | C | T | 1 | a0001c0001t0007g0109 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.393+7295C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20409920 | |||||||
| chr6:20410046 | G | C | 1 | a0006c0006t0002g0018 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.393+7421G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410046 | |||||||
| chr6:20410094 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0003g0001 a0001c0001t0003g0014 |
5 | HG01361.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+7469T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410094 | |||||||
| chr6:20410371 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0002g0153 a0001c0001t0006g0152 |
3 | HG00438.hp1 HG02040.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.393+7746C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410371 | |||||||
| chr6:20410537 | A | T | 2 | a0001c0001t0001g0063 a0006c0006t0002g0018 |
2 | HG00140.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.393+7912A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410537 | |||||||
| chr6:20410578 | C | G | 1 | a0001c0001t0018g0213 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.393+7953C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410578 | |||||||
| chr6:20410584 | G | A | 1 | a0001c0001t0003g0323 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.393+7959G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410584 | |||||||
| chr6:20410736 | A | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0061 a0001c0001t0001g0062 others(3): Show |
6 | HG00140.hp2 HG02683.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+8111A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410736 | |||||||
| chr6:20410776 | G | A | 3 | a0001c0001t0001g0013 a0001c0001t0003g0001 a0001c0001t0003g0014 |
5 | HG01361.hp2 HG02572.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+8151G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410776 | |||||||
| chr6:20410939 | T | G | 2 | a0001c0001t0001g0077 a0001c0001t0005g0078 |
2 | HG01243.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.393+8314T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20410939 | |||||||
| chr6:20411079 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.393+8454T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411079 | |||||||
| chr6:20411274 | T | C | 1 | a0001c0001t0001g0325 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.393+8649T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411274 | |||||||
| chr6:20411333 | C | T | 4 | a0002c0002t0001g0074 a0002c0002t0001g0075 a0002c0002t0001g0076 others(1): Show |
4 | HG01255.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+8708C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411333 | |||||||
| chr6:20411444 | C | T | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+8819C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411444 | |||||||
| chr6:20411455 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.393+8830G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411455 | |||||||
| chr6:20411482 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.393+8857G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411482 | |||||||
| chr6:20411524 | C | T | 4 | a0002c0002t0001g0074 a0002c0002t0001g0075 a0002c0002t0001g0076 others(1): Show |
4 | HG01255.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+8899C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411524 | |||||||
| chr6:20411579 | C | T | 1 | a0001c0001t0003g0320 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.393+8954C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411579 | |||||||
| chr6:20411676 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0060 a0001c0001t0002g0059 |
3 | HG03017.hp2 HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.393+9051C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411676 | |||||||
| chr6:20411708 | C | T | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+9083C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411708 | |||||||
| chr6:20411905 | G | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0142 a0001c0001t0001g0143 others(2): Show |
5 | HG00323.hp2 HG01106.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+9280G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20411905 | |||||||
| chr6:20412019 | A | G | 1 | a0001c0001t0004g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.393+9394A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412019 | |||||||
| chr6:20412109 | T | G | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
9 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.393+9484T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412109 | |||||||
| chr6:20412321 | C | T | 3 | a0001c0001t0007g0329 a0001c0001t0008g0111 a0001c0001t0026g0328 |
3 | HG02109.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.393+9696C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412321 | |||||||
| chr6:20412541 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.393+9916C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412541 | |||||||
| chr6:20412616 | T | G | 3 | a0001c0001t0001g0126 a0001c0001t0003g0124 a0001c0001t0003g0127 |
3 | HG02896.hp2 HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.393+9991T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412616 | |||||||
| chr6:20412908 | G | A | 4 | a0001c0001t0003g0323 a0001c0001t0007g0322 a0004c0004t0001g0006 others(1): Show |
5 | HG02630.hp1 HG02717.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+10283G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20412908 | |||||||
| chr6:20413139 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0005g0078 a0001c0001t0005g0212 |
3 | HG01109.hp2 HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.393+10514A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413139 | |||||||
| chr6:20413286 | C | CAG | 31 | a0001c0001t0001g0010 a0001c0001t0001g0093 a0001c0001t0001g0094 others(28): Show |
31 | HG01109.hp1 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.393+10663_393+1066 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20413286 | ||||||
| chr6:20413354 | T | G | 1 | a0001c0001t0007g0322 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.393+10729T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413354 | |||||||
| chr6:20413369 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.393+10744C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413369 | |||||||
| chr6:20413490 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(222): Show |
230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.393+10865A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413490 | |||||||
| chr6:20413586 | G | A | 1 | a0001c0001t0002g0156 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.393+10961G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413586 | |||||||
| chr6:20413586 | G | T | 73 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(70): Show |
74 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.393+10961G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413586 | |||||||
| chr6:20413645 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.393+11020G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413645 | |||||||
| chr6:20413655 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG01167.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.393+11030G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413655 | |||||||
| chr6:20413855 | C | T | 4 | a0002c0002t0001g0074 a0002c0002t0001g0075 a0002c0002t0001g0076 others(1): Show |
4 | HG01255.hp1 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+11230C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413855 | |||||||
| chr6:20413870 | G | T | 4 | a0001c0001t0001g0292 a0001c0001t0001g0305 a0001c0001t0005g0293 others(1): Show |
4 | HG01175.hp2 HG01192.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+11245G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20413870 | |||||||
| chr6:20414008 | A | G | 3 | a0001c0001t0007g0329 a0001c0001t0008g0111 a0001c0001t0026g0328 |
3 | HG02109.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.393+11383A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414008 | |||||||
| chr6:20414058 | A | G | 2 | a0001c0001t0003g0319 a0001c0001t0003g0320 |
2 | HG02258.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.393+11433A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414058 | |||||||
| chr6:20414071 | G | C | 1 | a0001c0001t0002g0301 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.393+11446G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414071 | |||||||
| chr6:20414109 | T | C | 60 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(57): Show |
60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.393+11484T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414109 | |||||||
| chr6:20414223 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0005g0290 |
2 | HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.393+11598A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414223 | |||||||
| chr6:20414455 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(122): Show |
128 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.393+11830A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414455 | |||||||
| chr6:20414479 | A | G | 1 | a0001c0001t0001g0289 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.393+11854A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414479 | |||||||
| chr6:20414497 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.393+11872A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414497 | |||||||
| chr6:20414567 | C | T | 78 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0214 others(75): Show |
78 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.393+11942C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414567 | |||||||
| chr6:20414589 | A | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(119): Show |
125 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.393+11964A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414589 | |||||||
| chr6:20414663 | T | C | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393+12038T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414663 | |||||||
| chr6:20414774 | C | T | 70 | a0001c0001t0001g0017 a0001c0001t0001g0056 a0001c0001t0001g0149 others(67): Show |
71 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.393+12149C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414774 | |||||||
| chr6:20414822 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(207): Show |
214 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(211): Show |
intron_variant | MODIFIER | c.393+12197A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414822 | |||||||
| chr6:20414939 | A | G | 1 | a0001c0001t0004g0167 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.393+12314A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414939 | |||||||
| chr6:20414973 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.393+12348G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414973 | |||||||
| chr6:20414992 | A | G | 2 | a0001c0001t0001g0211 a0001c0001t0005g0288 |
2 | HG01175.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.393+12367A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20414992 | |||||||
| chr6:20415019 | C | T | 1 | a0001c0001t0003g0001 | 3 | HG03471.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.393+12394C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415019 | |||||||
| chr6:20415053 | A | G | 1 | a0001c0001t0004g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.393+12428A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415053 | |||||||
| chr6:20415074 | G | A | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG00408.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.393+12449G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415074 | |||||||
| chr6:20415395 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0072 others(28): Show |
34 | HG00741.hp1 HG01255.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.393+12770C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415395 | |||||||
| chr6:20415405 | A | G | 7 | a0001c0001t0003g0086 a0001c0001t0003g0087 a0001c0001t0003g0108 others(4): Show |
7 | HG01255.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.393+12780A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415405 | |||||||
| chr6:20415463 | A | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0072 a0001c0001t0001g0080 others(18): Show |
21 | HG00741.hp1 HG01361.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.393+12838A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415463 | |||||||
| chr6:20415637 | T | C | 1 | a0001c0001t0003g0122 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.393+13012T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415637 | |||||||
| chr6:20415665 | G | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+13040G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415665 | |||||||
| chr6:20415695 | A | G | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG00140.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+13070A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415695 | |||||||
| chr6:20415883 | A | G | 5 | a0001c0001t0001g0107 a0001c0001t0003g0086 a0001c0001t0003g0087 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+13258A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20415883 | |||||||
| chr6:20416084 | G | T | 1 | a0001c0001t0007g0322 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.393+13459G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416084 | |||||||
| chr6:20416119 | C | T | 111 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0049 others(108): Show |
115 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.393+13494C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416119 | |||||||
| chr6:20416182 | G | C | 1 | a0001c0001t0008g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.393+13557G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416182 | |||||||
| chr6:20416264 | A | G | 1 | a0001c0001t0008g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.393+13639A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416264 | |||||||
| chr6:20416289 | G | C | 1 | a0004c0004t0001g0006 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.393+13664G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416289 | |||||||
| chr6:20416341 | G | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(123): Show |
131 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.393+13716G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416341 | |||||||
| chr6:20416638 | C | T | 1 | a0001c0001t0003g0108 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.393+14013C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416638 | |||||||
| chr6:20416670 | C | T | 8 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(5): Show |
8 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+14045C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416670 | |||||||
| chr6:20416913 | G | A | 2 | a0001c0001t0023g0137 a0004c0004t0007g0321 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+14288G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416913 | |||||||
| chr6:20416961 | C | T | 67 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0041 others(64): Show |
68 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.393+14336C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20416961 | |||||||
| chr6:20417067 | C | A | 8 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0188 others(5): Show |
8 | NA18943.hp1 NA18950.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+14442C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20417067 | |||||||
| chr6:20417368 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.393+14743C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20417368 | |||||||
| chr6:20417588 | TA | T | 10 | a0001c0001t0001g0038 a0001c0001t0001g0210 a0001c0001t0001g0287 others(7): Show |
10 | HG01069.hp2 HG02280.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.393+14978delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20417588 | ||||||
| chr6:20417588 | TAA | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0061 others(23): Show |
30 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.393+14977_393+1497 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20417588 | ||||||
| chr6:20417588 | TAAAA | T | 8 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(5): Show |
8 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+14975_393+1497 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20417588 | ||||||
| chr6:20417745 | G | T | 81 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.393+15120G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20417745 | |||||||
| chr6:20417755 | C | T | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.393+15130C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20417755 | |||||||
| chr6:20417930 | C | G | 1 | a0001c0001t0001g0017 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.393+15305C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20417930 | |||||||
| chr6:20418098 | C | T | 51 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0041 others(48): Show |
52 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.393+15473C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20418098 | |||||||
| chr6:20418172 | C | G | 51 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0041 others(48): Show |
52 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.393+15547C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20418172 | |||||||
| chr6:20418177 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0079 others(10): Show |
13 | HG00741.hp1 HG01496.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.393+15552C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20418177 | |||||||
| chr6:20418487 | G | A | 7 | a0001c0001t0002g0024 a0001c0001t0002g0026 a0001c0001t0002g0027 others(4): Show |
7 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+15862G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20418487 | |||||||
| chr6:20418678 | AATGATCC others(1): Show |
A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0125 others(9): Show |
12 | HG00741.hp1 HG01496.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.393+16056_393+1606 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20418678 | ||||||
| chr6:20418749 | A | G | 2 | a0001c0001t0023g0137 a0004c0004t0007g0321 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+16124A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20418749 | |||||||
| chr6:20418840 | C | CT | 90 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0049 others(87): Show |
91 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.393+16226dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20418840 | ||||||
| chr6:20419078 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.393+16453C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419078 | |||||||
| chr6:20419104 | T | C | 6 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+16479T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419104 | |||||||
| chr6:20419270 | A | G | 91 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0049 others(88): Show |
92 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.393+16645A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419270 | |||||||
| chr6:20419334 | G | A | 1 | a0001c0001t0002g0193 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.393+16709G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419334 | |||||||
| chr6:20419428 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.393+16803C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419428 | |||||||
| chr6:20419529 | T | TTTTA | 4 | a0001c0001t0001g0317 a0001c0001t0004g0267 a0001c0001t0004g0268 others(1): Show |
4 | HG00099.hp2 HG02615.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+16929_393+1693 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20419529 | ||||||
| chr6:20419529 | TTTTA | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0061 others(56): Show |
63 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(60): Show |
intron_variant | MODIFIER | c.393+16929_393+1693 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20419529 | ||||||
| chr6:20419554 | T | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
18 | HG00741.hp1 HG01496.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.393+16929T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419554 | |||||||
| chr6:20419554 | TTTAC | T | 83 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0050 others(80): Show |
84 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.393+16949_393+1695 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20419554 | ||||||
| chr6:20419558 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0194 a0001c0001t0001g0195 others(3): Show |
6 | HG02074.hp1 HG03017.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+16933C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419558 | |||||||
| chr6:20419695 | AGCTGGAC others(11): Show |
A | 8 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(5): Show |
8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+17073_393+1709 others(22): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20419695 | ||||||
| chr6:20419720 | A | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(147): Show |
155 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.393+17095A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419720 | |||||||
| chr6:20419831 | G | C | 2 | a0001c0001t0001g0292 a0001c0001t0001g0305 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.393+17206G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419831 | |||||||
| chr6:20419892 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+17267G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20419892 | |||||||
| chr6:20420011 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(143): Show |
151 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.393+17386G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420011 | |||||||
| chr6:20420197 | T | C | 5 | a0001c0001t0001g0107 a0001c0001t0003g0086 a0001c0001t0003g0087 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+17572T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420197 | |||||||
| chr6:20420438 | G | GGT | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0183 others(3): Show |
6 | HG01109.hp1 HG01261.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+17838_393+1783 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20420438 | ||||||
| chr6:20420438 | GGT | G | 132 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(129): Show |
134 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.393+17838_393+1783 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20420438 | ||||||
| chr6:20420438 | GGTGT | G | 2 | a0001c0001t0001g0072 a0004c0004t0001g0006 |
3 | HG00741.hp1 HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.393+17836_393+1783 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20420438 | ||||||
| chr6:20420559 | C | T | 51 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0041 others(48): Show |
52 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(49): Show |
intron_variant | MODIFIER | c.393+17934C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420559 | |||||||
| chr6:20420775 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0077 |
3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+18150T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420775 | |||||||
| chr6:20420803 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+18178C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420803 | |||||||
| chr6:20420843 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.393+18218T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420843 | |||||||
| chr6:20420975 | A | C | 16 | a0001c0001t0001g0055 a0001c0001t0001g0207 a0001c0001t0001g0209 others(13): Show |
16 | NA18612.hp1 NA18950.hp2 NA18955.hp1 others(13): Show |
intron_variant | MODIFIER | c.393+18350A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20420975 | |||||||
| chr6:20421039 | G | A | 1 | a0003c0003t0001g0117 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.393+18414G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421039 | |||||||
| chr6:20421122 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+18497C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421122 | |||||||
| chr6:20421322 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.393+18697A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421322 | |||||||
| chr6:20421724 | C | T | 1 | a0001c0001t0003g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.393+19099C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421724 | |||||||
| chr6:20421776 | G | A | 1 | a0001c0001t0002g0226 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.393+19151G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421776 | |||||||
| chr6:20421787 | C | T | 5 | a0001c0001t0001g0107 a0001c0001t0003g0086 a0001c0001t0003g0087 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+19162C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421787 | |||||||
| chr6:20421879 | G | A | 2 | a0001c0001t0001g0072 a0001c0001t0005g0294 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.393+19254G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421879 | |||||||
| chr6:20421880 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+19255C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421880 | |||||||
| chr6:20421881 | G | A | 2 | a0001c0001t0001g0310 a0001c0001t0003g0309 |
2 | HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.393+19256G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421881 | |||||||
| chr6:20421918 | T | C | 2 | a0001c0001t0023g0137 a0004c0004t0007g0321 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+19293T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20421918 | |||||||
| chr6:20422348 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+19723T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422348 | |||||||
| chr6:20422448 | C | G | 2 | a0001c0001t0023g0137 a0004c0004t0007g0321 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+19823C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422448 | |||||||
| chr6:20422544 | G | C | 2 | a0001c0001t0023g0137 a0004c0004t0007g0321 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+19919G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422544 | |||||||
| chr6:20422546 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.393+19921C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422546 | |||||||
| chr6:20422580 | C | G | 2 | a0001c0001t0023g0137 a0004c0004t0007g0321 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+19955C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422580 | |||||||
| chr6:20422595 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(144): Show |
152 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.393+19970G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422595 | |||||||
| chr6:20422608 | T | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(146): Show |
154 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.393+19983T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422608 | |||||||
| chr6:20422638 | C | T | 8 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0249 others(5): Show |
8 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(5): Show |
intron_variant | MODIFIER | c.393+20013C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422638 | |||||||
| chr6:20422645 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.393+20020G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422645 | |||||||
| chr6:20422716 | G | A | 4 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+20091G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422716 | |||||||
| chr6:20422768 | A | G | 6 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(3): Show |
6 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+20143A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422768 | |||||||
| chr6:20422900 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0169 |
3 | HG01978.hp2 HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.393+20275C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422900 | |||||||
| chr6:20422996 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(144): Show |
152 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.393+20371G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20422996 | |||||||
| chr6:20423027 | C | T | 2 | a0001c0001t0023g0137 a0004c0004t0007g0321 |
2 | HG02717.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.393+20402C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423027 | |||||||
| chr6:20423029 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.393+20404A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423029 | |||||||
| chr6:20423108 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.393+20483C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423108 | |||||||
| chr6:20423385 | CT | C | 49 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0041 others(46): Show |
50 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.393+20762delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20423385 | ||||||
| chr6:20423463 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.393+20838T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423463 | |||||||
| chr6:20423545 | A | T | 3 | a0001c0001t0002g0037 a0001c0001t0002g0228 a0001c0001t0002g0229 |
3 | NA18953.hp1 NA18957.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.393+20920A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423545 | |||||||
| chr6:20423574 | G | A | 1 | a0004c0004t0001g0006 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.393+20949G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423574 | |||||||
| chr6:20423690 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.393+21065C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423690 | |||||||
| chr6:20423691 | G | A | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+21066G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423691 | |||||||
| chr6:20423713 | C | T | 49 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0041 others(46): Show |
50 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.393+21088C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423713 | |||||||
| chr6:20423764 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.393+21139C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423764 | |||||||
| chr6:20423765 | G | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+21140G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20423765 | |||||||
| chr6:20424064 | A | G | 2 | a0001c0001t0003g0008 a0001c0001t0003g0009 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.393+21439A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424064 | |||||||
| chr6:20424210 | G | GGT | 67 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(64): Show |
67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.393+21624_393+2162 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTATGT | 11 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0089 others(8): Show |
11 | HG01168.hp1 HG01496.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTATGTG others(1): Show |
12 | a0001c0001t0001g0107 a0001c0001t0001g0150 a0001c0001t0001g0215 others(9): Show |
12 | HG01255.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTATGTG others(3): Show |
22 | a0001c0001t0001g0010 a0001c0001t0001g0063 a0001c0001t0001g0119 others(19): Show |
22 | HG00438.hp1 HG00597.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTATGTG others(5): Show |
43 | a0001c0001t0001g0052 a0001c0001t0001g0055 a0001c0001t0001g0064 others(40): Show |
45 | HG00140.hp1 HG00544.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(16): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTATGTG others(7): Show |
34 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0050 others(31): Show |
35 | HG00408.hp2 HG01109.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(18): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTATGTG others(9): Show |
12 | a0001c0001t0001g0186 a0001c0001t0001g0195 a0001c0001t0001g0281 others(9): Show |
12 | HG02129.hp1 HG02145.hp2 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.393+21587_393+2158 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTATGTG others(11): Show |
2 | a0001c0001t0001g0194 a0001c0001t0002g0193 |
2 | HG00597.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.393+21587_393+2158 others(22): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTGT | 18 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0040 others(15): Show |
18 | HG00738.hp1 HG01167.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.393+21622_393+2162 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTGTGT | 37 | a0001c0001t0001g0038 a0001c0001t0001g0067 a0001c0001t0001g0113 others(34): Show |
38 | HG00280.hp2 HG00323.hp1 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.393+21620_393+2162 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTGTGTG others(1): Show |
5 | a0001c0001t0001g0019 a0001c0001t0001g0220 a0001c0001t0001g0266 others(2): Show |
5 | HG00741.hp2 HG02257.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+21618_393+2162 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0054 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.393+21616_393+2162 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | GGT | G | 5 | a0001c0001t0001g0079 a0001c0001t0001g0101 a0001c0001t0002g0057 others(2): Show |
6 | HG02572.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.393+21624_393+2162 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | GGTGT | G | 12 | a0001c0001t0001g0023 a0001c0001t0001g0061 a0001c0001t0001g0062 others(9): Show |
12 | HG01081.hp1 HG01243.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+21622_393+2162 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424210 | GGTGTGT | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+21620_393+2162 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424210 | ||||||
| chr6:20424212 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.393+21587T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424212 | |||||||
| chr6:20424213 | G | A | 7 | a0001c0001t0001g0072 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00741.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.393+21588G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424213 | |||||||
| chr6:20424215 | G | A | 2 | a0001c0001t0001g0079 a0004c0004t0001g0006 |
3 | HG02630.hp1 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.393+21590G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424215 | |||||||
| chr6:20424217 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0077 |
3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+21592G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424217 | |||||||
| chr6:20424219 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+21594G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424219 | |||||||
| chr6:20424250 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0118 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.393+21625_393+2162 others(15): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424250 | |||||||
| chr6:20424250 | T | TGTGTGTG others(8): Show |
3 | a0001c0001t0001g0120 a0001c0001t0001g0271 a0001c0001t0002g0198 |
3 | HG02055.hp1 HG03927.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.393+21625_393+2162 others(19): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424250 | |||||||
| chr6:20424331 | C | T | 1 | a0001c0001t0002g0300 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.393+21706C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424331 | |||||||
| chr6:20424383 | ATG | A | 161 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0013 others(158): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.393+21784_393+2178 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424383 | ||||||
| chr6:20424383 | ATGTG | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0101 others(8): Show |
12 | HG00280.hp1 HG01516.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.393+21782_393+2178 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424383 | ||||||
| chr6:20424383 | ATGTGTG | A | 143 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0049 others(140): Show |
147 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.393+21780_393+2178 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424383 | ||||||
| chr6:20424383 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0002g0156 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.393+21776_393+2178 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424383 | ||||||
| chr6:20424508 | T | A | 3 | a0001c0001t0001g0281 a0001c0001t0001g0283 a0001c0001t0002g0282 |
3 | NA18990.hp1 NA19009.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.393+21883T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424508 | |||||||
| chr6:20424588 | C | T | 49 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0041 others(46): Show |
50 | HG00544.hp2 HG00741.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.393+21963C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424588 | |||||||
| chr6:20424590 | T | C | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+21965T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424590 | |||||||
| chr6:20424592 | CT | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(144): Show |
152 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.393+21977delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424592 | ||||||
| chr6:20424613 | A | G | 4 | a0001c0001t0001g0140 a0001c0001t0001g0318 a0001c0001t0002g0233 others(1): Show |
4 | HG00280.hp1 HG00323.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+21988A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424613 | |||||||
| chr6:20424657 | T | C | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+22032T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424657 | |||||||
| chr6:20424694 | G | GA | 20 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0084 others(17): Show |
21 | HG01255.hp1 HG02055.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.393+22077dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20424694 | ||||||
| chr6:20424833 | G | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(149): Show |
157 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.393+22208G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424833 | |||||||
| chr6:20424887 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0007g0098 |
3 | HG02559.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.393+22262A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424887 | |||||||
| chr6:20424889 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.393+22264G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424889 | |||||||
| chr6:20424906 | A | G | 1 | a0001c0001t0002g0246 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.393+22281A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424906 | |||||||
| chr6:20424917 | A | G | 8 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(5): Show |
8 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+22292A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20424917 | |||||||
| chr6:20425227 | G | A | 202 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(199): Show |
208 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.393+22602G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425227 | |||||||
| chr6:20425365 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(143): Show |
151 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.393+22740G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425365 | |||||||
| chr6:20425387 | C | CT | 29 | a0001c0001t0001g0010 a0001c0001t0001g0046 a0001c0001t0001g0051 others(26): Show |
29 | HG00099.hp2 HG00140.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.393+22781dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20425387 | ||||||
| chr6:20425447 | G | A | 1 | a0001c0001t0013g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.393+22822G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425447 | |||||||
| chr6:20425510 | G | T | 312 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(309): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.393+22885G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425510 | |||||||
| chr6:20425593 | C | T | 2 | a0001c0001t0007g0109 a0004c0004t0007g0321 |
2 | HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.393+22968C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425593 | |||||||
| chr6:20425725 | C | G | 4 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0305 others(1): Show |
4 | HG01071.hp2 HG01192.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+23100C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425725 | |||||||
| chr6:20425836 | A | G | 2 | a0001c0001t0001g0252 a0001c0001t0005g0293 |
2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.393+23211A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425836 | |||||||
| chr6:20425940 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.393+23315T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20425940 | |||||||
| chr6:20426093 | A | C | 2 | a0001c0001t0002g0190 a0001c0001t0015g0192 |
2 | NA18990.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.393+23468A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426093 | |||||||
| chr6:20426504 | G | A | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+23879G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426504 | |||||||
| chr6:20426524 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.393+23899G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426524 | |||||||
| chr6:20426547 | CT | C | 260 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(257): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.393+23924delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20426547 | ||||||
| chr6:20426647 | G | A | 267 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(264): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.393+24022G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426647 | |||||||
| chr6:20426757 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.393+24132T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426757 | |||||||
| chr6:20426898 | T | A | 1 | a0001c0001t0001g0284 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.393+24273T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426898 | |||||||
| chr6:20426969 | A | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0254 |
2 | NA18948.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.393+24344A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426969 | |||||||
| chr6:20426998 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.393+24373C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20426998 | |||||||
| chr6:20427148 | C | A | 1 | a0004c0004t0001g0006 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.393+24523C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427148 | |||||||
| chr6:20427158 | T | G | 1 | a0001c0001t0002g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.393+24533T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427158 | |||||||
| chr6:20427238 | A | G | 272 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(269): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.393+24613A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427238 | |||||||
| chr6:20427260 | C | G | 266 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(263): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.393+24635C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427260 | |||||||
| chr6:20427308 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.393+24683A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427308 | |||||||
| chr6:20427477 | G | A | 2 | a0001c0001t0008g0111 a0001c0001t0025g0071 |
2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.393+24852G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427477 | |||||||
| chr6:20427604 | T | G | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+24979T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427604 | |||||||
| chr6:20427669 | C | T | 88 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0050 others(85): Show |
89 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.393+25044C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427669 | |||||||
| chr6:20427763 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.393+25138A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427763 | |||||||
| chr6:20427851 | G | A | 1 | a0001c0001t0008g0003 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.393+25226G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427851 | |||||||
| chr6:20427953 | C | T | 235 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(232): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.393+25328C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427953 | |||||||
| chr6:20427965 | A | G | 1 | a0001c0001t0005g0078 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.393+25340A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20427965 | |||||||
| chr6:20428201 | C | A | 86 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0028 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.393+25576C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428201 | |||||||
| chr6:20428228 | T | A | 5 | a0001c0001t0003g0108 a0002c0002t0001g0074 a0002c0002t0001g0075 others(2): Show |
5 | HG01255.hp1 HG02723.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+25603T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428228 | |||||||
| chr6:20428290 | C | A | 1 | a0001c0001t0003g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.393+25665C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428290 | |||||||
| chr6:20428354 | G | C | 51 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0040 others(48): Show |
52 | HG00544.hp2 HG00741.hp2 HG01069.hp2 others(49): Show |
intron_variant | MODIFIER | c.393+25729G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428354 | |||||||
| chr6:20428411 | C | T | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0079 others(19): Show |
22 | HG01255.hp2 HG02896.hp2 HG02965.hp1 others(19): Show |
intron_variant | MODIFIER | c.393+25786C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428411 | |||||||
| chr6:20428471 | C | T | 1 | a0001c0001t0011g0247 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.393+25846C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428471 | |||||||
| chr6:20428550 | G | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(264): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.393+25925G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428550 | |||||||
| chr6:20428686 | G | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+26061G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20428686 | |||||||
| chr6:20429171 | G | A | 1 | a0001c0001t0003g0319 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.393+26546G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429171 | |||||||
| chr6:20429288 | G | A | 1 | a0001c0001t0002g0223 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.393+26663G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429288 | |||||||
| chr6:20429369 | G | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0062 others(32): Show |
39 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(36): Show |
intron_variant | MODIFIER | c.393+26744G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429369 | |||||||
| chr6:20429452 | C | G | 11 | a0001c0001t0001g0116 a0001c0001t0003g0001 a0001c0001t0003g0127 others(8): Show |
13 | HG02109.hp1 HG02451.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.393+26827C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429452 | |||||||
| chr6:20429573 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.393+26948C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429573 | |||||||
| chr6:20429573 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0005g0293 |
2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.393+26948C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429573 | |||||||
| chr6:20429623 | A | G | 1 | a0001c0001t0004g0238 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.393+26998A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429623 | |||||||
| chr6:20429654 | A | G | 6 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+27029A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429654 | |||||||
| chr6:20429813 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.393+27188T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20429813 | |||||||
| chr6:20430084 | CT | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+27460delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430084 | |||||||
| chr6:20430373 | C | T | 23 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(20): Show |
23 | HG01255.hp1 HG02109.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.393+27748C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430373 | |||||||
| chr6:20430374 | G | A | 1 | a0001c0001t0016g0219 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.393+27749G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430374 | |||||||
| chr6:20430558 | T | G | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+27933T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430558 | |||||||
| chr6:20430842 | T | C | 1 | a0001c0001t0002g0223 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.393+28217T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430842 | |||||||
| chr6:20430964 | G | T | 1 | a0001c0001t0002g0246 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.393+28339G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20430964 | |||||||
| chr6:20431192 | G | A | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+28567G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431192 | |||||||
| chr6:20431208 | C | T | 1 | a0003c0003t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.393+28583C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431208 | |||||||
| chr6:20431397 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0077 |
3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+28772G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431397 | |||||||
| chr6:20431423 | C | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0084 others(14): Show |
18 | HG01255.hp1 HG02258.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.393+28798C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431423 | |||||||
| chr6:20431424 | G | A | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+28799G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431424 | |||||||
| chr6:20431465 | T | G | 1 | a0001c0001t0001g0255 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.393+28840T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431465 | |||||||
| chr6:20431510 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0057 |
2 | HG00642.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.393+28885G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431510 | |||||||
| chr6:20431543 | C | A | 1 | a0001c0001t0001g0020 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.393+28918C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431543 | |||||||
| chr6:20431558 | G | A | 8 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(5): Show |
8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+28933G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431558 | |||||||
| chr6:20431565 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.393+28940G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431565 | |||||||
| chr6:20431834 | C | T | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+29209C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431834 | |||||||
| chr6:20431876 | A | T | 8 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0097 others(5): Show |
8 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+29251A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20431876 | |||||||
| chr6:20432005 | T | C | 231 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.393+29380T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432005 | |||||||
| chr6:20432081 | A | T | 1 | a0001c0001t0007g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.393+29456A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432081 | |||||||
| chr6:20432253 | A | C | 25 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(22): Show |
27 | HG01255.hp1 HG02109.hp1 HG02258.hp2 others(24): Show |
intron_variant | MODIFIER | c.393+29628A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432253 | |||||||
| chr6:20432253 | A | G | 240 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(237): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.393+29628A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432253 | |||||||
| chr6:20432273 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.393+29648G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432273 | |||||||
| chr6:20432313 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | NA19010.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.393+29688G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432313 | |||||||
| chr6:20432317 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.393+29692G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432317 | |||||||
| chr6:20432349 | C | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | HG03710.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.393+29724C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432349 | |||||||
| chr6:20432375 | A | G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0182 a0001c0001t0001g0214 others(1): Show |
4 | HG02083.hp2 NA18954.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+29750A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432375 | |||||||
| chr6:20432496 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.393+29871G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432496 | |||||||
| chr6:20432498 | G | A | 23 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(20): Show |
23 | HG01255.hp1 HG02109.hp1 HG02258.hp2 others(20): Show |
intron_variant | MODIFIER | c.393+29873G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432498 | |||||||
| chr6:20432621 | T | A | 1 | a0001c0001t0003g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.393+29996T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432621 | |||||||
| chr6:20432683 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.393+30058G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432683 | |||||||
| chr6:20432745 | C | T | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(6): Show |
9 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+30120C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432745 | |||||||
| chr6:20432759 | G | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+30134G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432759 | |||||||
| chr6:20432762 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.393+30137G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432762 | |||||||
| chr6:20432846 | A | G | 288 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(285): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.393+30221A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20432846 | |||||||
| chr6:20433066 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.393+30441A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433066 | |||||||
| chr6:20433153 | T | A | 15 | a0001c0001t0001g0116 a0001c0001t0003g0014 a0001c0001t0003g0108 others(12): Show |
15 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.393+30528T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433153 | |||||||
| chr6:20433406 | C | G | 1 | a0001c0001t0005g0288 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.393+30781C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433406 | |||||||
| chr6:20433617 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+30992G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433617 | |||||||
| chr6:20433646 | CAGA | C | 8 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(5): Show |
8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+31026_393+3102 others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20433646 | ||||||
| chr6:20433736 | A | C | 15 | a0001c0001t0001g0055 a0001c0001t0001g0207 a0001c0001t0001g0209 others(12): Show |
15 | NA18612.hp1 NA18950.hp2 NA18955.hp1 others(12): Show |
intron_variant | MODIFIER | c.393+31111A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433736 | |||||||
| chr6:20433835 | C | T | 8 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(5): Show |
8 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+31210C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433835 | |||||||
| chr6:20433935 | T | C | 1 | a0003c0003t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.393+31310T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20433935 | |||||||
| chr6:20434162 | T | G | 1 | a0001c0001t0001g0327 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.393+31537T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434162 | |||||||
| chr6:20434344 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0077 |
3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+31719G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434344 | |||||||
| chr6:20434636 | T | C | 16 | a0001c0001t0001g0097 a0001c0001t0001g0116 a0001c0001t0003g0014 others(13): Show |
16 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.393+32011T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434636 | |||||||
| chr6:20434727 | C | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02257.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+32102C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434727 | |||||||
| chr6:20434732 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+32107C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434732 | |||||||
| chr6:20434888 | C | T | 1 | a0001c0001t0005g0290 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.393+32263C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20434888 | |||||||
| chr6:20435025 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.393+32400T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435025 | |||||||
| chr6:20435073 | AGAATATT others(4): Show |
A | 2 | a0001c0001t0003g0008 a0001c0001t0003g0009 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.393+32450_393+3246 others(15): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20435073 | ||||||
| chr6:20435083 | A | T | 1 | a0003c0003t0001g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.393+32458A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435083 | |||||||
| chr6:20435090 | G | C | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+32465G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435090 | |||||||
| chr6:20435189 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.393+32564C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435189 | |||||||
| chr6:20435322 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.393+32697A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435322 | |||||||
| chr6:20435371 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.393+32746C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435371 | |||||||
| chr6:20435441 | A | G | 1 | a0002c0002t0001g0076 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.393+32816A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435441 | |||||||
| chr6:20435623 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.393+32998C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20435623 | |||||||
| chr6:20435974 | C | CT | 7 | a0001c0001t0001g0094 a0001c0001t0001g0096 a0001c0001t0002g0158 others(4): Show |
7 | HG02145.hp2 HG02717.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.393+33371dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20435974 | ||||||
| chr6:20435974 | CT | C | 27 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0093 others(24): Show |
30 | HG00642.hp2 HG01081.hp2 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.393+33371delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20435974 | ||||||
| chr6:20435974 | CTTTTTTT others(4): Show |
C | 226 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.393+33361_393+3337 others(15): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20435974 | ||||||
| chr6:20436006 | A | G | 1 | a0001c0001t0025g0071 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.393+33381A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436006 | |||||||
| chr6:20436022 | C | G | 9 | a0001c0001t0001g0097 a0001c0001t0001g0116 a0001c0001t0003g0127 others(6): Show |
9 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+33397C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436022 | |||||||
| chr6:20436043 | T | C | 251 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(248): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.393+33418T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436043 | |||||||
| chr6:20436137 | C | T | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(6): Show |
9 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+33512C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436137 | |||||||
| chr6:20436208 | T | C | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+33583T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436208 | |||||||
| chr6:20436260 | C | T | 7 | a0001c0001t0003g0014 a0001c0001t0003g0108 a0002c0002t0001g0074 others(4): Show |
7 | HG01255.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.393+33635C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436260 | |||||||
| chr6:20436304 | G | C | 8 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(5): Show |
8 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+33679G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436304 | |||||||
| chr6:20436307 | A | G | 4 | a0001c0001t0001g0287 a0001c0001t0002g0230 a0001c0001t0002g0231 others(1): Show |
4 | NA18950.hp2 NA18995.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+33682A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436307 | |||||||
| chr6:20436421 | A | C | 226 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.393+33796A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436421 | |||||||
| chr6:20436452 | A | AAC | 10 | a0001c0001t0001g0066 a0001c0001t0001g0092 a0001c0001t0001g0128 others(7): Show |
10 | HG01175.hp1 HG02055.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.393+33853_393+3385 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | ||||||
| chr6:20436452 | A | AACAC | 3 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0005g0293 |
3 | HG01175.hp2 NA19010.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.393+33851_393+3385 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | ||||||
| chr6:20436452 | A | AACACACA others(5): Show |
1 | a0002c0002t0001g0075 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.393+33843_393+3385 others(16): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | ||||||
| chr6:20436452 | A | AACACACA others(7): Show |
5 | a0001c0001t0003g0014 a0001c0001t0003g0108 a0002c0002t0001g0076 others(2): Show |
5 | HG01255.hp1 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+33841_393+3385 others(18): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | ||||||
| chr6:20436452 | A | AACACACA others(9): Show |
1 | a0002c0002t0001g0074 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.393+33839_393+3385 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | ||||||
| chr6:20436452 | AAC | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0061 others(18): Show |
23 | HG01243.hp2 HG01358.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.393+33853_393+3385 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | ||||||
| chr6:20436452 | AACAC | A | 14 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0085 others(11): Show |
14 | HG00741.hp1 HG02109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.393+33851_393+3385 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436452 | ||||||
| chr6:20436464 | CACACACA others(9): Show |
C | 1 | a0001c0001t0001g0097 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.393+33841_393+3385 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436464 | ||||||
| chr6:20436476 | C | G | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0077 |
3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.393+33851C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436476 | |||||||
| chr6:20436476 | CACAG | C | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+33853_393+3385 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436476 | ||||||
| chr6:20436476 | CACAGAGA others(3): Show |
C | 1 | a0001c0001t0008g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.393+33853_393+3386 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436476 | ||||||
| chr6:20436478 | C | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0061 others(31): Show |
37 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.393+33853C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436478 | |||||||
| chr6:20436478 | CAG | C | 5 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0118 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+33869_393+3387 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436478 | ||||||
| chr6:20436478 | CAGAGAG | C | 5 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(2): Show |
5 | HG02965.hp2 HG03098.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+33865_393+3387 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436478 | ||||||
| chr6:20436478 | CAGAGAGA others(3): Show |
C | 1 | a0001c0001t0025g0071 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.393+33861_393+3387 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436478 | ||||||
| chr6:20436480 | G | C | 112 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(109): Show |
112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.393+33855G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436480 | |||||||
| chr6:20436482 | G | C | 11 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(8): Show |
11 | HG01167.hp2 HG01255.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.393+33857G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436482 | |||||||
| chr6:20436484 | G | C | 1 | a0001c0001t0026g0328 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.393+33859G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436484 | |||||||
| chr6:20436486 | G | C | 6 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(3): Show |
6 | HG02451.hp2 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+33861G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436486 | |||||||
| chr6:20436488 | G | C | 6 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(3): Show |
6 | HG02451.hp2 HG02965.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+33863G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436488 | |||||||
| chr6:20436494 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0135 others(9): Show |
13 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.393+33869G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436494 | |||||||
| chr6:20436494 | GAA | G | 126 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0038 others(123): Show |
128 | HG00140.hp1 HG00408.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.393+33873_393+3387 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20436494 | ||||||
| chr6:20436496 | A | G | 100 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(97): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.393+33871A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436496 | |||||||
| chr6:20436508 | C | T | 15 | a0001c0001t0001g0116 a0001c0001t0003g0014 a0001c0001t0003g0108 others(12): Show |
15 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.393+33883C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436508 | |||||||
| chr6:20436615 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.393+33990C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436615 | |||||||
| chr6:20436623 | C | T | 8 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(5): Show |
8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+33998C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436623 | |||||||
| chr6:20436718 | C | T | 15 | a0001c0001t0001g0116 a0001c0001t0003g0014 a0001c0001t0003g0108 others(12): Show |
15 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.393+34093C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436718 | |||||||
| chr6:20436823 | C | T | 9 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0042 others(6): Show |
9 | HG01069.hp2 HG01261.hp2 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+34198C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436823 | |||||||
| chr6:20436956 | C | T | 3 | a0001c0001t0001g0097 a0001c0001t0003g0001 a0001c0001t0021g0104 |
5 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+34331C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20436956 | |||||||
| chr6:20437182 | T | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0201 |
2 | HG01943.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.393+34557T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20437182 | |||||||
| chr6:20437383 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.393+34758G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20437383 | |||||||
| chr6:20437480 | CT | C | 14 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(11): Show |
14 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.393+34865delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20437480 | ||||||
| chr6:20437534 | T | C | 85 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(82): Show |
86 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.393+34909T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20437534 | |||||||
| chr6:20437726 | G | A | 7 | a0001c0001t0003g0014 a0001c0001t0003g0108 a0002c0002t0001g0074 others(4): Show |
7 | HG01255.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.393+35101G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20437726 | |||||||
| chr6:20437898 | T | A | 15 | a0001c0001t0001g0116 a0001c0001t0003g0014 a0001c0001t0003g0108 others(12): Show |
15 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.393+35273T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20437898 | |||||||
| chr6:20438110 | A | AC | 15 | a0001c0001t0001g0116 a0001c0001t0003g0014 a0001c0001t0003g0108 others(12): Show |
15 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.393+35485_393+3548 others(5): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438110 | |||||||
| chr6:20438190 | C | T | 3 | a0001c0001t0001g0097 a0001c0001t0003g0001 a0001c0001t0021g0104 |
5 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+35565C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438190 | |||||||
| chr6:20438201 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0266 |
2 | NA18981.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.393+35576G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438201 | |||||||
| chr6:20438412 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.393+35787C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438412 | |||||||
| chr6:20438430 | C | T | 281 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(278): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.393+35805C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438430 | |||||||
| chr6:20438549 | G | A | 1 | a0001c0001t0005g0288 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.393+35924G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438549 | |||||||
| chr6:20438615 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.393+35990C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438615 | |||||||
| chr6:20438635 | C | G | 5 | a0001c0001t0001g0107 a0001c0001t0003g0086 a0001c0001t0003g0087 others(2): Show |
5 | HG02109.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.393+36010C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438635 | |||||||
| chr6:20438731 | A | G | 5 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0007g0109 others(2): Show |
5 | HG02145.hp2 HG02280.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.393+36106A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20438731 | |||||||
| chr6:20439049 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.393+36424A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439049 | |||||||
| chr6:20439097 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0068 others(10): Show |
14 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.393+36472A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439097 | |||||||
| chr6:20439201 | AT | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG01167.hp2 HG02145.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.393+36582delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20439201 | ||||||
| chr6:20439226 | T | C | 8 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(5): Show |
8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+36601T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439226 | |||||||
| chr6:20439229 | A | G | 4 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.393+36604A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439229 | |||||||
| chr6:20439266 | A | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0135 others(3): Show |
6 | HG01496.hp1 HG02258.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.393+36641A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439266 | |||||||
| chr6:20439278 | T | G | 3 | a0001c0001t0001g0253 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG02074.hp2 HG02080.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.393+36653T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439278 | |||||||
| chr6:20439334 | C | T | 9 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(6): Show |
9 | HG02258.hp2 HG02486.hp1 HG03516.hp2 others(6): Show |
intron_variant | MODIFIER | c.393+36709C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439334 | |||||||
| chr6:20439397 | G | A | 56 | a0001c0001t0001g0019 a0001c0001t0001g0038 a0001c0001t0001g0040 others(53): Show |
57 | HG00544.hp2 HG00741.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.393+36772G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439397 | |||||||
| chr6:20439592 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.393+36967C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439592 | |||||||
| chr6:20439711 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.393+37086T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439711 | |||||||
| chr6:20439907 | A | G | 1 | a0001c0001t0002g0184 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.393+37282A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439907 | |||||||
| chr6:20439922 | A | G | 1 | a0001c0001t0003g0323 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.393+37297A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439922 | |||||||
| chr6:20439951 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.393+37326C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439951 | |||||||
| chr6:20439981 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18953.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.393+37356G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439981 | |||||||
| chr6:20439998 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.393+37373C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20439998 | |||||||
| chr6:20440071 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0157 a0001c0001t0002g0158 |
3 | NA18968.hp2 NA19062.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.393+37446C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20440071 | |||||||
| chr6:20440303 | T | C | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.393+37678T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20440303 | |||||||
| chr6:20440352 | A | G | 8 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(5): Show |
8 | HG02109.hp1 HG02451.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.393+37727A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20440352 | |||||||
| chr6:20440404 | G | A | 1 | a0003c0003t0001g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.393+37779G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20440404 | |||||||
| chr6:20440602 | G | T | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.393+37977G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20440602 | |||||||
| chr6:20441112 | A | G | 1 | a0001c0001t0003g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.393+38487A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441112 | |||||||
| chr6:20441315 | T | C | 1 | a0001c0001t0001g0227 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.394-38531T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441315 | |||||||
| chr6:20441441 | T | G | 3 | a0001c0001t0002g0138 a0001c0001t0002g0176 a0001c0001t0002g0177 |
3 | HG02602.hp1 NA18980.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.394-38405T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441441 | |||||||
| chr6:20441541 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.394-38305C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441541 | |||||||
| chr6:20441570 | T | C | 2 | a0001c0001t0001g0270 a0001c0001t0001g0325 |
2 | NA18955.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.394-38276T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441570 | |||||||
| chr6:20441571 | G | GTGTTTT | 7 | a0001c0001t0001g0216 a0001c0001t0005g0004 a0001c0001t0005g0078 others(4): Show |
8 | HG01175.hp1 HG01192.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-38261_394-3825 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20441571 | ||||||
| chr6:20441725 | A | AT | 9 | a0001c0001t0001g0083 a0001c0001t0001g0253 a0001c0001t0001g0325 others(6): Show |
9 | HG01175.hp1 HG02074.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-38099dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20441725 | ||||||
| chr6:20441725 | AT | A | 145 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0017 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.394-38099delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20441725 | ||||||
| chr6:20441730 | T | A | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-38116T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441730 | |||||||
| chr6:20441735 | T | A | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-38111T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441735 | |||||||
| chr6:20441759 | C | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(279): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.394-38087C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441759 | |||||||
| chr6:20441830 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0068 others(10): Show |
14 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-38016C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441830 | |||||||
| chr6:20441857 | C | T | 226 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.394-37989C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20441857 | |||||||
| chr6:20441997 | C | CT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0068 others(21): Show |
26 | HG01496.hp1 HG02258.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-37836dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20441997 | ||||||
| chr6:20441997 | C | CTT | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(6): Show |
9 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-37837_394-3783 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20441997 | ||||||
| chr6:20442077 | C | A | 230 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(227): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.394-37769C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442077 | |||||||
| chr6:20442078 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-37768G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442078 | |||||||
| chr6:20442083 | T | G | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-37763T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442083 | |||||||
| chr6:20442123 | C | T | 177 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(174): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.394-37723C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442123 | |||||||
| chr6:20442259 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.394-37587C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442259 | |||||||
| chr6:20442599 | T | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0278 |
3 | NA18953.hp2 NA18971.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.394-37247T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442599 | |||||||
| chr6:20442623 | A | G | 236 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.394-37223A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442623 | |||||||
| chr6:20442693 | G | A | 1 | a0001c0001t0004g0053 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.394-37153G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442693 | |||||||
| chr6:20442798 | C | T | 1 | a0001c0001t0028g0110 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.394-37048C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442798 | |||||||
| chr6:20442867 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.394-36979G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442867 | |||||||
| chr6:20442920 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-36926A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442920 | |||||||
| chr6:20442967 | C | CA | 280 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(277): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.394-36866dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20442967 | ||||||
| chr6:20442980 | A | T | 2 | a0003c0003t0001g0070 a0003c0003t0001g0117 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-36866A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442980 | |||||||
| chr6:20442993 | T | G | 1 | a0001c0001t0003g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.394-36853T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20442993 | |||||||
| chr6:20443295 | A | C | 2 | a0001c0001t0003g0014 a0001c0001t0023g0137 |
2 | HG02572.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.394-36551A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443295 | |||||||
| chr6:20443319 | CAA | C | 52 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0038 others(49): Show |
53 | HG00544.hp2 HG00741.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.394-36524_394-3652 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20443319 | ||||||
| chr6:20443347 | C | T | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0118 others(3): Show |
6 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-36499C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443347 | |||||||
| chr6:20443451 | T | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0061 others(30): Show |
35 | HG00741.hp1 HG01243.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.394-36395T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443451 | |||||||
| chr6:20443602 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.394-36244G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443602 | |||||||
| chr6:20443693 | T | C | 1 | a0003c0003t0001g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-36153T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443693 | |||||||
| chr6:20443798 | A | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0068 others(10): Show |
14 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-36048A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443798 | |||||||
| chr6:20443951 | C | G | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(6): Show |
9 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-35895C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20443951 | |||||||
| chr6:20444176 | G | A | 236 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.394-35670G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444176 | |||||||
| chr6:20444193 | A | T | 2 | a0001c0001t0008g0111 a0001c0001t0025g0071 |
2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.394-35653A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444193 | |||||||
| chr6:20444211 | G | A | 3 | a0001c0001t0001g0237 a0005c0005t0001g0147 a0005c0005t0004g0178 |
3 | HG02129.hp2 HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.394-35635G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444211 | |||||||
| chr6:20444273 | A | T | 272 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(269): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.394-35573A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444273 | |||||||
| chr6:20444287 | A | G | 238 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.394-35559A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444287 | |||||||
| chr6:20444513 | C | T | 5 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0088 others(2): Show |
5 | HG02486.hp1 HG03516.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-35333C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444513 | |||||||
| chr6:20444694 | C | A | 14 | a0001c0001t0001g0116 a0001c0001t0003g0108 a0001c0001t0003g0127 others(11): Show |
14 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-35152C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20444694 | |||||||
| chr6:20444756 | AT | A | 41 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(38): Show |
44 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.394-35084delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20444756 | ||||||
| chr6:20445172 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-34674T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445172 | |||||||
| chr6:20445247 | C | CT | 12 | a0001c0001t0001g0116 a0001c0001t0003g0001 a0001c0001t0003g0127 others(9): Show |
14 | HG02109.hp1 HG02451.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-34587dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20445247 | ||||||
| chr6:20445247 | C | CTTT | 14 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(11): Show |
15 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.394-34589_394-3458 others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20445247 | ||||||
| chr6:20445455 | G | T | 1 | a0001c0001t0002g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-34391G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445455 | |||||||
| chr6:20445479 | C | T | 1 | a0003c0003t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.394-34367C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445479 | |||||||
| chr6:20445622 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.394-34224G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445622 | |||||||
| chr6:20445641 | G | A | 16 | a0001c0001t0001g0116 a0001c0001t0003g0001 a0001c0001t0003g0108 others(13): Show |
18 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.394-34205G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445641 | |||||||
| chr6:20445741 | A | G | 14 | a0001c0001t0001g0116 a0001c0001t0003g0108 a0001c0001t0003g0127 others(11): Show |
14 | HG01255.hp1 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-34105A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445741 | |||||||
| chr6:20445918 | G | C | 12 | a0001c0001t0001g0055 a0001c0001t0001g0270 a0001c0001t0001g0281 others(9): Show |
12 | NA18950.hp2 NA18955.hp1 NA18957.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-33928G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20445918 | |||||||
| chr6:20446215 | T | C | 4 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0007g0109 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-33631T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446215 | |||||||
| chr6:20446405 | A | G | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-33441A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446405 | |||||||
| chr6:20446470 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.394-33376T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446470 | |||||||
| chr6:20446503 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0256 |
2 | HG00741.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.394-33343A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446503 | |||||||
| chr6:20446795 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.394-33051G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446795 | |||||||
| chr6:20446802 | A | T | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-33044A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446802 | |||||||
| chr6:20446803 | G | T | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-33043G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446803 | |||||||
| chr6:20446827 | A | G | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-33019A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20446827 | |||||||
| chr6:20447017 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.394-32829C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447017 | |||||||
| chr6:20447062 | A | G | 323 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(320): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.394-32784A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447062 | |||||||
| chr6:20447069 | G | A | 10 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(7): Show |
11 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.394-32777G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447069 | |||||||
| chr6:20447119 | G | C | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-32727G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447119 | |||||||
| chr6:20447158 | G | A | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0118 others(3): Show |
6 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-32688G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447158 | |||||||
| chr6:20447268 | T | G | 1 | a0001c0001t0003g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.394-32578T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447268 | |||||||
| chr6:20447304 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.394-32542G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447304 | |||||||
| chr6:20447322 | A | ATG | 3 | a0001c0001t0001g0151 a0001c0001t0001g0269 a0001c0001t0027g0036 |
3 | HG03704.hp1 NA18997.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.394-32510_394-3250 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20447322 | ||||||
| chr6:20447373 | G | C | 2 | a0003c0003t0001g0070 a0003c0003t0001g0117 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-32473G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447373 | |||||||
| chr6:20447541 | C | CT | 16 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(13): Show |
17 | HG00741.hp1 HG01243.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.394-32293dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20447541 | ||||||
| chr6:20447541 | C | CTT | 6 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0118 others(3): Show |
6 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-32294_394-3229 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20447541 | ||||||
| chr6:20447554 | A | T | 1 | a0001c0001t0027g0036 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.394-32292A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447554 | |||||||
| chr6:20447632 | G | A | 287 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(284): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.394-32214G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447632 | |||||||
| chr6:20447996 | G | A | 1 | a0004c0004t0001g0006 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.394-31850G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20447996 | |||||||
| chr6:20448053 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-31793C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20448053 | |||||||
| chr6:20448386 | T | C | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-31460T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20448386 | |||||||
| chr6:20448464 | T | TAC | 6 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0175 others(3): Show |
6 | HG02055.hp1 HG02486.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-31364_394-3136 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20448464 | ||||||
| chr6:20448678 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.394-31168C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20448678 | |||||||
| chr6:20448927 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.394-30919A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20448927 | |||||||
| chr6:20449012 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.394-30834T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449012 | |||||||
| chr6:20449084 | C | T | 2 | a0001c0001t0008g0111 a0001c0001t0025g0071 |
2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.394-30762C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449084 | |||||||
| chr6:20449375 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.394-30471C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449375 | |||||||
| chr6:20449438 | C | T | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(5): Show |
8 | HG00741.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-30408C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449438 | |||||||
| chr6:20449673 | G | A | 87 | a0001c0001t0001g0017 a0001c0001t0001g0049 a0001c0001t0001g0050 others(84): Show |
88 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.394-30173G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449673 | |||||||
| chr6:20449731 | T | C | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(9): Show |
13 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-30115T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449731 | |||||||
| chr6:20449800 | C | G | 3 | a0001c0001t0003g0001 a0001c0001t0021g0104 a0001c0001t0025g0071 |
5 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-30046C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449800 | |||||||
| chr6:20449883 | G | A | 1 | a0001c0008t0001g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.394-29963G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449883 | |||||||
| chr6:20449891 | G | A | 1 | a0001c0001t0004g0058 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.394-29955G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449891 | |||||||
| chr6:20449959 | T | C | 2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-29887T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449959 | |||||||
| chr6:20449960 | T | TATGAGAT others(2): Show |
2 | a0001c0001t0003g0001 a0001c0001t0021g0104 |
4 | HG02615.hp2 HG03471.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-29886_394-2988 others(13): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449960 | |||||||
| chr6:20449985 | A | G | 294 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(291): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.394-29861A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20449985 | |||||||
| chr6:20450090 | A | C | 1 | a0001c0001t0008g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.394-29756A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450090 | |||||||
| chr6:20450120 | C | T | 1 | a0001c0001t0003g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.394-29726C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450120 | |||||||
| chr6:20450350 | G | C | 3 | a0001c0001t0002g0037 a0001c0001t0002g0228 a0001c0001t0002g0229 |
3 | NA18953.hp1 NA18957.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.394-29496G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450350 | |||||||
| chr6:20450438 | T | A | 4 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-29408T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450438 | |||||||
| chr6:20450461 | T | C | 4 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-29385T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450461 | |||||||
| chr6:20450640 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.394-29206T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450640 | |||||||
| chr6:20450751 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | NA18943.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.394-29095A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20450751 | |||||||
| chr6:20451231 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.394-28615G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20451231 | |||||||
| chr6:20451290 | T | A | 281 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(278): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.394-28556T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20451290 | |||||||
| chr6:20451335 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.394-28511A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20451335 | |||||||
| chr6:20451559 | C | T | 8 | a0001c0001t0006g0005 a0001c0001t0006g0039 a0001c0001t0006g0152 others(5): Show |
9 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-28287C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20451559 | |||||||
| chr6:20452041 | G | A | 1 | a0001c0001t0016g0219 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.394-27805G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452041 | |||||||
| chr6:20452260 | G | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0318 a0001c0001t0011g0247 |
3 | HG00323.hp2 HG01106.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.394-27586G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452260 | |||||||
| chr6:20452309 | C | A | 2 | a0003c0003t0001g0070 a0003c0003t0001g0117 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-27537C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452309 | |||||||
| chr6:20452467 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0128 |
2 | HG02055.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.394-27379C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452467 | |||||||
| chr6:20452504 | T | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(285): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.394-27342T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452504 | |||||||
| chr6:20452878 | C | T | 1 | a0004c0004t0001g0006 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.394-26968C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452878 | |||||||
| chr6:20452991 | TTTTG | T | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(268): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.394-26827_394-2682 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20452991 | ||||||
| chr6:20452991 | TTTTGTTT others(1): Show |
T | 17 | a0001c0001t0001g0051 a0001c0001t0001g0061 a0001c0001t0001g0062 others(14): Show |
20 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.394-26831_394-2682 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20452991 | ||||||
| chr6:20452997 | T | C | 11 | a0001c0001t0001g0067 a0001c0001t0001g0245 a0001c0001t0001g0254 others(8): Show |
12 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-26849T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452997 | |||||||
| chr6:20452999 | G | T | 11 | a0001c0001t0001g0067 a0001c0001t0001g0245 a0001c0001t0001g0254 others(8): Show |
12 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-26847G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20452999 | |||||||
| chr6:20453432 | GGA | G | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(9): Show |
14 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-26413_394-2641 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453432 | |||||||
| chr6:20453435 | A | T | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(9): Show |
14 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-26411A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453435 | |||||||
| chr6:20453436 | A | T | 12 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0072 others(9): Show |
14 | HG00741.hp1 HG01243.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.394-26410A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453436 | |||||||
| chr6:20453492 | G | A | 4 | a0001c0001t0001g0116 a0001c0001t0003g0127 a0001c0001t0003g0319 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-26354G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453492 | |||||||
| chr6:20453601 | G | A | 1 | a0001c0001t0008g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.394-26245G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453601 | |||||||
| chr6:20453602 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.394-26244A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453602 | |||||||
| chr6:20453608 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.394-26238C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453608 | |||||||
| chr6:20453649 | C | T | 1 | a0004c0004t0001g0006 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.394-26197C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453649 | |||||||
| chr6:20453854 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0008g0003 a0001c0001t0008g0081 |
4 | HG00642.hp2 HG01081.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-25992T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20453854 | |||||||
| chr6:20454143 | AACAGGAG others(21): Show |
A | 1 | a0001c0001t0001g0017 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.394-25702_394-2567 others(32): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454143 | |||||||
| chr6:20454233 | T | C | 5 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0155 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.394-25613T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454233 | |||||||
| chr6:20454369 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.394-25477C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454369 | |||||||
| chr6:20454543 | G | C | 5 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-25303G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454543 | |||||||
| chr6:20454637 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.394-25209A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454637 | |||||||
| chr6:20454653 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.394-25193T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454653 | |||||||
| chr6:20454779 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.394-25067C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454779 | |||||||
| chr6:20454861 | G | A | 3 | a0001c0001t0001g0312 a0001c0001t0003g0313 a0001c0001t0024g0308 |
3 | HG01884.hp1 HG03225.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.394-24985G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454861 | |||||||
| chr6:20454921 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.394-24925A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454921 | |||||||
| chr6:20454981 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.394-24865A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454981 | |||||||
| chr6:20454993 | T | C | 1 | a0003c0003t0001g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-24853T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20454993 | |||||||
| chr6:20455049 | G | A | 289 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(286): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.394-24797G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455049 | |||||||
| chr6:20455052 | C | T | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24794C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455052 | |||||||
| chr6:20455333 | C | T | 89 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0049 others(86): Show |
90 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.394-24513C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455333 | |||||||
| chr6:20455574 | A | C | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24272A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455574 | |||||||
| chr6:20455675 | G | T | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24171G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455675 | |||||||
| chr6:20455676 | G | T | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24170G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455676 | |||||||
| chr6:20455677 | C | T | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24169C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455677 | |||||||
| chr6:20455679 | C | T | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24167C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455679 | |||||||
| chr6:20455680 | T | TC | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24166_394-2416 others(5): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455680 | |||||||
| chr6:20455681 | G | C | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24165G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455681 | |||||||
| chr6:20455682 | T | C | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24164T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455682 | |||||||
| chr6:20455685 | T | A | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24161T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455685 | |||||||
| chr6:20455686 | T | G | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-24160T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455686 | |||||||
| chr6:20455852 | C | G | 2 | a0001c0001t0001g0252 a0001c0001t0005g0293 |
2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.394-23994C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20455852 | |||||||
| chr6:20456179 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0008g0003 a0001c0001t0008g0081 |
4 | HG00642.hp2 HG01081.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-23667G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456179 | |||||||
| chr6:20456278 | A | G | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-23568A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456278 | |||||||
| chr6:20456313 | TA | T | 11 | a0001c0001t0001g0191 a0001c0001t0001g0234 a0001c0001t0001g0254 others(8): Show |
11 | HG00323.hp1 HG01169.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.394-23517delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20456313 | ||||||
| chr6:20456460 | G | A | 87 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0050 others(84): Show |
88 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.394-23386G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456460 | |||||||
| chr6:20456547 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.394-23299G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456547 | |||||||
| chr6:20456641 | C | A | 1 | a0001c0001t0027g0036 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.394-23205C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456641 | |||||||
| chr6:20456671 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-23175T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456671 | |||||||
| chr6:20456696 | T | G | 2 | a0001c0001t0001g0252 a0001c0001t0005g0293 |
2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.394-23150T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456696 | |||||||
| chr6:20456869 | A | C | 2 | a0001c0001t0001g0252 a0001c0001t0005g0293 |
2 | HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.394-22977A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20456869 | |||||||
| chr6:20457241 | C | A | 1 | a0001c0001t0001g0324 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.394-22605C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457241 | |||||||
| chr6:20457261 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.394-22585G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457261 | |||||||
| chr6:20457268 | AG | A | 3 | a0001c0001t0005g0212 a0001c0001t0012g0065 a0001c0001t0013g0236 |
3 | HG02451.hp1 HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-22576delG | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20457268 | ||||||
| chr6:20457292 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0301 |
2 | HG02523.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.394-22554G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457292 | |||||||
| chr6:20457295 | C | G | 2 | a0001c0001t0001g0292 a0001c0001t0001g0305 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.394-22551C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457295 | |||||||
| chr6:20457348 | C | CT | 124 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(121): Show |
128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.394-22478dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20457348 | ||||||
| chr6:20457348 | C | CTT | 130 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0038 others(127): Show |
132 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.394-22479_394-2247 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20457348 | ||||||
| chr6:20457348 | C | CTTT | 16 | a0001c0001t0001g0030 a0001c0001t0001g0046 a0001c0001t0001g0139 others(13): Show |
16 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.394-22480_394-2247 others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20457348 | ||||||
| chr6:20457514 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394-22332G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457514 | |||||||
| chr6:20457596 | G | A | 74 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0046 others(71): Show |
75 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.394-22250G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457596 | |||||||
| chr6:20457612 | A | C | 2 | a0001c0001t0001g0097 a0001c0001t0003g0127 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.394-22234A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457612 | |||||||
| chr6:20457689 | C | A | 1 | a0001c0001t0001g0017 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.394-22157C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457689 | |||||||
| chr6:20457948 | C | T | 16 | a0001c0001t0001g0107 a0001c0001t0001g0116 a0001c0001t0001g0126 others(13): Show |
16 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.394-21898C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20457948 | |||||||
| chr6:20458074 | G | C | 1 | a0003c0003t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.394-21772G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458074 | |||||||
| chr6:20458294 | A | G | 19 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0107 others(16): Show |
20 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.394-21552A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458294 | |||||||
| chr6:20458475 | A | G | 16 | a0001c0001t0001g0107 a0001c0001t0001g0116 a0001c0001t0001g0126 others(13): Show |
16 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.394-21371A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458475 | |||||||
| chr6:20458830 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.394-21016C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458830 | |||||||
| chr6:20458845 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0003g0319 a0001c0001t0003g0323 |
3 | HG03098.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.394-21001G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458845 | |||||||
| chr6:20458951 | GT | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.394-20887delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20458951 | ||||||
| chr6:20458990 | G | A | 1 | a0001c0001t0007g0098 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.394-20856G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20458990 | |||||||
| chr6:20459137 | T | C | 3 | a0001c0001t0005g0212 a0001c0001t0012g0065 a0001c0001t0013g0236 |
3 | HG02451.hp1 HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-20709T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20459137 | |||||||
| chr6:20459141 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.394-20705C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20459141 | |||||||
| chr6:20459230 | C | T | 1 | a0004c0004t0001g0006 | 2 | HG02630.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.394-20616C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20459230 | |||||||
| chr6:20459442 | C | T | 279 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.394-20404C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20459442 | |||||||
| chr6:20460039 | T | C | 283 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.394-19807T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460039 | |||||||
| chr6:20460054 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0003g0127 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.394-19792C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460054 | |||||||
| chr6:20460072 | C | G | 4 | a0001c0001t0003g0108 a0001c0001t0003g0313 a0002c0002t0003g0091 others(1): Show |
4 | HG02622.hp1 NA19030.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-19774C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460072 | |||||||
| chr6:20460075 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-19771A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460075 | |||||||
| chr6:20460241 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394-19605A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460241 | |||||||
| chr6:20460465 | T | G | 284 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(281): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.394-19381T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460465 | |||||||
| chr6:20460552 | T | G | 1 | a0001c0001t0005g0212 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-19294T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460552 | |||||||
| chr6:20460563 | A | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394-19283A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460563 | |||||||
| chr6:20460656 | C | G | 1 | a0001c0001t0001g0271 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.394-19190C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460656 | |||||||
| chr6:20460678 | A | G | 8 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0042 others(5): Show |
8 | HG01069.hp2 HG01261.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-19168A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460678 | |||||||
| chr6:20460794 | G | A | 1 | a0001c0001t0014g0218 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.394-19052G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20460794 | |||||||
| chr6:20460996 | C | CA | 28 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0021 others(25): Show |
28 | HG00639.hp2 HG01081.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.394-18822dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20460996 | ||||||
| chr6:20460996 | CAAA | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0031 others(57): Show |
63 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.394-18824_394-1882 others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20460996 | ||||||
| chr6:20460996 | CAAAA | C | 207 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(204): Show |
209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.394-18825_394-1882 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20460996 | ||||||
| chr6:20460996 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-18831_394-1882 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20460996 | ||||||
| chr6:20460996 | CAAAAAAA others(9): Show |
C | 4 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0007g0329 others(1): Show |
4 | HG02451.hp2 HG02559.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-18837_394-1882 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20460996 | ||||||
| chr6:20461071 | T | C | 176 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0016 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.394-18775T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461071 | |||||||
| chr6:20461079 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.394-18767C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461079 | |||||||
| chr6:20461174 | A | G | 76 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0046 others(73): Show |
77 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.394-18672A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461174 | |||||||
| chr6:20461201 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0030 others(98): Show |
104 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.394-18645A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461201 | |||||||
| chr6:20461215 | C | T | 1 | a0001c0001t0016g0219 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.394-18631C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461215 | |||||||
| chr6:20461382 | C | T | 276 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(273): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.394-18464C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461382 | |||||||
| chr6:20461462 | C | G | 1 | a0001c0001t0001g0185 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.394-18384C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461462 | |||||||
| chr6:20461737 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-18109C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461737 | |||||||
| chr6:20461816 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.394-18030A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461816 | |||||||
| chr6:20461889 | G | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.394-17957G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461889 | |||||||
| chr6:20461907 | G | A | 279 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.394-17939G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20461907 | |||||||
| chr6:20462135 | A | G | 1 | a0001c0001t0002g0022 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.394-17711A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462135 | |||||||
| chr6:20462299 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.394-17547G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462299 | |||||||
| chr6:20462428 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.394-17418A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462428 | |||||||
| chr6:20462458 | CT | C | 19 | a0001c0001t0001g0097 a0001c0001t0001g0107 a0001c0001t0001g0116 others(16): Show |
19 | HG02109.hp2 HG02451.hp2 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.394-17373delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462458 | ||||||
| chr6:20462519 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0007g0098 |
3 | HG02559.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.394-17327G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462519 | |||||||
| chr6:20462672 | G | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0183 |
3 | HG01069.hp2 HG01261.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.394-17174G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462672 | |||||||
| chr6:20462738 | G | A | 1 | a0001c0001t0008g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.394-17108G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462738 | |||||||
| chr6:20462797 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.394-17049G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462797 | |||||||
| chr6:20462859 | CT | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0096 a0001c0001t0001g0120 others(4): Show |
7 | HG02055.hp1 HG03654.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-16950delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTT | C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0077 a0001c0001t0001g0121 others(7): Show |
10 | HG01243.hp2 HG01255.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.394-16951_394-1695 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTT | C | 12 | a0001c0001t0001g0062 a0001c0001t0001g0135 a0001c0001t0001g0310 others(9): Show |
13 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-16952_394-1695 others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTT | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0061 others(8): Show |
11 | HG00741.hp1 HG01496.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.394-16953_394-1695 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTTT | C | 23 | a0001c0001t0001g0033 a0001c0001t0001g0079 a0001c0001t0001g0088 others(20): Show |
25 | HG01109.hp1 HG01255.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.394-16954_394-1695 others(9): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTTTT | C | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(57): Show |
60 | HG00639.hp1 HG00642.hp1 HG00741.hp2 others(57): Show |
intron_variant | MODIFIER | c.394-16955_394-1695 others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTTTTT | C | 84 | a0001c0001t0001g0028 a0001c0001t0001g0040 a0001c0001t0001g0042 others(81): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.394-16956_394-1695 others(11): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0115 a0001c0001t0001g0187 others(6): Show |
9 | HG01069.hp2 HG01167.hp2 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-16957_394-1695 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTTTTT others(2): Show |
C | 65 | a0001c0001t0001g0030 a0001c0001t0001g0046 a0001c0001t0001g0049 others(62): Show |
66 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.394-16958_394-1695 others(13): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0001g0170 a0001c0001t0001g0182 a0001c0001t0001g0205 others(2): Show |
5 | HG01069.hp1 HG01167.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-16959_394-1695 others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0118 a0001c0001t0005g0212 |
2 | HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.394-16961_394-1695 others(16): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0001g0080 a0001c0001t0001g0119 a0001c0001t0001g0307 others(1): Show |
4 | HG02257.hp2 HG02809.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-16962_394-1695 others(17): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTTTTT others(10): Show |
C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0132 a0001c0001t0003g0319 others(1): Show |
4 | HG03098.hp2 HG03579.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-16966_394-1695 others(21): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462859 | CTTTTTTT others(12): Show |
C | 3 | a0001c0001t0001g0237 a0005c0005t0001g0147 a0005c0005t0004g0178 |
3 | HG02129.hp2 HG03942.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.394-16968_394-1695 others(23): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462859 | ||||||
| chr6:20462860 | T | TC | 6 | a0001c0001t0001g0002 a0001c0001t0001g0093 a0001c0001t0008g0003 others(3): Show |
7 | HG00642.hp2 HG01081.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-16986_394-1698 others(5): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462860 | |||||||
| chr6:20462861 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-16985T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462861 | |||||||
| chr6:20462862 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0093 a0001c0001t0002g0272 others(4): Show |
8 | HG00642.hp2 HG01081.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-16984T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462862 | |||||||
| chr6:20462863 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-16983T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462863 | |||||||
| chr6:20462864 | T | C | 4 | a0001c0001t0001g0093 a0001c0001t0002g0272 a0001c0001t0008g0003 others(1): Show |
5 | HG00642.hp2 HG01081.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-16982T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462864 | |||||||
| chr6:20462866 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0112 |
3 | HG02965.hp1 HG03516.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.394-16980T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462866 | |||||||
| chr6:20462889 | T | A | 2 | a0001c0001t0001g0242 a0001c0001t0002g0241 |
2 | HG01261.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.394-16957T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462889 | |||||||
| chr6:20462904 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.394-16942G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462904 | |||||||
| chr6:20462910 | A | T | 6 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-16936A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462910 | |||||||
| chr6:20462949 | G | T | 23 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0061 others(20): Show |
25 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.394-16897G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462949 | |||||||
| chr6:20462963 | T | A | 2 | a0001c0001t0001g0097 a0001c0001t0003g0127 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.394-16883T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20462963 | |||||||
| chr6:20462980 | T | TTTAGTGC others(9): Show |
9 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0310 others(6): Show |
9 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-16864_394-1684 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20462980 | ||||||
| chr6:20463020 | G | T | 1 | a0001c0001t0001g0031 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.394-16826G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463020 | |||||||
| chr6:20463068 | G | A | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-16778G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463068 | |||||||
| chr6:20463102 | G | C | 5 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-16744G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463102 | |||||||
| chr6:20463118 | T | C | 7 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-16728T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463118 | |||||||
| chr6:20463205 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.394-16641G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463205 | |||||||
| chr6:20463349 | G | A | 5 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-16497G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463349 | |||||||
| chr6:20463443 | C | G | 286 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.394-16403C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463443 | |||||||
| chr6:20463598 | A | G | 1 | a0001c0001t0006g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.394-16248A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463598 | |||||||
| chr6:20463733 | A | G | 8 | a0001c0001t0001g0063 a0001c0001t0001g0216 a0001c0001t0005g0004 others(5): Show |
9 | HG01175.hp1 HG01192.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-16113A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463733 | |||||||
| chr6:20463864 | C | A | 1 | a0001c0001t0002g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-15982C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463864 | |||||||
| chr6:20463993 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.394-15853C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20463993 | |||||||
| chr6:20464155 | G | A | 1 | a0001c0001t0008g0111 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.394-15691G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464155 | |||||||
| chr6:20464221 | A | G | 92 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0046 others(89): Show |
93 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.394-15625A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464221 | |||||||
| chr6:20464278 | C | T | 152 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0019 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.394-15568C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464278 | |||||||
| chr6:20464404 | G | C | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-15442G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464404 | |||||||
| chr6:20464405 | ATCTCTTA others(9): Show |
A | 1 | a0001c0001t0001g0174 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.394-15438_394-1542 others(20): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20464405 | ||||||
| chr6:20464407 | C | G | 7 | a0001c0001t0001g0080 a0001c0001t0001g0097 a0001c0001t0001g0118 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-15439C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464407 | |||||||
| chr6:20464644 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0235 |
2 | NA18948.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.394-15202G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464644 | |||||||
| chr6:20464658 | G | A | 7 | a0001c0001t0001g0080 a0001c0001t0001g0097 a0001c0001t0001g0118 others(4): Show |
7 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-15188G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464658 | |||||||
| chr6:20464773 | T | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | NA18951.hp1 NA19000.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.394-15073T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464773 | |||||||
| chr6:20464840 | G | A | 1 | a0003c0003t0001g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-15006G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464840 | |||||||
| chr6:20464957 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.394-14889C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464957 | |||||||
| chr6:20464975 | A | G | 1 | a0001c0001t0005g0212 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-14871A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464975 | |||||||
| chr6:20464976 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.394-14870G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20464976 | |||||||
| chr6:20465339 | T | A | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-14507T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465339 | |||||||
| chr6:20465394 | C | A | 3 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0008t0001g0160 |
3 | HG01081.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.394-14452C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465394 | |||||||
| chr6:20465633 | T | C | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.394-14213T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465633 | |||||||
| chr6:20465679 | T | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.394-14167T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465679 | |||||||
| chr6:20465738 | T | C | 11 | a0001c0001t0001g0067 a0001c0001t0001g0245 a0001c0001t0001g0254 others(8): Show |
12 | HG00544.hp2 HG02015.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.394-14108T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465738 | |||||||
| chr6:20465808 | C | CAT | 39 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0094 others(36): Show |
40 | HG01255.hp2 HG02109.hp2 HG02129.hp2 others(37): Show |
intron_variant | MODIFIER | c.394-14026_394-1402 others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20465808 | ||||||
| chr6:20465808 | C | CATAT | 3 | a0001c0001t0003g0108 a0001c0001t0003g0313 a0002c0002t0003g0091 |
3 | NA19030.hp1 NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.394-14028_394-1402 others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20465808 | ||||||
| chr6:20465884 | T | G | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-13962T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465884 | |||||||
| chr6:20465929 | G | T | 1 | a0003c0003t0001g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.394-13917G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20465929 | |||||||
| chr6:20466105 | G | C | 309 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(306): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.394-13741G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466105 | |||||||
| chr6:20466107 | T | A | 1 | a0001c0001t0001g0234 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.394-13739T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466107 | |||||||
| chr6:20466122 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 |
3 | NA18951.hp1 NA19000.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.394-13724C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466122 | |||||||
| chr6:20466129 | T | G | 309 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(306): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.394-13717T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466129 | |||||||
| chr6:20466270 | G | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0234 |
2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.394-13576G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466270 | |||||||
| chr6:20466305 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.394-13541G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466305 | |||||||
| chr6:20466685 | CT | C | 225 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(222): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.394-13146delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20466685 | ||||||
| chr6:20466751 | C | T | 3 | a0001c0001t0007g0329 a0001c0001t0025g0071 a0001c0001t0026g0328 |
3 | HG02451.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.394-13095C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466751 | |||||||
| chr6:20466764 | T | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(231): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.394-13082T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466764 | |||||||
| chr6:20466772 | T | C | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-13074T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466772 | |||||||
| chr6:20466773 | G | C | 309 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(306): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.394-13073G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466773 | |||||||
| chr6:20466780 | T | C | 3 | a0001c0001t0002g0161 a0001c0001t0004g0162 a0001c0001t0004g0167 |
3 | NA18946.hp1 NA18981.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.394-13066T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466780 | |||||||
| chr6:20466838 | C | T | 13 | a0001c0001t0001g0046 a0001c0001t0001g0149 a0001c0001t0001g0170 others(10): Show |
13 | HG01975.hp2 HG01978.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.394-13008C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466838 | |||||||
| chr6:20466908 | C | CTGACCTC others(1): Show |
3 | a0001c0001t0001g0060 a0001c0001t0001g0151 a0001c0001t0001g0269 |
3 | HG03704.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.394-12932_394-1292 others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20466908 | ||||||
| chr6:20466931 | T | C | 234 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(231): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.394-12915T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466931 | |||||||
| chr6:20466997 | C | T | 74 | a0001c0001t0001g0030 a0001c0001t0001g0046 a0001c0001t0001g0049 others(71): Show |
75 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.394-12849C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20466997 | |||||||
| chr6:20467132 | A | G | 234 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(231): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.394-12714A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467132 | |||||||
| chr6:20467150 | A | T | 1 | a0001c0001t0003g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.394-12696A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467150 | |||||||
| chr6:20467347 | G | A | 230 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.394-12499G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467347 | |||||||
| chr6:20467372 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-12474C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467372 | |||||||
| chr6:20467415 | A | G | 1 | a0001c0001t0005g0212 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-12431A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467415 | |||||||
| chr6:20467448 | G | C | 4 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0007g0109 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-12398G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467448 | |||||||
| chr6:20467540 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0003g0319 a0001c0001t0003g0323 |
3 | HG03098.hp2 NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.394-12306A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467540 | |||||||
| chr6:20467613 | G | A | 1 | a0001c0001t0005g0212 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-12233G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467613 | |||||||
| chr6:20467616 | G | C | 3 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02257.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.394-12230G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467616 | |||||||
| chr6:20467642 | T | A | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-12204T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467642 | |||||||
| chr6:20467837 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0135 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.394-12009T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467837 | |||||||
| chr6:20467863 | A | ATGCCACT others(20): Show |
6 | a0001c0001t0001g0030 a0001c0001t0001g0080 a0001c0001t0001g0118 others(3): Show |
6 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-11962_394-1193 others(31): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20467863 | ||||||
| chr6:20467876 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.394-11970C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20467876 | |||||||
| chr6:20468157 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0093 others(3): Show |
8 | HG00642.hp2 HG01081.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-11689G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468157 | |||||||
| chr6:20468239 | C | G | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0077 |
3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.394-11607C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468239 | |||||||
| chr6:20468243 | A | G | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0077 |
3 | HG01243.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.394-11603A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468243 | |||||||
| chr6:20468331 | C | T | 7 | a0001c0001t0001g0063 a0001c0001t0001g0216 a0001c0001t0005g0004 others(4): Show |
8 | HG01192.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-11515C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468331 | |||||||
| chr6:20468403 | G | A | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.394-11443G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468403 | |||||||
| chr6:20468404 | A | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(222): Show |
231 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.394-11442A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468404 | |||||||
| chr6:20468558 | T | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0046 others(72): Show |
76 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.394-11288T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468558 | |||||||
| chr6:20468674 | C | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0068 |
3 | HG02970.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394-11172C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468674 | |||||||
| chr6:20468737 | C | T | 38 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0094 others(35): Show |
39 | HG01255.hp2 HG02109.hp2 HG02129.hp2 others(36): Show |
intron_variant | MODIFIER | c.394-11109C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20468737 | |||||||
| chr6:20469014 | G | A | 2 | a0001c0001t0002g0179 a0001c0001t0011g0025 |
2 | HG00639.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.394-10832G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469014 | |||||||
| chr6:20469052 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.394-10794T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469052 | |||||||
| chr6:20469101 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.394-10745C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469101 | |||||||
| chr6:20469270 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.394-10576A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469270 | |||||||
| chr6:20469475 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0005g0290 |
2 | HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.394-10371A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469475 | |||||||
| chr6:20469531 | G | A | 324 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(321): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.394-10315G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469531 | |||||||
| chr6:20469670 | A | C | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG00140.hp1 HG00280.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-10176A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20469670 | |||||||
| chr6:20470094 | A | G | 1 | a0001c0001t0005g0212 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-9752A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470094 | |||||||
| chr6:20470115 | C | T | 4 | a0001c0001t0001g0310 a0001c0001t0001g0312 a0001c0001t0003g0309 others(1): Show |
4 | HG01884.hp1 HG02280.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.394-9731C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470115 | |||||||
| chr6:20470288 | T | C | 1 | a0001c0001t0001g0019 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.394-9558T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470288 | |||||||
| chr6:20470426 | A | G | 9 | a0001c0001t0001g0107 a0001c0001t0003g0086 a0001c0001t0003g0087 others(6): Show |
9 | HG02109.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-9420A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470426 | |||||||
| chr6:20470562 | GAT | G | 5 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-9283_394-9282d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470562 | |||||||
| chr6:20470676 | C | G | 1 | a0001c0001t0013g0236 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.394-9170C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470676 | |||||||
| chr6:20470677 | A | C | 179 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(176): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.394-9169A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470677 | |||||||
| chr6:20470699 | T | G | 179 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(176): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.394-9147T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470699 | |||||||
| chr6:20470724 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.394-9122T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470724 | |||||||
| chr6:20470918 | A | G | 1 | a0003c0003t0001g0070 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.394-8928A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20470918 | |||||||
| chr6:20471130 | T | G | 1 | a0001c0001t0001g0245 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.394-8716T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471130 | |||||||
| chr6:20471304 | C | T | 4 | a0001c0001t0001g0220 a0001c0001t0001g0256 a0001c0001t0002g0130 others(1): Show |
4 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.394-8542C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471304 | |||||||
| chr6:20471311 | G | T | 15 | a0001c0001t0001g0055 a0001c0001t0001g0207 a0001c0001t0001g0209 others(12): Show |
15 | NA18612.hp1 NA18950.hp2 NA18955.hp1 others(12): Show |
intron_variant | MODIFIER | c.394-8535G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471311 | |||||||
| chr6:20471348 | C | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0093 others(3): Show |
8 | HG00642.hp2 HG01081.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-8498C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471348 | |||||||
| chr6:20471359 | C | T | 5 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-8487C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471359 | |||||||
| chr6:20471459 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.394-8387G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471459 | |||||||
| chr6:20471516 | G | A | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0094 others(19): Show |
22 | HG01255.hp2 HG02129.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.394-8330G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471516 | |||||||
| chr6:20471569 | G | A | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-8277G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471569 | |||||||
| chr6:20471768 | T | C | 309 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(306): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.394-8078T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20471768 | |||||||
| chr6:20472024 | C | A | 1 | a0001c0001t0002g0223 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.394-7822C>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472024 | |||||||
| chr6:20472025 | A | AAC | 51 | a0001c0001t0001g0035 a0001c0001t0001g0061 a0001c0001t0001g0062 others(48): Show |
52 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.394-7778_394-7777d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | A | AACAC | 38 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0029 others(35): Show |
38 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.394-7780_394-7777d others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | A | AACACAC | 31 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0040 others(28): Show |
33 | HG00408.hp1 HG00741.hp1 HG01192.hp2 others(30): Show |
intron_variant | MODIFIER | c.394-7782_394-7777d others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | A | AACACACA others(1): Show |
38 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0038 others(35): Show |
38 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.394-7784_394-7777d others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | A | AACACACA others(3): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0096 a0001c0001t0001g0292 others(4): Show |
7 | HG01496.hp1 HG01516.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.394-7786_394-7777d others(12): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | A | AACACACA others(5): Show |
1 | a0001c0001t0001g0042 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.394-7788_394-7777d others(14): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | A | AACACACA others(7): Show |
1 | a0001c0001t0001g0021 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.394-7790_394-7777d others(16): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | AAC | A | 48 | a0001c0001t0001g0002 a0001c0001t0001g0041 a0001c0001t0001g0046 others(45): Show |
49 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.394-7778_394-7777d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | AACAC | A | 67 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0023 others(64): Show |
68 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.394-7780_394-7777d others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | AACACAC | A | 9 | a0001c0001t0001g0145 a0001c0001t0001g0283 a0001c0001t0002g0229 others(6): Show |
9 | HG00438.hp2 HG02451.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.394-7782_394-7777d others(8): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | AACACACA others(1): Show |
A | 8 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0089 others(5): Show |
8 | HG02486.hp1 HG03516.hp1 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.394-7784_394-7777d others(10): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472025 | AACACACA others(7): Show |
A | 1 | a0001c0001t0002g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.394-7790_394-7777d others(16): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472025 | ||||||
| chr6:20472070 | T | A | 3 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0014 |
3 | HG02572.hp2 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.394-7776T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472070 | |||||||
| chr6:20472126 | A | T | 2 | a0001c0001t0003g0122 a0001c0001t0003g0123 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.394-7720A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472126 | |||||||
| chr6:20472159 | AAAAT | A | 176 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0016 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.394-7680_394-7677d others(6): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20472159 | ||||||
| chr6:20472471 | G | A | 1 | a0003c0003t0001g0117 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.394-7375G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472471 | |||||||
| chr6:20472504 | T | C | 2 | a0001c0001t0003g0124 a0001c0001t0003g0320 |
2 | HG02258.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.394-7342T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472504 | |||||||
| chr6:20472511 | A | G | 23 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0094 others(20): Show |
23 | HG01255.hp2 HG02129.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.394-7335A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472511 | |||||||
| chr6:20472606 | C | T | 10 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0135 others(7): Show |
10 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-7240C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472606 | |||||||
| chr6:20472842 | T | G | 318 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(315): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.394-7004T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20472842 | |||||||
| chr6:20473006 | G | C | 1 | a0001c0001t0001g0325 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.394-6840G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473006 | |||||||
| chr6:20473218 | A | G | 1 | a0001c0001t0011g0025 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.394-6628A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473218 | |||||||
| chr6:20473312 | A | G | 2 | a0001c0001t0002g0130 a0001c0001t0002g0131 |
2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.394-6534A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473312 | |||||||
| chr6:20473441 | A | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0112 |
2 | HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.394-6405A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473441 | |||||||
| chr6:20473533 | G | GT | 3 | a0001c0001t0005g0212 a0001c0001t0012g0065 a0001c0001t0013g0236 |
3 | HG02451.hp1 HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-6312dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20473533 | ||||||
| chr6:20473626 | G | A | 176 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0016 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.394-6220G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473626 | |||||||
| chr6:20473654 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-6192C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20473654 | |||||||
| chr6:20474095 | T | TG | 4 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0249 others(1): Show |
5 | HG02970.hp2 HG03139.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-5749dupG | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20474095 | ||||||
| chr6:20474097 | G | GT | 300 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(297): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.394-5741dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20474097 | ||||||
| chr6:20474243 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-5603T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474243 | |||||||
| chr6:20474387 | C | T | 23 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0094 others(20): Show |
24 | HG01255.hp2 HG02129.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-5459C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474387 | |||||||
| chr6:20474536 | A | G | 23 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0094 others(20): Show |
24 | HG01255.hp2 HG02129.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.394-5310A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474536 | |||||||
| chr6:20474541 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0019g0208 |
2 | NA18956.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.394-5305G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474541 | |||||||
| chr6:20474570 | C | T | 5 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-5276C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474570 | |||||||
| chr6:20474666 | C | T | 25 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0094 others(22): Show |
26 | HG01255.hp2 HG02129.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-5180C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474666 | |||||||
| chr6:20474799 | T | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0093 others(3): Show |
8 | HG00642.hp2 HG01081.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-5047T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474799 | |||||||
| chr6:20474914 | G | A | 1 | a0001c0001t0025g0071 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.394-4932G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20474914 | |||||||
| chr6:20475144 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.394-4702T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20475144 | |||||||
| chr6:20475272 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.394-4574G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20475272 | |||||||
| chr6:20475772 | C | T | 1 | a0001c0001t0002g0246 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.394-4074C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20475772 | |||||||
| chr6:20475970 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.394-3876C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20475970 | |||||||
| chr6:20476052 | A | G | 2 | a0001c0001t0004g0173 a0001c0001t0004g0238 |
2 | NA18940.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.394-3794A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476052 | |||||||
| chr6:20476137 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.394-3709C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476137 | |||||||
| chr6:20476147 | G | A | 1 | a0001c0001t0005g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.394-3699G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476147 | |||||||
| chr6:20476243 | C | T | 20 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0094 others(17): Show |
21 | HG01255.hp2 HG02129.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.394-3603C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476243 | |||||||
| chr6:20476274 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.394-3572G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476274 | |||||||
| chr6:20476296 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.394-3550G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476296 | |||||||
| chr6:20476303 | G | A | 5 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
5 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.394-3543G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476303 | |||||||
| chr6:20476357 | C | T | 8 | a0001c0001t0001g0116 a0001c0001t0001g0126 a0001c0001t0003g0108 others(5): Show |
8 | HG02622.hp1 HG02970.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.394-3489C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476357 | |||||||
| chr6:20476365 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.394-3481C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476365 | |||||||
| chr6:20476372 | CA | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0093 others(11): Show |
16 | HG00642.hp2 HG01081.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.394-3462delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20476372 | ||||||
| chr6:20476385 | T | C | 1 | a0001c0001t0001g0285 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.394-3461T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476385 | |||||||
| chr6:20476663 | A | T | 24 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0061 others(21): Show |
26 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.394-3183A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20476663 | |||||||
| chr6:20477179 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-2667G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477179 | |||||||
| chr6:20477423 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | NA18953.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.394-2423T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477423 | |||||||
| chr6:20477448 | G | A | 2 | a0003c0003t0001g0070 a0003c0003t0001g0117 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-2398G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477448 | |||||||
| chr6:20477734 | C | T | 1 | a0004c0004t0007g0321 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.394-2112C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477734 | |||||||
| chr6:20477752 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.394-2094G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477752 | |||||||
| chr6:20477934 | G | A | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-1912G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20477934 | |||||||
| chr6:20478030 | CA | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0017 others(47): Show |
55 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.394-1803delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20478030 | ||||||
| chr6:20478030 | CAA | C | 14 | a0001c0001t0001g0080 a0001c0001t0001g0116 a0001c0001t0001g0118 others(11): Show |
14 | HG02257.hp2 HG02622.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.394-1804_394-1803d others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr6 | 20478030 | ||||||
| chr6:20478223 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0093 others(4): Show |
9 | HG00642.hp2 HG01081.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.394-1623G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478223 | |||||||
| chr6:20478414 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.394-1432G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478414 | |||||||
| chr6:20478499 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.394-1347G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478499 | |||||||
| chr6:20478678 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.394-1168G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478678 | |||||||
| chr6:20478936 | A | G | 7 | a0001c0001t0001g0097 a0001c0001t0001g0107 a0001c0001t0003g0086 others(4): Show |
7 | HG02109.hp2 HG02622.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.394-910A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478936 | |||||||
| chr6:20478983 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.394-863G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20478983 | |||||||
| chr6:20479036 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.394-810C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479036 | |||||||
| chr6:20479062 | T | C | 1 | a0001c0001t0014g0218 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.394-784T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479062 | |||||||
| chr6:20479072 | A | G | 10 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0135 others(7): Show |
10 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.394-774A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479072 | |||||||
| chr6:20479096 | T | G | 2 | a0003c0003t0001g0070 a0003c0003t0001g0117 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.394-750T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479096 | |||||||
| chr6:20479153 | T | G | 1 | a0002c0002t0001g0076 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.394-693T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479153 | |||||||
| chr6:20479204 | A | G | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.394-642A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479204 | |||||||
| chr6:20479251 | G | A | 1 | a0001c0001t0005g0212 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-595G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479251 | |||||||
| chr6:20479352 | T | G | 6 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.394-494T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479352 | |||||||
| chr6:20479415 | G | A | 1 | a0001c0001t0005g0212 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.394-431G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479415 | |||||||
| chr6:20479486 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.394-360G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479486 | |||||||
| chr6:20479510 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.394-336C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479510 | |||||||
| chr6:20479682 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.394-164C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 1/6 | chr6 | 20479682 | |||||||
| chr6:20480355 | A | G | 88 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0038 others(85): Show |
89 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.505+398A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480355 | |||||||
| chr6:20480360 | G | A | 22 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0061 others(19): Show |
24 | HG00741.hp1 HG01109.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.505+403G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480360 | |||||||
| chr6:20480404 | C | T | 1 | a0001c0001t0005g0294 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.505+447C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480404 | |||||||
| chr6:20480776 | CTGTT | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0084 others(9): Show |
13 | HG02258.hp2 HG02486.hp1 HG02896.hp2 others(10): Show |
intron_variant | MODIFIER | c.506-428_506-425del others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr6 | 20480776 | ||||||
| chr6:20480808 | G | A | 1 | a0001c0001t0005g0294 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.506-398G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480808 | |||||||
| chr6:20480909 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.506-297A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480909 | |||||||
| chr6:20480974 | A | C | 1 | a0001c0001t0001g0188 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.506-232A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480974 | |||||||
| chr6:20480990 | A | G | 2 | a0001c0001t0012g0065 a0001c0001t0013g0236 |
2 | HG03834.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.506-216A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20480990 | |||||||
| chr6:20481041 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.506-165A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20481041 | |||||||
| chr6:20481055 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0008g0003 a0001c0001t0008g0081 |
4 | HG00642.hp2 HG01081.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.506-151C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 2/6 | chr6 | 20481055 | |||||||
| chr6:20481447 | G | C | 19 | a0001c0001t0001g0015 a0001c0001t0001g0028 a0001c0001t0001g0029 others(16): Show |
19 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.725+22G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481447 | |||||||
| chr6:20481518 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.725+93C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481518 | |||||||
| chr6:20481594 | T | C | 265 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(262): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.725+169T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481594 | |||||||
| chr6:20481671 | C | T | 2 | a0001c0001t0008g0069 a0001c0001t0008g0111 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.725+246C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481671 | |||||||
| chr6:20481708 | A | C | 2 | a0001c0001t0002g0171 a0001c0001t0002g0176 |
2 | NA19011.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.725+283A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481708 | |||||||
| chr6:20481962 | G | A | 9 | a0001c0001t0001g0046 a0001c0001t0001g0149 a0001c0001t0001g0186 others(6): Show |
9 | HG01978.hp1 HG02148.hp2 NA18943.hp1 others(6): Show |
intron_variant | MODIFIER | c.725+537G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481962 | |||||||
| chr6:20481981 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0305 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.725+556G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20481981 | |||||||
| chr6:20482098 | T | C | 1 | a0001c0001t0003g0313 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.726-664T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482098 | |||||||
| chr6:20482104 | G | A | 255 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(252): Show |
260 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.726-658G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482104 | |||||||
| chr6:20482180 | G | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(138): Show |
144 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.726-582G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482180 | |||||||
| chr6:20482222 | C | T | 1 | a0001c0001t0005g0212 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.726-540C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482222 | |||||||
| chr6:20482342 | G | GT | 62 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(59): Show |
63 | HG00639.hp2 HG00741.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.726-405dupT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482342 | ||||||
| chr6:20482342 | G | GTT | 8 | a0001c0001t0001g0094 a0001c0001t0001g0164 a0001c0001t0001g0287 others(5): Show |
8 | HG01243.hp1 HG02280.hp1 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.726-406_726-405dup others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482342 | ||||||
| chr6:20482342 | GT | G | 41 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(38): Show |
42 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.726-405delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482342 | ||||||
| chr6:20482350 | T | G | 2 | a0002c0002t0001g0074 a0002c0002t0001g0075 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.726-412T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482350 | |||||||
| chr6:20482590 | G | GA | 14 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0041 others(11): Show |
14 | HG01192.hp1 HG01361.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.726-162dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482590 | ||||||
| chr6:20482590 | G | GAA | 35 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(32): Show |
35 | HG01167.hp2 HG01243.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.726-163_726-162dup others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482590 | ||||||
| chr6:20482590 | GAA | G | 22 | a0001c0001t0001g0326 a0001c0001t0002g0022 a0001c0001t0002g0037 others(19): Show |
22 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.726-163_726-162del others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482590 | ||||||
| chr6:20482597 | A | AAT | 8 | a0001c0001t0001g0139 a0001c0001t0001g0204 a0001c0001t0001g0205 others(5): Show |
8 | HG00280.hp1 HG00738.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.726-164_726-163ins others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482597 | ||||||
| chr6:20482597 | A | T | 12 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0285 others(9): Show |
12 | HG01943.hp1 HG02083.hp2 NA18970.hp2 others(9): Show |
intron_variant | MODIFIER | c.726-165A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482597 | |||||||
| chr6:20482599 | A | AAT | 5 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0291 others(2): Show |
5 | HG01071.hp2 HG01192.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.726-142_726-141dup others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482599 | ||||||
| chr6:20482599 | A | AATAT | 5 | a0001c0001t0001g0133 a0001c0001t0001g0175 a0001c0001t0001g0269 others(2): Show |
5 | HG00639.hp2 HG01891.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-144_726-141dup others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482599 | ||||||
| chr6:20482599 | A | T | 62 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0050 others(59): Show |
64 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.726-163A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482599 | |||||||
| chr6:20482599 | AAT | A | 67 | a0001c0001t0001g0007 a0001c0001t0001g0038 a0001c0001t0001g0042 others(64): Show |
69 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.726-142_726-141del others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482599 | ||||||
| chr6:20482599 | AATAT | A | 5 | a0001c0001t0003g0309 a0001c0001t0003g0323 a0001c0001t0005g0212 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-144_726-141del others(4): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482599 | ||||||
| chr6:20482600 | AT | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0084 others(20): Show |
25 | HG00642.hp2 HG01081.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.726-161delT | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482600 | |||||||
| chr6:20482600 | ATAT | A | 6 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(3): Show |
6 | HG02257.hp2 HG02258.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.726-161_726-159del others(3): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482600 | |||||||
| chr6:20482601 | T | A | 39 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(36): Show |
39 | HG01109.hp2 HG01978.hp1 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.726-161T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482601 | |||||||
| chr6:20482603 | T | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0079 others(22): Show |
27 | HG00642.hp2 HG01081.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.726-159T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482603 | |||||||
| chr6:20482605 | T | A | 8 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0089 others(5): Show |
8 | HG02055.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.726-157T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482605 | |||||||
| chr6:20482620 | A | ATG | 24 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(21): Show |
24 | HG00323.hp2 HG00738.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.726-138_726-137dup others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr6 | 20482620 | ||||||
| chr6:20482620 | A | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0017 others(21): Show |
26 | HG00140.hp1 HG01081.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.726-142A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 3/6 | chr6 | 20482620 | |||||||
| chr6:20482959 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0003g0014 |
2 | HG02572.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.884+39T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20482959 | |||||||
| chr6:20482999 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.884+79A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20482999 | |||||||
| chr6:20483045 | C | G | 1 | a0001c0001t0001g0020 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.884+125C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483045 | |||||||
| chr6:20483055 | ATG | A | 5 | a0001c0001t0003g0108 a0001c0001t0003g0309 a0001c0001t0003g0313 others(2): Show |
5 | HG02280.hp1 HG02451.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.884+148_884+149del others(2): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 20483055 | ||||||
| chr6:20483072 | C | T | 27 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0043 others(24): Show |
27 | HG01069.hp2 HG01261.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.884+152C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483072 | |||||||
| chr6:20483119 | T | C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG01167.hp2 HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.884+199T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483119 | |||||||
| chr6:20483129 | G | A | 1 | a0001c0001t0005g0078 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.884+209G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483129 | |||||||
| chr6:20483176 | C | T | 30 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.884+256C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483176 | |||||||
| chr6:20483277 | A | G | 1 | a0001c0001t0002g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.884+357A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483277 | |||||||
| chr6:20483339 | C | T | 11 | a0001c0001t0001g0055 a0001c0001t0001g0207 a0001c0001t0001g0209 others(8): Show |
11 | NA18612.hp1 NA18955.hp1 NA18956.hp1 others(8): Show |
intron_variant | MODIFIER | c.884+419C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483339 | |||||||
| chr6:20483372 | C | T | 9 | a0001c0001t0001g0063 a0001c0001t0001g0142 a0001c0001t0001g0164 others(6): Show |
9 | HG01071.hp2 HG01192.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.884+452C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483372 | |||||||
| chr6:20483483 | A | G | 2 | a0001c0001t0008g0069 a0001c0001t0008g0111 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.884+563A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483483 | |||||||
| chr6:20483490 | A | G | 1 | a0001c0001t0017g0306 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.884+570A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483490 | |||||||
| chr6:20483539 | A | G | 27 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0043 others(24): Show |
27 | HG01069.hp2 HG01261.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.884+619A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483539 | |||||||
| chr6:20483664 | C | T | 1 | a0001c0001t0023g0137 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.884+744C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483664 | |||||||
| chr6:20483777 | C | G | 1 | a0001c0001t0010g0222 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.884+857C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483777 | |||||||
| chr6:20483973 | C | T | 1 | a0001c0001t0016g0219 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.884+1053C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20483973 | |||||||
| chr6:20484024 | T | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0097 others(7): Show |
11 | HG02055.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.884+1104T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484024 | |||||||
| chr6:20484041 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.884+1121A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484041 | |||||||
| chr6:20484079 | T | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0067 a0001c0001t0001g0245 others(1): Show |
4 | NA18948.hp2 NA18956.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.884+1159T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484079 | |||||||
| chr6:20484182 | G | C | 1 | a0001c0001t0021g0104 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.884+1262G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484182 | |||||||
| chr6:20484378 | T | C | 2 | a0001c0001t0008g0069 a0001c0001t0008g0111 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.884+1458T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484378 | |||||||
| chr6:20484482 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.884+1562G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484482 | |||||||
| chr6:20484498 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.884+1578C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484498 | |||||||
| chr6:20484735 | C | T | 1 | a0001c0001t0016g0219 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.884+1815C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484735 | |||||||
| chr6:20484846 | G | C | 80 | a0001c0001t0001g0007 a0001c0001t0001g0030 a0001c0001t0001g0035 others(77): Show |
82 | HG00438.hp2 HG00544.hp2 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.885-1843G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484846 | |||||||
| chr6:20484858 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0026g0328 |
2 | HG00741.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.885-1831C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20484858 | |||||||
| chr6:20484952 | C | CA | 27 | a0001c0001t0001g0010 a0001c0001t0001g0121 a0001c0001t0001g0125 others(24): Show |
27 | HG00280.hp2 HG01255.hp1 HG01496.hp1 others(24): Show |
intron_variant | MODIFIER | c.885-1720dupA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 20484952 | ||||||
| chr6:20484952 | CA | C | 25 | a0001c0001t0001g0055 a0001c0001t0001g0062 a0001c0001t0001g0194 others(22): Show |
26 | HG00642.hp2 HG00738.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.885-1720delA | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr6 | 20484952 | ||||||
| chr6:20485124 | T | A | 3 | a0003c0003t0001g0070 a0003c0003t0001g0117 a0003c0003t0001g0146 |
3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-1565T>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485124 | |||||||
| chr6:20485146 | C | T | 1 | a0001c0001t0003g0313 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.885-1543C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485146 | |||||||
| chr6:20485230 | T | C | 3 | a0003c0003t0001g0070 a0003c0003t0001g0117 a0003c0003t0001g0146 |
3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-1459T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485230 | |||||||
| chr6:20485235 | T | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0126 others(6): Show |
9 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.885-1454T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485235 | |||||||
| chr6:20485313 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.885-1376C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485313 | |||||||
| chr6:20485389 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.885-1300G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485389 | |||||||
| chr6:20485400 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(250): Show |
260 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.885-1289A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485400 | |||||||
| chr6:20485440 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.885-1249T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485440 | |||||||
| chr6:20485441 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.885-1248G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485441 | |||||||
| chr6:20485534 | G | C | 2 | a0001c0001t0003g0087 a0001c0001t0003g0127 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.885-1155G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485534 | |||||||
| chr6:20485633 | T | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(76): Show |
83 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.885-1056T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485633 | |||||||
| chr6:20485667 | C | T | 31 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(28): Show |
33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.885-1022C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485667 | |||||||
| chr6:20485712 | A | T | 3 | a0003c0003t0001g0070 a0003c0003t0001g0117 a0003c0003t0001g0146 |
3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-977A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485712 | |||||||
| chr6:20485736 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.885-953C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485736 | |||||||
| chr6:20485800 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0028g0110 |
3 | HG02572.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.885-889A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20485800 | |||||||
| chr6:20486083 | C | T | 1 | a0001c0001t0009g0274 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.885-606C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486083 | |||||||
| chr6:20486178 | G | A | 1 | a0001c0001t0004g0238 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.885-511G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486178 | |||||||
| chr6:20486260 | T | G | 6 | a0001c0001t0003g0008 a0001c0001t0003g0009 a0001c0001t0003g0124 others(3): Show |
6 | HG02109.hp1 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.885-429T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486260 | |||||||
| chr6:20486275 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(192): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.885-414A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486275 | |||||||
| chr6:20486334 | G | A | 125 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(122): Show |
127 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.885-355G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486334 | |||||||
| chr6:20486335 | C | T | 1 | a0001c0001t0008g0069 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.885-354C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486335 | |||||||
| chr6:20486343 | T | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0013 others(46): Show |
51 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.885-346T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486343 | |||||||
| chr6:20486383 | C | T | 12 | a0001c0001t0001g0080 a0001c0001t0001g0092 a0001c0001t0001g0113 others(9): Show |
12 | HG01167.hp2 HG01256.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.885-306C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486383 | |||||||
| chr6:20486384 | G | A | 3 | a0003c0003t0001g0070 a0003c0003t0001g0117 a0003c0003t0001g0146 |
3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-305G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486384 | |||||||
| chr6:20486387 | C | T | 3 | a0003c0003t0001g0070 a0003c0003t0001g0117 a0003c0003t0001g0146 |
3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-302C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486387 | |||||||
| chr6:20486398 | G | A | 3 | a0003c0003t0001g0070 a0003c0003t0001g0117 a0003c0003t0001g0146 |
3 | HG02622.hp1 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.885-291G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486398 | |||||||
| chr6:20486473 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.885-216C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486473 | |||||||
| chr6:20486521 | C | T | 1 | a0001c0001t0026g0328 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.885-168C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486521 | |||||||
| chr6:20486523 | C | T | 124 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(121): Show |
126 | HG00438.hp2 HG00544.hp2 HG00738.hp2 others(123): Show |
intron_variant | MODIFIER | c.885-166C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486523 | |||||||
| chr6:20486563 | C | T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0073 others(9): Show |
12 | HG01081.hp1 HG01361.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.885-126C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486563 | |||||||
| chr6:20486567 | C | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0015 others(19): Show |
23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.885-122C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486567 | |||||||
| chr6:20486604 | T | G | 1 | a0001c0001t0021g0104 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.885-85T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486604 | |||||||
| chr6:20486647 | T | C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG01167.hp2 HG02145.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.885-42T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 4/6 | chr6 | 20486647 | |||||||
| chr6:20487019 | T | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(194): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.999+216T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487019 | |||||||
| chr6:20487038 | C | T | 2 | a0001c0001t0003g0008 a0001c0001t0003g0009 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.999+235C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487038 | |||||||
| chr6:20487138 | G | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0028g0110 |
3 | HG02572.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.999+335G>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487138 | |||||||
| chr6:20487343 | T | G | 12 | a0001c0001t0004g0053 a0001c0001t0004g0058 a0001c0001t0004g0162 others(9): Show |
12 | HG02040.hp1 HG02129.hp2 HG03654.hp2 others(9): Show |
intron_variant | MODIFIER | c.999+540T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487343 | |||||||
| chr6:20487346 | A | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0012 others(194): Show |
204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.999+543A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487346 | |||||||
| chr6:20487366 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0073 others(9): Show |
12 | HG01081.hp1 HG01361.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.999+563G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487366 | |||||||
| chr6:20487388 | G | T | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.999+585G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487388 | |||||||
| chr6:20487410 | G | A | 7 | a0001c0001t0007g0098 a0001c0001t0007g0102 a0001c0001t0007g0103 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.999+607G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487410 | |||||||
| chr6:20487922 | A | G | 33 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0085 others(30): Show |
33 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.1000-191A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487922 | |||||||
| chr6:20487960 | A | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0253 |
2 | HG02074.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1000-153A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20487960 | |||||||
| chr6:20488003 | G | A | 126 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(123): Show |
128 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(125): Show |
intron_variant | MODIFIER | c.1000-110G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20488003 | |||||||
| chr6:20488009 | G | A | 4 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0128 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-104G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 5/6 | chr6 | 20488009 | |||||||
| chr6:20488424 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0064 |
2 | NA19001.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1135+176G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488424 | |||||||
| chr6:20488542 | G | A | 1 | a0001c0001t0003g0014 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1135+294G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488542 | |||||||
| chr6:20488656 | T | C | 40 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0038 others(37): Show |
41 | HG01069.hp2 HG01081.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.1135+408T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488656 | |||||||
| chr6:20488663 | C | G | 28 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0016 others(25): Show |
30 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.1135+415C>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488663 | |||||||
| chr6:20488666 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0015 others(193): Show |
202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.1135+418A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488666 | |||||||
| chr6:20488678 | G | A | 6 | a0001c0001t0001g0079 a0001c0001t0001g0121 a0001c0001t0023g0137 others(3): Show |
6 | HG02622.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1135+430G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488678 | |||||||
| chr6:20488886 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1135+638C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488886 | |||||||
| chr6:20488956 | G | T | 4 | a0001c0001t0003g0001 a0001c0001t0003g0014 a0001c0001t0003g0323 others(1): Show |
6 | HG01255.hp1 HG02572.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.1135+708G>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488956 | |||||||
| chr6:20488990 | T | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0217 |
2 | HG02155.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1135+742T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20488990 | |||||||
| chr6:20488994 | A | AAAAAG | 9 | a0001c0001t0001g0010 a0001c0001t0001g0125 a0001c0001t0001g0126 others(6): Show |
9 | HG01496.hp1 HG01884.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1135+765_1135+769d others(7): Show |
E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr6 | 20488994 | ||||||
| chr6:20489142 | A | C | 1 | a0001c0001t0003g0001 | 3 | HG03471.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1135+894A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489142 | |||||||
| chr6:20489144 | G | A | 3 | a0001c0001t0001g0079 a0001c0001t0001g0121 a0001c0001t0023g0137 |
3 | HG02630.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1135+896G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489144 | |||||||
| chr6:20489272 | A | G | 3 | a0001c0001t0004g0058 a0001c0001t0004g0267 a0001c0001t0004g0268 |
3 | HG03654.hp2 HG03688.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1136-896A>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489272 | |||||||
| chr6:20489386 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1136-782C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489386 | |||||||
| chr6:20489391 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1136-777A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489391 | |||||||
| chr6:20489432 | A | C | 127 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0020 others(124): Show |
129 | HG00438.hp2 HG00544.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.1136-736A>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489432 | |||||||
| chr6:20489463 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1136-705C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489463 | |||||||
| chr6:20489539 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1136-629T>C | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489539 | |||||||
| chr6:20489950 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1136-218A>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489950 | |||||||
| chr6:20489983 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1136-185G>A | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20489983 | |||||||
| chr6:20490035 | C | T | 4 | a0001c0001t0001g0080 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG02257.hp2 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136-133C>T | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20490035 | |||||||
| chr6:20490159 | T | G | 27 | a0001c0001t0001g0079 a0001c0001t0001g0084 a0001c0001t0001g0085 others(24): Show |
27 | HG01109.hp1 HG01884.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.1136-9T>G | E2F3 | ENSG00000112242.16 | transcript | ENST00000346618.8 | protein_coding | 6/6 | chr6 | 20490159 |